Journal List > Blood Res > v.56(S1) > 1148618

Nekoukar, Moghimi, and Salehifar: A narrative review on adverse effects of dasatinib with a focus on pharmacotherapy of dasatinib-induced pulmonary toxicities

Abstract

Chronic myeloid leukemia (CML), a myeloproliferative disorder caused by the over activity of BCR-ABL1 (breakpoint cluster region-Abelson), has been successfully treated by Tyrosine kinase inhibitors (TKIs). While imatinib is known as the first-line treatment of CML, in some cases other TKIs including dasatinib, nilotinib, bosutinib, and ponatinib may be preferred. Dasatinib, a second-generation TKI, inhibits multiple family kinases including BCR-ABL, SRC family kinases, receptor kinases, and TEC family kinases. It is effective against most imatinib-resistant cases except T315I mutation. Despite the superiority of dasatinib in its hematologic and cytogenetic responses in CML compared to imatinib, its potentially harmful pulmonary complications including pleural effusion (PE) and pulmonary arterial hypertension (PAH) may limit its use. Appropriate management of these serious adverse reactions is critical in both improving the quality of life and the outcome of the patient. In this narrative review, we will scrutinize the pulmonary complications of dasatinib and focus on the management of these toxicities.

INTRODUCTION

An overview to CML

Chronic myeloid leukemia (CML) is a myeloproliferative disorder associated with Philadelphia chromosome t (9;22)(q34;q11) and/or the BCR-ABL1 (breakpoint cluster Region-Abelson) fusion gene. Cytogenetic abnormality results in the expression of BCR-ABL1 protein with a constitutive tyrosine kinase (TK) activity. The incidence of CML is one to two cases per 100,000 adults [1, 2].
BCR-ABL1 promotes cell proliferation by downstream pathways like MYC, STAT, RAS, RAF and JUN kinases [2]. Although it can occur at any age, the median age of patients is 67 years [3].
The disease is defined as 3 phases: chronic phase (CP), accelerated phase (AP), and blast phase (BP). Uncontrolled chronic phase will lead to accelerated and blast phases of CML within 3 to 5 years [3]. The diagnosis of CML is based on the detection of the Philadelphia chromosome, the BCR-ABL1 fusion gene or the BCR-ABL1 fusion mRNA by conventional cytogenetics, fluorescence in situ hybridization (FISH) analysis or reverse transcriptase polymerase chain reaction (RT-PCR) on peripheral blood or bone marrow samples [4]. About 50% of patients are asymptomatic at the time of diagnosis and others have non-specific symptoms such as left upper quadrant pain, fullness, fatigue, malaise and night sweats. Bleeding is likely to occur when significant thrombocytopenia is present [2, 5].

Evolution of treatment of CML

Previously, recombinant interferon-alfa, low dose of cytarabine and allogeneic hematopoietic cell transplantation (HCT) were used as standard of care for CML [6]. HCT may be associated with a definite cure but complications and related mortality limits the utility [2]. Over the past 2 decades, patients with Ph+/BCR-ABL1 CML have been successfully treated by tyrosine kinase inhibitors (TKIs). TKIs have been effectively used against neoplasms associated with inappropriate activation of different tyrosine kinases and were associated with a better complete cytogenetic response (CCyR) compared to other treatments. In newly diagnosed CML cases who receive TKIs as standard treatment, the 5-year survival rates increased from 40–50% to 90% so that the lifespan of CML patients is nearly the same as general population [7, 8].

Different TKIs in CML

Imatinib, nilotinib, dasatinib, bosutinib, and ponatinib are TKIs approved by the US Food and Drug Administration (FDA) for treatment of patients with CML. These agents are different in efficacy and toxicity. Selection of a TKI depends on particular clinical feature and toxicity profile of each agent and also patient’s age, underlying diseases, and the goal of treatment [4, 9]. Imatinib 400 mg daily is the gold standard for treatment of CML. In patients who did not achieve clinical response or those did not tolerate treatment, higher doses (600 or 800 mg daily) is not recommended due to more adverse effects without improvement of clinical outcomes. Some second generation TKIs including nilotinib (300 mg twice daily) and dasatinib (100 mg once daily) may be used as the first line treatment [10, 11]. Efficace et al. [12] reported a better quality of life of chronic phase CML patients who were treated with dasatinib at the first line compared to imatinib. Bosutinib, another second generation TKI is approved for CML cases that are intolerant or resistant to prior first line therapies. Recent evidences from BFORE trial showed better clinical responses for bosutinib 400 mg once daily in comparison with imatinib 400 mg in newly diagnosed Ph+/BCR-ABL1 CML [13]. Ponatinib is the only TKI that was approved for CML patients with T315I mutation. It is also used as a second line treatment for cases who were resistant to imatinib, or experienced treatment failure/intolerance to other TKIs such as dasatinib, nilotinib or other second line agents [4].

TKIs-induced pulmonary toxicities

The incidence of pulmonary toxicities of TKIs is less than 1% [14]. The most reported toxicities were pulmonary artery hypertension (PAH), pleural effusion (PE), interstitial lung disease (ILD), pulmonary edema, chylothorax, cough, pneumonitis, bronchospasm and upper respiratory tract infection [15-21]. Most of these adverse reactions need discontinuing treatment and initiating a medical intervention [22]. Although PAH was not reported by using imatinib or nilotinib and rarely reported with lapatinib, ponatinib, and bosutinib, it is a known complication of dasatinib [23-27]. PE mostly occurres following treatment with dasatinib and bosutinib which could alter the patient’s compliance to the therapy. TKIs associated ILD is less likely to happen in which different histological markings lead to various clinical presentations [28]. In the following sections, we will focus on dasatinib-induced PE and PAH as two major pulmonary toxicities and their management will be discussed.

METHODS

We searched scientific databases for indexed studies on PubMed and Google-scholar based on the terms: “dasatinib”, “chronic myeloid leukemia”, “tyrosine kinase inhibitors”, “pulmonary arterial hypertension”, “pleural effusion”, and “pulmonary toxicity”. The Boolean operators (AND/OR) were also used to combine search terms. All case reports, case series, clinical trials, and relevant review articles were selected without limitation of the year of publication. Studies in languages other than English and those with only abstracts available were excluded.

DASATINIB

Efficacy in CML

Dasatinib, an oral potent second generation TKI, was approved in 2010 by FDA for management of newly diagnosed CML patients who are in chronic phase (100 mg once daily), and any phases of disease that is resistant or intolerant to previous treatment (70 mg twice daily) [29]. It is also used with 70 mg twice daily regimen in Ph+ acute lymphoblastic leukemia (ALL) [30-32]. Dasatinib inhibits BCR-ABL, SRC (v-src sarcoma viral oncogene homolog) family kinases (including SRC, LCK ,LYN, FYN, YES, HCK, FGR, BLK, YRK), receptor kinases (c-KIT, PDGFRβ, DDR 1 and 2, c-FMS, ephrin receptors), and TEC family kinases (TEC and BTK) [20, 30]. Dasatinib with its thiazole-carboxamide structure binds to the both active and inactive conformations of BCR-ABL1 while imatinib only inhibits inactive form [33]. It was efficacious on 18 out of 19 imatinib-resistant BCR-ABL mutations with the exception of T315I mutation [33, 34]. Results obtained from numerous prior studies demonstrated that dasatinib is superior to imatinib in terms of clinical outcomes including hematologic and cytogenetic responses with more potent activity against BCR-ABL1 (325 to 350 folds) [29, 31]. Various investigations have shown clinical efficacy of dasatinib over imatinib in both resistant and intolerant patients and also in newly diagnosed CML cases [29]. DASISION study was performed on treatment-naïve chronic phase CML patients to compare imatinib and dasatinib at the dose of 400 and 100 mg once daily, respectively. Analysis of long term results showed that dasatinib was associated with a faster and profound molecular response (MR), major molecular response and CCyR. Progression-free survival (PFS) and overall survival (OS) were high in both groups however patients in dasatinib group achieved an earlier response with a fewer CML-related death [35]. Another trial evaluated efficacy of different doses of dasatinib in imatinib-resistant or intolerant patients. The results showed that 100 mg daily dosing was associated with a better tolerability. A faster treatment response and also improvement in long term clinical benefits was reported with dasatinib [8].

Dasatinib adverse effects

Despite a dramatic improvement of survival of CML patients following approval of TKIs, various early and late adverse effects including gastrointestinal, cardiovascular, endocrine, hematologic and pulmonary toxicities were reported [36-39]. Gastrointestinal adverse effects include nausea and vomiting, diarrhea, abdominal pain, hemorrhagic colonic ulcers, acute hepatitis, anorexia, dyspepsia, and gastrointestinal bleeding as a result of platelet dysfunction. The mucosal inflammation including mucositis/stomatitis, constipation, acute pancreatitis, abdominal distension and colitis were seen in less than 10% of the cases. Endocrine disorders were gynecomastia, irregular menses, hypoglycemia, hyperglycemia and increased triglyceride and cholesterol levels [30, 32, 38, 40-42]. The most common cardiovascular effects were fluid retention, pericardial effusion, and to a lesser extent, cardiac dysfunction including cardiomegaly, angina, congestive heart failure and cardiac dysrhythmia including tachycardia and QTc prolongation [43-46]. Anemia, thrombocytopenia and neutropenia were reported with dasatinib which are most observed in Ph+ ALL patients and advanced phase CML patients compared to chronic phase. Thrombo-cytopenia is more clinically substantial and may result in central nervous system hemorrhage and gastrointestinal bleeding so that it is recommended to administrate dasatinib with caution in those receiving anticoagulation or antiplatelet agents [38, 46].
Dasatinib-induced pleural effusion: Pleural Effusion (PE) is a lymphocyte-predominant exudate, which has been observed with all BCR-ABL1 TKIs, but dasatinib has the most frequency (up to 35%) [14, 16, 47]. According to the Quintás-Cardama et al. [47] about 50% of dasatinib-induced PE cases were in accelerated phase of leukemia. Autoimmune inhibition of the PDGFR β which causes fluid retention has been suggested as involved mechanism of dasatinib-induced PE [48]. The occurrence of PE is one important cause of treatment withdrawal [49, 50]. The phase 3 of final DASISION trial has shown that the incidence of PE following use of TKIs were more common with dasatinib (28%) versus imatinib (0.8%) [35]. More dasatinib-induced PE occurred at the 5 years study results (29%) compared to the first year (10%). Most PE cases were in grade 1 (asymptomatic) or 2 (symptomatic; intervention such as diuretics or ≤2 therapeutic thoracenteses indicated) [51]. The incidence of PE was not associated with a negative effect on achieving clinical CCyR [35, 52]. Predisposing factors for PE were twice-daily dasatinib regimen, the initial daily dose of dasatinib (140 mg vs. 100 mg), other pulmonary diseases, the age of patient (60% in patients age ≥65 yr vs. 25% in patients younger than 65 yr), skin rash, hypercholesterolemia, as well as presence of hypertension, and a history of cardiac or autoimmune diseases. Based on the higher incidence of PE with twice-daily dosing of dasatinib, once-daily dosing regimen is now recommended for treatment of CML and ALL [16]. Univariate analysis of association between disease phase and development of PE revealed that treatment with dasatinib in accelerated phase and blast crisis is a risk factor for developing PE and patients whom treated particularly with higher doses of dasatinib should be accurately monitored for PE sign and symptoms [47]. Several studies reported that hypertension is a major comorbidity in patients with PE [35, 47, 49, 53, 54]. The animal model of dasatinib-induced PE indicated that in a dose-dependent manner, dasatinib could lead to altered pulmonary endothelial permeability which was reversible by decreasing dose or holding treatment and switching into other TKI. It was proposed that changes in intercellular junctions along with production of stress fibers in cytoplasm and reactive oxygen species (ROS) involve in the development of dasatinib-induced PE [54, 55].
Dasatinib-induced chylothorax is a rare pulmonary adverse effect that is a subgroup of PE and defined as triglycerides and cholesterol concentrations of pleural fluid more than 110 mg dL-1 (1.24 mmol L-1) and less than 200 mg dL-1 (5.18 mmol L-1), respectively [56]. Chylothorax results from obstruction or disruption of thoracic duct which leads to leakage of chyle into pleural space [19]. Despite aforementioned explanations, the exact molecular mechanism of PE and chylothorax has not been elucidated and needs further investigation [54, 57].
Dasatinib-induced pulmonary arterial hypertension: Pulmonary Arterial Hypertension (PAH) is one of the most severe pulmonary toxicities of TKIs and was mostly reported with dasatinib [14, 58]. PAH is a rare complication (0.45%) which is defined as increased mean pulmonary arterial pressure (mPAP) >25 mmHg at rest or >30 mmHg by exercising in the absence of elevated pulmonary capillary wedge pressure (PCWP) and pulmonary vascular resistance (PVR) >3 woods units that leads to right ventricular and progressively left ventricular failure [59]. In the presence of dyspnea, atypical chest pain, fatigue or unexplained syncope, Chest X-Ray (CXR) or trans-thoracic echocardiography (TTE) should be used and if PAH was proposed, right heart catheterization (RHC) should be performed to confirm the diagnosis [22]. On the basis of RHC results, PAH is determined as elevated right ventricular systolic pressure (RVSP) and/or pulmonary arterial systolic pressure above 40 mmHg. In addition, Toya et al. [60] conducted a study on 60 dasatinib treated cases and investigated whether which of the following items is more reliable for early predicting PAH: 1) recent electrocardiographic changes indicating right ventricular pressure overload; 2) estimated systolic pulmonary arterial pressure >40 mmHg measured by Doppler echocardiography; 3) computed tomography (CT)-measured pulmonary artery to aorta diameter (PaD/AoD) ratio >1; and 4) mean pulmonary arterial pressure >25 mmHg and pulmonary artery wedge pressure <15 mmHg measured by right heart catheterization. Although an increase in PaD/AoD ratio measured by CT imaging occurred in all cases, it was found that a significantly higher PaD/AoD ratio (>1) at baseline was seen in those developed PAH and it could be used as an early predictor of dasatinib-induced PAH. PAH happens on prolonged treatment with dasatinib (19–52 mo), confirming the chronicity nature of the involved pathological mechanism. Dasatinib-induced PAH predominantly occurs in women and is often concomitant with previous or present PE [15]. PAH in a CML patient may be drug-induced (group 1) or related to CML pathophysiology [15, 61-63]. It has been demonstrated that treatment with dasatinib causes a dose-dependent increase in production of mitochondrial ROS; resulting to endothelial apoptosis, pulmonary endothelial dysfunction and pulmonary hypertension. Another proposed mechanism is related to SRC family kinases and platelet-derived growth factor (PDGF) pathway [54, 62, 64]. SRC family kinases have a role in smooth muscle cells reproduction and also reducing pulmonary artery tone while their inhibition result in apoptosis and raised vascular resistance. Some recent studies indicated that pathways other than SRC may also play a role in endothelial dysfunction, which leads to dasatinib-induced PAH. Animal studies showed that the levels of soluble ICAM-1, soluble VCAM-1, and soluble E-selectin, markers of endothelial dysfunction, rises with dasatinib leading to less hypoxic vasoconstriction and subsequently impaired endoplasmic reticulum function [65]. There is no specific biomarker for PAH, but brain natriuretic peptide (BNP) and N-terminal pro-brain natriuretic peptide (NT-proBNP) have been used in clinical practice to evaluate the patient’s condition before and after the treatment [66-68]. Evaluation of the 6 minute walk distance (6-MWD) and world health organization (WHO) functional class is also useful in predicting prognosis of PAH treatment [59]. In a descriptive study of PAH cases in the French pulmonary hypertension registry from November 2006 to September 30, 2010, nine patients of dasatinib-induced PAH were reported. None of them had a chronic respiratory disease, family history of PAH or history of medications with the risk of PAH. Discontinuation of dasatinib led to improvement in clinical status of all patients except 3 who required further pharmacotherapy [15]. Although PAH is clinically reversible, the hemodynamic of patients may not completely improve after discontinuation of therapy [64].

MANAGEMENT

Since the widespread use of TKIs has made a tremendous change in the treatment of CML, the complications associated with these medications need to be identified and managed appropriately.

Pleural effusion

As noted above, treatment of CML with dasatinib was associated with a high prevalence and recurrence rate of PE. In a multivariate analysis, the most significant risk factor for incidence of PE was the patient’s age [69]. Dasatinib-induced PE has a clinically ameliorative nature in most cases. Dose interruption, dose reduction and drug therapy have been suggested for PE management [50, 54]. Based on radiographic features, patients with class 1 PE do not need any intervention. In patients who are categorized in class 2 or more and are asymptomatic, treatment should be interrupted and diuretics may be started in the presence of fluid retention. Therapy of CML should be resumed after resolution of effusion. Dose should be reduced in the case of further episodes. In symptomatic patients with PE≥class 2 or asymptomatic patients with PE≥class 3, dasatinib should be discontinued and corticosteroids (prednisone 40 mg daily for four days) should be initiated. Therapeutic thoracentesis should also be performed and the pleural fluid should be investigated to rule out other effusion causes. Dasatinib could be reintroduced in the case of effusion resolution. In symptomatic patients with PE≥class 2 or asymptomatic patients with PE≥class 3, dasatinib should be discontinued with recurrent PE [16].
Another approach for treatment is based on a different classification of PE severity. Cortes et al. [55] defined PE as following: “Small effusion” (volume of effusion <500 mL with a blunting view of costophrenic angle), “medium effusion” (with opacity above costophrenic angle) and “large effusion" (effusions more than 30 to 50% of hemithorax). Small effusion can be either symptomatic or asymptomatic. In patients with small asymptomatic PE, follow up of symptoms should be performed periodically with CXR monitoring every 3 months in the first year followed by every 6 months in the second year. For symptomatic patients, CXR should be repeated more frequently. Reducing the dose may be considered according to the level of therapeutic response in the chronic phase. In symptomatic PE, management includes dose reduction according to clinical response accompanied with a CXR after one month. If the size of PE was stable, the CXR monitoring should be repeated as mentioned above. In the case of persistent or worsening symptoms, its management is similar to medium/large effusion as will be noted. Medium/large effusions can be a result of worsening small symptomatic PE or diagnosed at presentation. For the first episode, treatment should be interrupted immediately until the effusion disappears and re-administered with lower dose based on the response of patient in the chronic phase. Prompt therapeutic thoracentesis is necessary for the first diagnosed medium/large PE followed by CXR every 2 to 4 weeks to evaluate volume of effusion. If more than 2 thoracenteses are needed, discontinuing of treatment is recommended. If the size of effusion did not change after thoracentesis, dose interruption and treatment with a lower dose of TKI based on response in the chronic phase is recommended (Fig. 1) [55].
Based on radical scavenging property, N-acetylcysteine (NAC) was effective in preventing increased pulmonary endothelial permeability which is one of the underlying causes of PE [54].

Pulmonary arterial hypertension

Pulmonary arterial hypertension (PAH) is a life threatening complication of long-term therapy with dasatinib, especially in the presence of PE. PAH may lead to right ventricular failure if left untreated [70, 71]. Reports represent low mortality rate due to dasatinib-induced PAH. Early diagnosis of PAH and cessation treatment with dasatinib are strongly recommended [59]. Discontinuation of dasatinib leads to notable symptomatic improvement, however this may not be associated with a complete hemodynamic recovery [64, 72]. Phosphodiesterase type-5 inhibitors, prostacyclin derivatives, and endothelin receptor antagonists (ERAs) are FDA approved pharmacological classes used for treatment of PAH. Riociguat, an oral soluble guanylate cyclase stimulator, is also another choice for management of PAH. A prostacyclin receptor agonist, selexipag has been approved by the FDA for PAH in 2015 [73]. Different FDA approved pharmacologic drugs, routes of administration and doses have been presented in Table 1. Several reports have been published according to the management of dasatinib-induced PAH. Clinical characteristics of patients, the intervention and outcome of therapy have been presented in Table 2.
Phosphodiesterase-5 inhibitors: Phosphodiesterase-5 (PDE-5) is the dominant isotype of PDE in the pulmonary vascular smooth cell muscles which is upregulated in PAH. It metabolizes cyclic guanosine monophosphate; hence PDE-5 inhibitors could induce nitric oxide-mediated vasodilation and possibly have some anti-proliferative effects [74, 75]. Sildenafil, tadalafil, and vardenafil have been studied in PAH and only sildenafil and tadalafil which are different in chemical structure have been approved by FDA for treatment of PAH [76, 77]. Due to the longer half-life of tadalafil (17.5 hr) as compared to that of sildenafil (∼4 hr), it is prescribed once daily whereas the other is taken 3 times per day [78]. They are similar in adverse effects profile and both tadalafil and sildenafil were associated with beneficial effects in exercise tolerability, hemodynamic parameters and clinical status of dasatinib-induced PAH [79].
WHO functional class, 6-MWD, mPAP, and clinical worsening were assessed in 278 PAH patients who received either placebo or sildenafil (20 mg, 40 mg, or 80 mg) orally 3 times daily for 12 weeks. A notable improvement in all mentioned values was achieved after all doses. Since complete inhibition of PDE-5 at the dose of 20 mg 3 times was achieved, dose escalation to get much more response is not reasonable [75]. The efficacy of sildenafil in dasatinib-induced PAH has been evaluated in numerous case reports [80-84]. Groeneveldt and coworkers reported a case with mPAP of 55 mmHg and NYHA functional class 4 who had no improvement in NYHA functional class after being treated with sildenafil. Actually, dasatinib was not discontinued in spite of emphasis on stopping treatment immediately after the appearance of PAH [59, 85]. Sildenafil was also evaluated in combination with bosentan (20 mg TDS and 62.5 mg BD, respectively) in a patient with mPAP of 37 mmHg, WHO functional class 2 and BNP 685 pg mL-1. All variables improved after 6 months of treatment [86]. In another case, right ventricle systolic pressure (RVSP) was reduced from 71 mmHg to 55 mmHg after treatment with 25 mg once daily sildenafil. Re-challenging of dasatinib after reduction of RVSP was associated with a faster incidence of PAH appearance [61].
In a large trial, tadalafil, another PDE-5 inhibitor, was investigated in doses of 2.5 mg, 10 mg, 20 mg and 40 mg once daily for management of PAH in 405 patients. Borg dyspnea score (BDS), 6-MWD, clinical worsening, health-related quality of life and WHO functional class were assessed. Only the 40 mg/day dose showed statistically significant improvement in all of measurements except WHO functional class and BDS [87]. Until today there is no study to evaluate tadalafil monotherapy in dasatinib-induced PAH, as it was used in combination with other drugs. An abstract published in January 2020 in European Heart Journal Cardiovascular Imaging showed that combination of tadalafil and ambrisentan is effective in improvement of systolic PAP and secondary myocardium changes caused by dasatinib [88]. Two other different dosage regimens of tadalafil and ambrisentan combination were used: “tadalafil (40 mg daily)+ambrisentan (10 mg daily)” and “tadalafil (20 mg daily)+ambrisentan (5 mg daily)”. Both revealed improvement in pulmonary symptoms, mPAP, 6-MWD, BNP level and WHO functional class [62, 64].
Endothelin receptor-1 antagonists (ERAs): Bosentan, ambrisentan and macitentan are ERAs approved by FDA for management of PAH. Bosentan, the oldest member of ERAs is a non-selective competitive antagonist of endothelin receptor-1 (ET-1) that irreversibly blocks both ET-1A and ET-1B [89, 90]. The efficacy of bosentan in PAH was evaluated in BREATHE-1 study. Patients were treated with 62.5 mg BD bosentan for 4 weeks and then randomly assigned to receive 125 mg or 250 mg twice daily for a minimum of additional 12 weeks. Amelioration of exercise capacity as primary outcome of the trial was seen in both bosentan-treated groups (P<0.001). Changes in the BDS, WHO functional class, and the time to clinical worsening were considered as secondary endpoints. Reduction in BDS was greater in patients received 250 mg twice daily in comparison with 125 mg twice daily. In total, WHO functional class decreased 42% in patients received bosentan versus 30% in patients received placebo. Time to clinical worsening was longer in patients in bosentan group compared to patients in placebo group after 16 weeks. Hepatic dysfunction occurred in a dose dependent manner and was more frequent with 250 mg BD dosing. Surprisingly, the changes in mPAP were not clinically significant notwithstanding in study group received high dose of bosentan (250 mg BD) (88±13 mmHg at baseline versus 85±11 mmHg at the end of trial) [91]. Reversible elevation in aminotransferases, anemia, headache and edema were the complications associated with bosentan [92, 93]. The only published paper about dasatinib-induced PAH treated with bosentan was a patient with acute lymphoblastic leukemia (ALL). Titration of bosentan to a dose of 125 mg twice daily led to significant decrease in systolic pulmonary artery pressure (SPAP) and pro-BNP level. NYHA functional class and also 6-MWD significantly improved during the intervention [94].
Among above mentioned three agents, ambrisentan is a selective blocker of ET-1A which is responsible for smooth muscle cells vasoconstriction. The incidence of liver impairment and drug interactions of ambrisentan was lower but it was associated with a more frequency of peripheral edema [95-97]. Data demonstrated that selectivity on ETR blockage was not an important factor in choosing an agent for PAH management. The role of ambrisentan in combination with tadalafil in dasatinib-induced PAH was evaluated just in case reports as mentioned previously [98]. Along with discontinuation of dasatinib, ambrisentan in combination with sildenafil and treprostinil was associated with improvement in mPAP, 6-MWD and NYHA functional class. However, an unexpected progression of PAH occurred after 3 years which was not controlled by intensive anti PAH therapy and resulted in need for lung transplantation. It is notable that the CML therapy may be resumed with nilotinib in patients with PAH following dasatinib use [99].
Macitentan is a novel non-selective ET-1 antagonist with an active metabolite with a longer half-life compared to the parent drug. Macitentan and its active metabolite have a higher tendency to tissue and bind more potently to ET receptors compared to the other ET-1As [100]. It has a good safety profile with well-tolerated adverse events include nausea, vomiting and headache and less liver toxicity compared to bosentan and ambrisentan [101]. This highly potent ERAs was studied in SERAPHIN trial with the dosage regimens of 3 mg and 10 mg once daily versus placebo in 742 PAH cases (not dasatinib-induced PAH). Both 3 mg (P=0.01) and 10 mg (P<0.0001) once daily dosing reduced the risk of morbidity/mortality by 30% and 45%, respectively. NYHA functional class and 6-MWD changes from baseline were the secondary endpoints of study. Overall, macitentan was well tolerated and adverse effects including nasopharyngitis, headache and anemia were similar in all groups [102]. It also reduced PAH-related hospitalization and chronic thromboembolic pulmonary hypertension [103]. In a case of Dasatinib-induced PAH with concurrent scleroderma, macitentan was used along with tadalafil and selexipag. Rapid improvement of mPAP, 6-MWD and NYHA functional class were reported [104].
Sitaxentan, a selective ERA, was eliminated from the market because of its lethal liver toxicity [105-107].
Epoprostenol and prostaglandin I2 (PGI2) derivatives: Epoprostenol as a synthetic derivative of PGI2 received FDA approval in 1995. PGI2 acts as a direct vasodilator and also a cytoprotective agent which inhibits platelet aggregation [108-110]. Epoprostenol has beneficial effects on PAH symptoms, disease progression, 6-MWD and survival [111-115]. A case of dasatinib-induced PAH was treated successfully with epoprostenol along with discontinuation of dasatinib [116]. According to epoprostenol instability in plasma, continuous intravenous infusion (IV) is the preferred route of administration, though it is linked to catheter-related thrombosis and infection [114, 117, 118]. Other adverse effects were ascites, thrombocytopenia, flushing, headache, nausea, loose stool, jaw discomfort and musculoskeletal pain [110, 119].
Treprostinil is another prostanoid with longer half-life used in treatment of PAH. It was associated with improvement in quality of life, exercise capacity, functional class, pulmonary hemodynamics, and survival of patients [120-123]. Treprostinil can be used in oral, inhaled, subcutaneous or IV routes which the 2 latter are assumed bioequivalent at steady state in the dose of 10 ng kg-1min-1. It is also used as SC infusion. Local pain following infusion may occur and could be decreased by titrating of dose during 6 months [124, 125]. Transition from IV epoprostenol to IV or SC treprostinil is rational when patient is intolerant to epoprostenol or in the case of worsening of clinical status [126-128]. Inhaled treprostinil in patients with severe pulmonary hypertension revealed a significant sustained impact on pulmonary vascular resistance compared to the same doses of inhaled iloprost with a better tolerability profile [129]. According to a double-blind, randomized, placebo-controlled trial, continuous SC infusion of treprostinil enhances exercise capacity regardless of the PAH etiology. Considering this dose-related effect, treprostinil could be an appropriate agent for management of dasatinib-induced PAH [130].
Iloprost, an analog of PGI2 has a short half-life of 20–25 minutes and was used as inhalation or IV forms with frequent doses (e.g., 6–9 times daily) [131]. It can improve 6-MWD, Mahler dyspnea index, quality of life and NYHA functional class in PAH by inhaled formulation [132]. Despite its inhalation form, IV iloprost did not receive FDA approval for PAH. Both iloprost and treprostinil inhalation formulations lead to cough [133].
Beraprost is an oral rapid onset analog of PGI2 that improves 6-MWD, disease progression and WHO functional class. Considering WHO functional class, the beneficial effects is limited to 6 months [134]. Beraprost and Iloprost have not yet studied for management of dasatinib-induced PAH, but they could be acceptable drugs since both have proven efficacy in ameliorating the PAH with other etiologies.
Selexipag is another oral prostacyclin IP2-receptor (IP2r) agonist with a non-prostanoid structure. It has a vasodilator effect on large and small pulmonary arterial branches [135-137]. Selexipag has the highest affinity for IP2r with similar side effect profile of other IP2r agonists. Headache is the most common adverse effect along with jaw pain, nausea and diarrhea which are often observed with rapid dose-titration and are reduced over time [138]. Selexipag showed a significant improvement in the primary composite endpoint of death, complications related to PAH, pulmonary vascular resistance and 6-MWD in GRIPHON trial [136]. As mentioned previously, selexipag has been studied in dasatinib-induced PAH in combination with macitentan and tadalafil resulted in rapid improvement of mPAP, 6-MWD and NYHA functional class [104].
Calcium channel blockers (CCBs): CCBs reduces the influx of calcium in smooth muscle cells leading to systemic peripheral arterial dilation. Therapeutic effects of CCBs will be obtained when used at high doses for a long time [139-143]. Among long acting nifedipine, diltiazem and amlodipine, diltiazem is preferred when the heart rate is above 80 beats min-1 [144, 145]. Verapamil is not recommended due to its notable negative inotropic effect [146]. Although CCBs have been noted nearly in all PAH treatment guidelines, in fact a very few numbers of patients with PAH including idiopathic-PAH patients, genetically associated PAH, or anorexigen-induced PAH will benefit from using high doses and long term CCB therapy [147]. It doesn’t seem that CCBs are effective in dasatinib-induced PAH [148].

CONCLUSION

Pulmonary complications of TKIs need to be diagnosed and managed promptly. Dasatinib was associated with a higher prevalence and recurrence rate of PE and PAH among TKIs. In symptomatic patients with mild PE, dasatinib should be interrupted and in the case of fluid retention, diuretics should be initiated. Therapy of CML should be resumed after resolution of effusion. In symptomatic patients with PE ≥class 2 or asymptomatic patients with PE ≥class 3, dasatinib should be discontinued and corticosteroids (prednisone 40 mg daily for four days) should be initiated along with therapeutic thoracentesis. PAH is a life threatening complication of long-term therapy with dasatinib. Phosphodiesterase type-5 inhibitors (e.g., sildenafil and tadalafil) alone or in combination with endothelin receptor-1 antagonists (e.g., bosentan and macitentan) and also synthetic derivatives of PGI2 or non-prostanoid prostacyclin-receptor agonist (e.g., selexipag) were successfully used in the management of dasatinib-induced PAH. Current recommendations regarding the management of pulmonary toxicities of TKIs including dasatinib are based on published case reports and evaluating the safety and efficacy of different available pharmacotherapies require conducting multi-center randomized controlled trials.

Notes

Authors’ Disclosures of Potential Conflicts of Interest

No potential conflicts of interest relevant to this article were reported.

REFERENCES

1. Kaiafa G, Kakaletsis N, Savopoulos C, et al. 2014; Simultaneous manifestation of pleural effusion and acute renal failure associated with dasatinib: a case report. J Clin Pharm Ther. 39:102–5. DOI: 10.1111/jcpt.12107. PMID: 24188312.
crossref
2. Jabbour E, Kantarjian H. 2018; Chronic myeloid leukemia: 2018 update on diagnosis, therapy and monitoring. Am J Hematol. 93:442–59. DOI: 10.1002/ajh.25011. PMID: 29411417.
crossref
3. Radich JP, Deininger M, Abboud CN, et al. 2018; Chronic myeloid leukemia, version 1.2019, NCCN clinical practice guidelines in oncology. J Natl Compr Canc Netw. 16:1108–35. DOI: 10.6004/jnccn.2018.0071. PMID: 30181422.
4. Hochhaus A, Saussele S, Rosti G, et al. 2017; Chronic myeloid leukaemia: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol. 28(Suppl 4):iv41–51. DOI: 10.1093/annonc/mdx219. PMID: 28881915.
crossref
5. Thompson PA, Kantarjian HM, Cortes JE. 2015; Diagnosis and treatment of chronic myeloid leukemia in 2015. Mayo Clin Proc. 90:1440–54. DOI: 10.1016/j.mayocp.2015.08.010. PMID: 26434969. PMCID: PMC5656269.
crossref
6. Larson RA. 2015; Is there a best TKI for chronic phase CML? Hematology Am Soc Hematol Educ Program. 2015:250–6. DOI: 10.1182/asheducation-2015.1.250. PMID: 26637730.
crossref
7. Moslehi JJ, Deininger M. 2015; Tyrosine kinase inhibitor-associated cardiovascular toxicity in chronic myeloid leukemia. J Clin Oncol. 33:4210–8. DOI: 10.1200/JCO.2015.62.4718. PMID: 26371140. PMCID: PMC4658454.
crossref
8. Shah NP, Rousselot P, Schiffer C, et al. 2016; Dasatinib in imatinib‐resistant or‐intolerant chronic‐phase, chronic myeloid leukemia patients: 7‐year follow‐up of study CA180‐034. Am J Hematol. 91:869–74. DOI: 10.1002/ajh.24423. PMID: 27192969. PMCID: PMC5094534.
9. Medeiros BC, Possick J, Fradley M. 2018; Cardiovascular, pulmonary, and metabolic toxicities complicating tyrosine kinase inhibitor therapy in chronic myeloid leukemia: strategies for monitoring, detecting, and managing. Blood Rev. 32:289–99. DOI: 10.1016/j.blre.2018.01.004. PMID: 29454474.
crossref
10. García-Gutiérrez V, Hernández-Boluda JC. 2019; Tyrosine kinase inhibitors available for chronic myeloid leukemia: efficacy and safety. Front Oncol. 9:603. DOI: 10.3389/fonc.2019.00603. PMID: 31334123. PMCID: PMC6617580.
crossref
11. Baccarani M, Deininger MW, Rosti G, et al. 2013; European LeukemiaNet recommendations for the management of chronic myeloid leukemia: 2013. Blood. 122:872–84. DOI: 10.1182/blood-2013-05-501569. PMID: 23803709. PMCID: PMC4915804.
12. Efficace F, Stagno F, Iurlo A, et al. 2020; Health-related quality of life of newly diagnosed chronic myeloid leukemia patients treated with first-line dasatinib versus imatinib therapy. Leukemia. 34:488–98. DOI: 10.1038/s41375-019-0563-0. PMID: 31477798.
crossref
13. Cortes JE, Gambacorti-Passerini C, Deininger MW, et al. 2018; Bosutinib versus imatinib for newly diagnosed chronic myeloid leukemia: results from the randomized BFORE trial. J Clin Oncol. 36:231–7. DOI: 10.1200/JCO.2017.74.7162. PMID: 29091516. PMCID: PMC5966023.
14. Caldemeyer L, Dugan M, Edwards J, Akard L. 2016; Long-term side effects of tyrosine kinase inhibitors in chronic myeloid leukemia. Curr Hematol Malig Rep. 11:71–9. DOI: 10.1007/s11899-016-0309-2. PMID: 26922746.
crossref
15. Montani D, Bergot E, Günther S, et al. 2012; Pulmonary arterial hypertension in patients treated by dasatinib. Circulation. 125:2128–37. DOI: 10.1161/CIRCULATIONAHA.111.079921. PMID: 22451584.
16. Brixey AG, Light RW. 2010; Pleural effusions due to dasatinib. Curr Opin Pulm Med. 16:351–6. DOI: 10.1097/MCP.0b013e328338c486. PMID: 20375898.
crossref
17. Jasielec JK, Larson RA. 2016; Dasatinib-related pulmonary toxicity mimicking an atypical infection. J Clin Oncol. 34:e46–8. DOI: 10.1200/JCO.2013.50.1981. PMID: 24958829.
crossref
18. Fazakas C, Nagaraj C, Zabini D, et al. 2018; Rho-kinase inhibition ameliorates dasatinib-induced endothelial dysfunction and pulmonary hypertension. Front Physiol. 9:537. DOI: 10.3389/fphys.2018.00537. PMID: 29867576. PMCID: PMC5962749.
crossref
19. Huang YM, Wang CH, Huang JS, et al. 2015; Dasatinib-related chylothorax. Turk J Haematol. 32:68–72. DOI: 10.4274/tjh.2012.0196. PMID: 25805678. PMCID: PMC4439910.
crossref
20. Bergeron A, Réa D, Levy V, et al. 2007; Lung abnormalities after dasatinib treatment for chronic myeloid leukemia: a case series. Am J Respir Crit Care Med. 176:814–8. DOI: 10.1164/rccm.200705-715CR. PMID: 17600277.
21. Al-Ameri AM, Kantarjian H, Burton E, et al. 2009; Low risk of infectious events in patients (Pts) with chronic myeloid leukemia (CML) in chronic phase (CP) treated with dasatinib. Blood (ASH Annual Meeting Abstracts). 114(Suppl):3291. DOI: 10.1182/blood.V114.22.3291.3291.
22. Özgür Yurttaş N, Eşkazan AE. 2018; Dasatinib-induced pulmonary arterial hypertension. Br J Clin Pharmacol. 84:835–45. DOI: 10.1111/bcp.13508. PMID: 29334406. PMCID: PMC5903230.
crossref
23. Quilot FM, Georges M, Favrolt N, et al. 2016; Pulmonary hypertension associated with ponatinib therapy. Eur Respir J. 47:676–9. DOI: 10.1183/13993003.01110-2015. PMID: 26743481.
crossref
24. Riou M, Seferian A, Savale L, et al. 2016; Deterioration of pulmonary hypertension and pleural effusion with bosutinib following dasatinib lung toxicity. Eur Respir J. 48:1517–9. DOI: 10.1183/13993003.01410-2016. PMID: 27799395.
crossref
25. Hickey PM, Thompson AA, Charalampopoulos A, et al. 2016; Bosutinib therapy resulting in severe deterioration of pre-existing pulmonary arterial hypertension. Eur Respir J. 48:1514–6. DOI: 10.1183/13993003.01004-2016. PMID: 27660511.
crossref
26. Alkhatib Y, Albashaireh D, Al-Aqtash T, Awdish R. 2016; The role of tyrosine kinase inhibitor "Lapatinib" in pulmonary hypertension. Pulm Pharmacol Ther. 37:81–4. DOI: 10.1016/j.pupt.2016.03.002. PMID: 26965087.
crossref
27. Weatherald J, Chaumais MC, Montani D. 2017; Pulmonary arterial hypertension induced by tyrosine kinase inhibitors. Curr Opin Pulm Med. 23:392–7. DOI: 10.1097/MCP.0000000000000412. PMID: 28639957.
crossref
28. Weatherald J, Bondeelle L, Chaumais MC, et al. 2020; Pulmonary complications of Bcr-Abl tyrosine kinase inhibitors. Eur Respir J. 56:2000279. DOI: 10.1183/13993003.00279-2020. PMID: 32527740.
crossref
29. Chen R, Chen B. 2015; The role of dasatinib in the management of chronic myeloid leukemia. Drug Des Devel Ther. 9:773–9. DOI: 10.2147/DDDT.S80207. PMID: 25709401. PMCID: PMC4330036.
30. Lindauer M, Hochhaus A. 2014; Dasatinib. In: Martens UM, ed. Small molecules in oncology. Heidelberg, Germany:. Springer,. 27–65. DOI: 10.1007/978-3-642-54490-3_2. PMID: 24756784.
31. Rosti G, Castagnetti F, Gugliotta G, Baccarani M. 2017; Tyrosine kinase inhibitors in chronic myeloid leukaemia: which, when, for whom? Nat Rev Clin Oncol. 14:141–54. DOI: 10.1038/nrclinonc.2016.139. PMID: 27752053.
crossref
32. Lindauer M, Hochhaus A. 2018; Dasatinib. In: Martens UM, ed. Small molecules in hematology. Heidelberg, Germany:. Springer,. 29–68. DOI: 10.1007/978-3-319-91439-8_2. PMID: 30069624.
33. Mughal TI, Radich JP, Deininger MW, et al. 2016; Chronic myeloid leukemia: reminiscences and dreams. Haematologica. 101:541–58. DOI: 10.3324/haematol.2015.139337. PMID: 27132280. PMCID: PMC5004358.
crossref
34. Bradeen HA, Eide CA, O'Hare T, et al. 2006; Comparison of imatinib mesylate, dasatinib (BMS-354825), and nilotinib (AMN107) in an N-ethyl-N-nitrosourea (ENU)-based mutagenesis screen: high efficacy of drug combinations. Blood. 108:2332–8. DOI: 10.1182/blood-2006-02-004580. PMID: 16772610. PMCID: PMC1895563.
crossref
35. Cortes JE, Saglio G, Kantarjian HM, et al. 2016; Final 5-year study results of DASISION: the dasatinib versus imatinib study in treatment-naïve chronic myeloid leukemia patients trial. J Clin Oncol. 34:2333–40. DOI: 10.1200/JCO.2015.64.8899. PMID: 27217448. PMCID: PMC5118045.
crossref
36. Caocci G, Atzeni S, Orrù N, et al. 2008; Gynecomastia in a male after dasatinib treatment for chronic myeloid leukemia. Leukemia. 22:2127–8. DOI: 10.1038/leu.2008.106. PMID: 18463676.
crossref
37. Lundholm M, Charnogursky G. 2019; A case of dasatinib-induced hypoglycemia. Endocrine Practice. 25:85. DOI: 10.1016/S1530-891X(20)46580-2.
38. Aguilera DG, Tsimberidou AM. 2009; Dasatinib in chronic myeloid leukemia: a review. Ther Clin Risk Manag. 5:281–9. DOI: 10.2147/TCRM.S3425. PMID: 19536317. PMCID: PMC2697539.
39. Yu L, Liu J, Huang X, Jiang Q. 2019; Adverse effects of dasatinib on glucose-lipid metabolism in patients with chronic myeloid leukaemia in the chronic phase. Sci Rep. 9:17601. DOI: 10.1038/s41598-019-54033-0. PMID: 31772301. PMCID: PMC6879732.
crossref
40. Kostos L, Burbury K, Srivastava G, Prince HM. 2015; Gastrointestinal bleeding in a chronic myeloid leukaemia patient precipitated by dasatinib-induced platelet dysfunction: case report. Platelets. 26:809–11. DOI: 10.3109/09537104.2015.1049138. PMID: 26029798.
crossref
41. Ono Y, Mori T, Kato J, et al. 2010; Hemorrhagic colonic ulcers caused by dasatinib for chronic myelogenous leukemia. Int J Hematol. 92:556–8. DOI: 10.1007/s12185-010-0677-7. PMID: 20824400.
crossref
42. Bonvin A, Mesnil A, Nicolini FE, et al. 2008; Dasatinib-induced acute hepatitis. Leuk Lymphoma. 49:1630–2. DOI: 10.1080/10428190802136384. PMID: 18608866.
crossref
43. Dasanu CA, Padmanabhan P, Clark BA 3rd, Do C. 2012; Cardio-vascular toxicity associated with small molecule tyrosine kinase inhibitors currently in clinical use. Expert Opin Drug Saf. 11:445–57. DOI: 10.1517/14740338.2012.672971. PMID: 22469002.
crossref
44. Kim DW, Saussele S, Williams LA, et al. 2018; Outcomes of switching to dasatinib after imatinib-related low-grade adverse events in patients with chronic myeloid leukemia in chronic phase: the DASPERSE study. Ann Hematol. 97:1357–67. DOI: 10.1007/s00277-018-3295-8. PMID: 29556695. PMCID: PMC6018625.
crossref
45. 2021. Sprycel prescribing information. Bristol-Myers Squibb;New York, NY: at https://packageinserts.bms.com/pi/pi_sprycel.pdf. Accessed July 10, 2021.
46. Keating GM. 2017; Dasatinib: a review in chronic myeloid leukaemia and ph+ acute lymphoblastic leukaemia. Drugs. 77:85–96. DOI: 10.1007/s40265-016-0677-x. PMID: 28032244.
crossref
47. Quintás-Cardama A, Kantarjian H, O'brien S, et al. 2007; Pleural effusion in patients with chronic myelogenous leukemia treated with dasatinib after imatinib failure. J Clin Oncol. 25:3908–14. DOI: 10.1200/JCO.2007.12.0329. PMID: 17761974.
crossref
48. Shah NP, Kantarjian HM, Kim DW, et al. 2008; Intermittent target inhibition with dasatinib 100 mg once daily preserves efficacy and improves tolerability in imatinib-resistant and-intolerant chronic-phase chronic myeloid leukemia. J Clin Oncol. 26:3204–12. DOI: 10.1200/JCO.2007.14.9260. PMID: 18541900.
49. Iurlo A, Galimberti S, Abruzzese E, et al. 2018; Pleural effusion and molecular response in dasatinib-treated chronic myeloid leukemia patients in a real-life Italian multicenter series. Ann Hematol. 97:95–100. DOI: 10.1007/s00277-017-3144-1. PMID: 28971265.
crossref
50. Latagliata R, Breccia M, Fava C, et al. 2013; Incidence, risk factors and management of pleural effusions during dasatinib treatment in unselected elderly patients with chronic myelogenous leukaemia. Hematol Oncol. 31:103–9. DOI: 10.1002/hon.2020. PMID: 22815278.
crossref
51. 2009. Common terminology criteria for adverse events (CTCAE). Version 4.0. National Cancer Institute;Bethesda, MD:
52. Cortes JE, Saglio G, Baccarani M, et al. 2014; Final study results of the phase 3 dasatinib versus imatinib in newly diagnosed chronic myeloid leukemia in chronic phase (CML-CP) trial (DASISION, CA180-056). Blood (ASH Annual Meeting Abstracts). 124(Suppl):152. DOI: 10.1182/blood.V124.21.152.152.
crossref
53. Kantarjian H, Cortes J, Kim DW, et al. 2009; Phase 3 study of dasatinib 140 mg once daily versus 70 mg twice daily in patients with chronic myeloid leukemia in accelerated phase resistant or intolerant to imatinib: 15-month median follow-up. Blood. 113:6322–9. DOI: 10.1182/blood-2008-11-186817. PMID: 19369231. PMCID: PMC4916944.
crossref
54. Phan C, Jutant EM, Tu L, et al. 2018; Dasatinib increases endothelial permeability leading to pleural effusion. Eur Respir J. 51:1701096. DOI: 10.1183/13993003.01096-2017. PMID: 29348177.
crossref
55. Cortes JE, Jimenez CA, Mauro MJ, Geyer A, Pinilla-Ibarz J, Smith BD. 2017; Pleural effusion in dasatinib-treated patients with chronic myeloid leukemia in chronic phase: identification and management. Clin Lymphoma Myeloma Leuk. 17:78–82. DOI: 10.1016/j.clml.2016.09.012. PMID: 28082112.
crossref
56. Baloch ZQ, Abbas SA, Bhatti H, Braver Y, Ali SK. 2017; Dasatinib-induced chylothorax in chronic myeloid leukemia. Proc (Bayl Univ Med Cent). 30:71–3. DOI: 10.1080/08998280.2017.11929535. PMID: 28127140. PMCID: PMC5242121.
crossref
57. Ferreiro L, San-José E, Suárez-Antelo J, Valdés L. 2016; Dasatinib-induced pleural effusion: chylothorax, an option to consider. Ann Thorac Med. 11:289–93. DOI: 10.4103/1817-1737.191871. PMID: 27803756. PMCID: PMC5070439.
crossref
58. Rix U, Hantschel O, Dürnberger G, et al. 2007; Chemical proteomic profiles of the BCR-ABL inhibitors imatinib, nilotinib, and dasatinib reveal novel kinase and nonkinase targets. Blood. 110:4055–63. DOI: 10.1182/blood-2007-07-102061. PMID: 17720881.
crossref
59. El-Dabh A, Acharya D. 2019; EXPRESS: pulmonary hypertension with dasatinib and other tyrosine kinase inhibitors. Pulm Circ. 9:2045894019865704. DOI: 10.1177/2045894019865704. PMID: 31274047. PMCID: PMC6664660.
60. Toya T, Nagatomo Y, Kagami K, et al. 2019; Computed tomography-measured pulmonary artery to aorta ratio and EUTOS score for detecting dasatinib-induced pulmonary arterial hypertension. Int J Cardiovasc Imaging. 35:1435–42. DOI: 10.1007/s10554-019-01548-2. PMID: 30715668.
crossref
61. Hong JH, Lee SE, Choi SY, et al. 2015; Reversible pulmonary arterial hypertension associated with dasatinib for chronic myeloid leukemia. Cancer Res Treat. 47:937–42. DOI: 10.4143/crt.2013.155. PMID: 25648097. PMCID: PMC4614213.
crossref
62. Ibrahim U, Saqib A, Dhar V, Odaimi M. 2019; Dasatinib-induced pulmonary arterial hypertension - a rare late complication. J Oncol Pharm Pract. 25:727–30. DOI: 10.1177/1078155217753740. PMID: 29343154.
crossref
63. Simonneau G, Gatzoulis MA, Adatia I, et al. 2013; Updated clinical classification of pulmonary hypertension. J Am Coll Cardiol. 62(25 Suppl):D34–41. DOI: 10.1016/j.jacc.2013.10.029. PMID: 24355639.
crossref
64. Jose A, Rafei H, Ahari J. 2017; Combination targeted pulmonary hypertension therapy in the resolution of dasatinib-associated pulmonary arterial hypertension. Pulm Circ. 7:803–7. DOI: 10.1177/2045893217716659. PMID: 28644066. PMCID: PMC5703121.
crossref
65. Guignabert C, Phan C, Seferian A, et al. 2016; Dasatinib induces lung vascular toxicity and predisposes to pulmonary hypertension. J Clin Invest. 126:3207–18. DOI: 10.1172/JCI86249. PMID: 27482885. PMCID: PMC5004960.
crossref
66. Galiè N, Humbert M, Vachiery JL, et al. 2016; 2015 ESC/ERS guidelines for the diagnosis and treatment of pulmonary hypertension: the Joint Task Force for the Diagnosis and Treatment of Pulmonary Hypertension of the European Society of Cardiology (ESC) and the European Respiratory Society (ERS): endorsed by: Association for European Paediatric and Congenital Cardiology (AEPC), International Society for Heart and Lung Transplantation (ISHLT). Eur Heart J. 37:67–119. DOI: 10.1093/eurheartj/ehv317. PMID: 26320113.
67. Minami M, Arita T, Iwasaki H, et al. 2017; Comparative analysis of pulmonary hypertension in patients treated with imatinib, nilotinib and dasatinib. Br J Haematol. 177:578–87. DOI: 10.1111/bjh.14608. PMID: 28340283.
crossref
68. Warwick G, Thomas PS, Yates DH. 2008; Biomarkers in pulmonary hypertension. Eur Respir J. 32:503–12. DOI: 10.1183/09031936.00160307. PMID: 18669790.
crossref
69. Hughes TP, Laneuville P, Rousselot P, et al. 2019; Incidence, outcomes, and risk factors of pleural effusion in patients receiving dasatinib therapy for Philadelphia chromosome-positive leukemia. Haematologica. 104:93–101. DOI: 10.3324/haematol.2018.188987. PMID: 30093398. PMCID: PMC6312029.
crossref
70. Skride A, Sablinskis M, Sablinskis K, Lesina K, Lejnieks A, Lejniece S. 2017; Pulmonary arterial hypertension in a patient treated with dasatinib: a case report. J Med Case Rep. 11:362. DOI: 10.1186/s13256-017-1515-9. PMID: 29287600. PMCID: PMC5747081.
crossref
71. Buchelli Ramirez HL, Álvarez Álvarez CM, Rodríguez Reguero JJ, García Clemente MM, Casan Clarà P. 2014; Reversible pre-capillary pulmonary hypertension due to dasatinib. Respir Care. 59:e77–80. DOI: 10.4187/respcare.02692. PMID: 24149673.
crossref
72. Jabbour E, Kantarjian HM, Saglio G, et al. 2014; Early response with dasatinib or imatinib in chronic myeloid leukemia: 3-year follow-up from a randomized phase 3 trial (DASISION). Blood. 123:494–500. DOI: 10.1182/blood-2013-06-511592. PMID: 24311723. PMCID: PMC4190618.
crossref
73. Klinger JR, Elliott CG, Levine DJ, et al. 2019; Therapy for pulmonary arterial hypertension in adults: update of the CHEST guideline and expert panel report. Chest. 155:565–86. DOI: 10.1016/j.chest.2018.11.030. PMID: 30660783.
74. Jernigan NL, Resta TC. 2002; Chronic hypoxia attenuates cGMP-dependent pulmonary vasodilation. Am J Physiol Lung Cell Mol Physiol. 282:L1366–75. DOI: 10.1152/ajplung.00273.2001. PMID: 12003794.
75. Galiè N, Ghofrani HA, Torbicki A, et al. 2005; Sildenafil citrate therapy for pulmonary arterial hypertension. N Engl J Med. 353:2148–57. DOI: 10.1056/NEJMoa050010. PMID: 16291984.
crossref
76. Ghofrani HA, Voswinckel R, Reichenberger F, et al. 2004; Differences in hemodynamic and oxygenation responses to three different phosphodiesterase-5 inhibitors in patients with pulmonary arterial hypertension: a randomized prospective study. J Am Coll Cardiol. 44:1488–96. DOI: 10.1016/S0735-1097(04)01362-2. PMID: 15464333.
77. Montani D, Chaumais MC, Savale L, et al. 2009; Phosphodiesterase type 5 inhibitors in pulmonary arterial hypertension. Adv Ther. 26:813–25. DOI: 10.1007/s12325-009-0064-z. PMID: 19768639.
crossref
78. Wright PJ. 2006; Comparison of phosphodiesterase type 5 (PDE5) inhibitors. Int J Clin Pract. 60:967–75. DOI: 10.1111/j.1742-1241.2006.01049.x. PMID: 16780568.
crossref
79. Montani D, Chaumais MC, Guignabert C, et al. 2014; Targeted therapies in pulmonary arterial hypertension. Pharmacol Ther. 141:172–91. DOI: 10.1016/j.pharmthera.2013.10.002. PMID: 24134901.
crossref
80. Orlandi EM, Rocca B, Pazzano AS, Ghio S. 2012; Reversible pulmonary arterial hypertension likely related to long-term, low-dose dasatinib treatment for chronic myeloid leukaemia. Leuk Res. 36:e4–6. DOI: 10.1016/j.leukres.2011.08.007. PMID: 21890201.
crossref
81. Sano M, Saotome M, Urushida T, et al. 2012; Pulmonary arterial hypertension caused by treatment with dasatinib for chronic myeloid leukemia -critical alert-. Intern Med. 51:2337–40. DOI: 10.2169/internalmedicine.51.7472. PMID: 22975544.
crossref
82. Wang HC, Lee CS, Liu TC. 2015; Reversible dasatinib-related pulmonary arterial hypertension diagnosed by noninvasive echocardiography. Kaohsiung J Med Sci. 31:165–6. DOI: 10.1016/j.kjms.2014.11.010. PMID: 25744241.
crossref
83. Dumitrescu D, Seck C, ten Freyhaus H, Gerhardt F, Erdmann E, Rosenkranz S. 2011; Fully reversible pulmonary arterial hypertension associated with dasatinib treatment for chronic myeloid leukaemia. Eur Respir J. 38:218–20. DOI: 10.1183/09031936.00154210. PMID: 21719499.
crossref
84. Hennigs JK, Keller G, Baumann HJ, et al. 2011; Multi tyrosine kinase inhibitor dasatinib as novel cause of severe pre-capillary pulmonary hypertension? BMC Pulm Med. 11:30. DOI: 10.1186/1471-2466-11-30. PMID: 21605451. PMCID: PMC3121732.
crossref
85. Groeneveldt JA, Gans SJ, Bogaard HJ, Vonk-Noordegraaf A. 2013; Dasatinib-induced pulmonary arterial hypertension unresponsive to PDE-5 inhibition. Eur Respir J. 42:869–70. DOI: 10.1183/09031936.00035913. PMID: 24000257.
crossref
86. Nishimori M, Honjo T, Kaihotsu K, et al. 2018; Dasatinib-induced pulmonary arterial hypertension treated with upfront com-bination therapy. Case Rep Cardiol. 2018:3895197. DOI: 10.1155/2018/3895197. PMID: 29888010. PMCID: PMC5985094.
crossref
87. Galiè N, Brundage BH, Ghofrani HA, et al. 2009; Tadalafil therapy for pulmonary arterial hypertension. Circulation. 119:2894–903. DOI: 10.1161/CIRCULATIONAHA.108.839274. PMID: 19470885.
crossref
88. Fernandez Valledor A, Cepas Guillen P, Izquierdo M, et al. 2020; P1721 reversible heart right failure. Pulmonary hypertension induced by tyrosine kinase inhibitors. Eur Heart J Cardiovasc Imaging. 21(Suppl 1):jez319. 1083. DOI: 10.1093/ehjci/jez319.1083.
crossref
89. Clozel M, Breu V, Gray GA, et al. 1994; Pharmacological characterization of bosentan, a new potent orally active nonpeptide endothelin receptor antagonist. J Pharmacol Exp Ther. 270:228–35. PMID: 8035319.
90. Gregan B, Jürgensen J, Papsdorf G, et al. 2004; Ligand-dependent differences in the internalization of endothelin A and endothelin B receptor heterodimers. J Biol Chem. 279:27679–87. DOI: 10.1074/jbc.M403601200. PMID: 15075338.
crossref
91. Rubin LJ, Badesch DB, Barst RJ, et al. 2002; Bosentan therapy for pulmonary arterial hypertension. N Engl J Med. 346:896–903. DOI: 10.1056/NEJMoa012212. PMID: 11907289.
crossref
92. Dhillon S, Keating GM. 2009; Bosentan: a review of its use in the management of mildly symptomatic pulmonary arterial hypertension. Am J Cardiovasc Drugs. 9:331–50. DOI: 10.2165/11202270-000000000-00000. PMID: 19791841.
93. Humbert M, Segal ES, Kiely DG, Carlsen J, Schwierin B, Hoeper MM. 2007; Results of European post-marketing surveillance of bosentan in pulmonary hypertension. Eur Respir J. 30:338–44. DOI: 10.1183/09031936.00138706. PMID: 17504794.
crossref
94. Taçoy G, Çengel A, Özkurt ZN, Türkoğlu S. 2015; Dasatinib-induced pulmonary hypertension in acute lymphoblastic leukemia: case report. Turk Kardiyol Dern Ars. 43:78–81. DOI: 10.5543/tkda.2015.41763. PMID: 25655855.
95. Frank H, Mlczoch J, Huber K, Schuster E, Gurtner HP, Kneussl M. 1997; The effect of anticoagulant therapy in primary and anorectic drug-induced pulmonary hypertension. Chest. 112:714–21. DOI: 10.1378/chest.112.3.714. PMID: 9315805.
crossref
96. McGoon MD, Frost AE, Oudiz RJ, et al. 2009; Ambrisentan therapy in patients with pulmonary arterial hypertension who discontinued bosentan or sitaxsentan due to liver function test abnormalities. Chest. 135:122–9. DOI: 10.1378/chest.08-1028. PMID: 18812445.
crossref
97. Trow TK, Taichman DB. 2009; Endothelin receptor blockade in the management of pulmonary arterial hypertension: selective and dual antagonism. Respir Med. 103:951–62. DOI: 10.1016/j.rmed.2009.02.016. PMID: 19304472.
crossref
98. Seegobin K, Babbar A, Ferreira J, Lyons B, Cury J, Seeram V. 2017; A case of worsening pulmonary arterial hypertension and pleural effusions by bosutinib after prior treatment with dasatinib. Pulm Circ. 7:808–12. DOI: 10.1177/2045893217733444. PMID: 28914582. PMCID: PMC5703128.
crossref
99. Daccord C, Letovanec I, Yerly P, et al. 2018; First histopathological evidence of irreversible pulmonary vascular disease in dasatinib-induced pulmonary arterial hypertension. Eur Respir J. 51:1701694. DOI: 10.1183/13993003.01694-2017. PMID: 29348153.
crossref
100. Iglarz M, Binkert C, Morrison K, et al. 2008; Pharmacology of macitentan, an orally active tissue-targeting dual endothelin receptor antagonist. J Pharmacol Exp Ther. 327:736–45. DOI: 10.1124/jpet.108.142976. PMID: 18780830.
crossref
101. Cadenas-Menéndez S, Álvarez Vega P, Oterino Manzanas A, et al. 2020; Evolution of patients with pulmonary arterial hypertension starting macitentan after the discontinuation of other endothelin-receptor antagonists: results of a retrospective study. Am J Cardiovasc Drugs. 20:481–7. DOI: 10.1007/s40256-019-00392-y. PMID: 31879844.
crossref
102. Rubin L, Pulido T, Channick R, et al. 2012; Effect of macitentan on morbidity and mortality in pulmonary arterial hypertension (PAH): results from the SERAPHIN trial. Chest (Meeting Abstracts). 142(Suppl):1026A. DOI: 10.1378/chest.1456207.
crossref
103. Wong AK, Channick RN. 2019; Safety and tolerability of macitentan in the management of pulmonary arterial hypertension: an update. Drug Healthc Patient Saf. 11:71–85. DOI: 10.2147/DHPS.S173050. PMID: 31564989. PMCID: PMC6731963.
104. Toya T, Nagatomo Y, Kagami K, Adachi T. 2019; Dasatinib-induced pulmonary arterial hypertension complicated with scleroderma: a case report. Eur Heart J Case Rep. 3:ytz025. DOI: 10.1093/ehjcr/ytz025. PMID: 31020267. PMCID: PMC6439368.
crossref
105. Dupuis J, Hoeper MM. 2008; Endothelin receptor antagonists in pulmonary arterial hypertension. Eur Respir J. 31:407–15. DOI: 10.1183/09031936.00078207. PMID: 18238950.
crossref
106. Galiè N, Hoeper MM, Gibbs JS, Simonneau G. 2011; Liver toxicity of sitaxentan in pulmonary arterial hypertension. Eur Respir J. 37:475–6. DOI: 10.1183/09031936.00194810. PMID: 21282816.
107. Lee WT, Kirkham N, Johnson MK, Lordan JL, Fisher AJ, Peacock AJ. 2011; Sitaxentan-related acute liver failure in a patient with pulmonary arterial hypertension. Eur Respir J. 37:472–4. DOI: 10.1183/09031936.00091610. PMID: 21282815.
crossref
108. Friedman R, Mears JG, Barst RJ. 1997; Continuous infusion of prostacyclin normalizes plasma markers of endothelial cell injury and platelet aggregation in primary pulmonary hyper-tension. Circulation. 96:2782–4. DOI: 10.1161/01.CIR.96.9.2782. PMID: 9386137.
crossref
109. Demling RH, Smith M, Gunther R, Gee M, Flynn J. 1981; The effect of prostacyclin infusion on endotoxin-induced lung injury. Surgery. 89:257–63. PMID: 7006136.
110. Jacobs W, Vonk-Noordegraaf A. 2009; Epoprostenol in pulmonary arterial hypertension. Expert Opin Drug Metab Toxicol. 5:83–90. DOI: 10.1517/17425250802622962. PMID: 19236231.
crossref
111. Jones DK, Higenbottam TW, Wallwork J. 1987; Treatment of primary pulmonary hypertension intravenous epoprostenol (prostacyclin). Br Heart J. 57:270–8. DOI: 10.1136/hrt.57.3.270. PMID: 3552006. PMCID: PMC1216424.
crossref
112. Rubin LJ, Mendoza J, Hood M, et al. 1990; Treatment of primary pulmonary hypertension with continuous intravenous pro-stacyclin (epoprostenol). Results of a randomized trial. Ann Intern Med. 112:485–91. DOI: 10.7326/0003-4819-112-7-485. PMID: 2107780.
113. Rich S, McLaughlin VV. 1999; The effects of chronic prostacyclin therapy on cardiac output and symptoms in primary pulmonary hypertension. J Am Coll Cardiol. 34:1184–7. DOI: 10.1016/S0735-1097(99)00320-4. PMID: 10520810.
crossref
114. Barst RJ, Rubin LJ, Long WA, et al. 1996; A comparison of continuous intravenous epoprostenol (prostacyclin) with conventional therapy for primary pulmonary hypertension. N Engl J Med. 334:296–301. DOI: 10.1056/NEJM199602013340504. PMID: 8532025.
crossref
115. Helgeson S, Imam JS, Burger C. 2016; Severe PAH secondary to dasatinib: PAH treatment required? Chest (Meeting Abstracts). 150:1218A. DOI: 10.1016/j.chest.2016.08.1327.
crossref
116. Helgeson S. 2016; Pulmonary arterial hypertension: case report. Reactions. 1632:107–17. DOI: 10.1007/s40278-016-24070-2. PMID: 27057843. PMCID: PMC4998759.
117. Badesch DB, Tapson VF, McGoon MD, et al. 2000; Continuous intravenous epoprostenol for pulmonary hypertension due to the scleroderma spectrum of disease. A randomized, controlled trial. Ann Intern Med. 132:425–34. DOI: 10.7326/0003-4819-132-6-200003210-00002. PMID: 10733441.
118. Kallen AJ, Lederman E, Balaji A, et al. 2008; Bloodstream infections in patients given treatment with intravenous prostanoids. Infect Control Hosp Epidemiol. 29:342–9. DOI: 10.1086/529552. PMID: 18462147.
crossref
119. Chin KM, Channick RN, de Lemos JA, Kim NH, Torres F, Rubin LJ. 2009; Hemodynamics and epoprostenol use are associated with thrombocytopenia in pulmonary arterial hypertension. Chest. 135:130–6. DOI: 10.1378/chest.08-1323. PMID: 18719056.
crossref
120. Skoro-Sajer N, Lang I, Naeije R. 2008; Treprostinil for pulmonary hypertension. Vasc Health Risk Manag. 4:507–13. DOI: 10.2147/VHRM.S2477. PMID: 18827901. PMCID: PMC2515411.
121. Lang I, Gomez-Sanchez M, Kneussl M, et al. 2006; Efficacy of long-term subcutaneous treprostinil sodium therapy in pulmonary hypertension. Chest. 129:1636–43. DOI: 10.1378/chest.129.6.1636. PMID: 16778286.
crossref
122. Tapson VF, Gomberg-Maitland M, McLaughlin VV, et al. 2006; Safety and efficacy of IV treprostinil for pulmonary arterial hypertension: a prospective, multicenter, open-label, 12-week trial. Chest. 129:683–8. DOI: 10.1378/chest.129.3.683. PMID: 16537868.
123. Benza RL, Rayburn BK, Tallaj JA, Pamboukian SV, Bourge RC. 2008; Treprostinil-based therapy in the treatment of moderate-to-severe pulmonary arterial hypertension: long-term efficacy and combination with bosentan. Chest. 134:139–45. DOI: 10.1378/chest.07-2111. PMID: 18403673.
crossref
124. Laliberte K, Arneson C, Jeffs R, Hunt T, Wade M. 2004; Pharmacokinetics and steady-state bioequivalence of treprostinil sodium (Remodulin) administered by the intravenous and subcutaneous route to normal volunteers. J Cardiovasc Pharmacol. 44:209–14. DOI: 10.1097/00005344-200408000-00010. PMID: 15243302.
crossref
125. Sadushi-Koliçi R, Skoro-Sajer N, Zimmer D, et al. 2012; Long-term treatment, tolerability, and survival with sub-cutaneous treprostinil for severe pulmonary hypertension. J Heart Lung Transplant. 31:735–43. DOI: 10.1016/j.healun.2012.02.025. PMID: 22480725.
crossref
126. Gomberg-Maitland M, Tapson VF, Benza RL, et al. 2005; Transition from intravenous epoprostenol to intravenous treprostinil in pulmonary hypertension. Am J Respir Crit Care Med. 172:1586–9. DOI: 10.1164/rccm.200505-766OC. PMID: 16151039.
crossref
127. Rubenfire M, McLaughlin VV, Allen RP, et al. 2007; Transition from IV epoprostenol to subcutaneous treprostinil in pulmonary arterial hypertension: a controlled trial. Chest. 132:757–63. DOI: 10.1378/chest.06-2118. PMID: 17400684.
128. Vachiéry JL, Hill N, Zwicke D, Barst R, Blackburn S, Naeije R. 2002; Transitioning from i.v. epoprostenol to subcutaneous treprostinil in pulmonary arterial hypertension. Chest. 121:1561–5. DOI: 10.1378/chest.121.5.1561. PMID: 12006444.
crossref
129. Voswinckel R, Enke B, Reichenberger F, et al. 2006; Favorable effects of inhaled treprostinil in severe pulmonary hypertension: results from randomized controlled pilot studies. J Am Coll Cardiol. 48:1672–81. DOI: 10.1016/j.jacc.2006.06.062. PMID: 17045906.
130. Simonneau G, Barst RJ, Galie N, et al. 2002; Continuous subcutaneous infusion of treprostinil, a prostacyclin analogue, in patients with pulmonary arterial hypertension: a double-blind, randomized, placebo-controlled trial. Am J Respir Crit Care Med. 165:800–4. DOI: 10.1164/ajrccm.165.6.2106079. PMID: 11897647.
131. Hoeper MM, Schwarze M, Ehlerding S, et al. 2000; Long-term treatment of primary pulmonary hypertension with aerosolized iloprost, a prostacyclin analogue. N Engl J Med. 342:1866–70. DOI: 10.1056/NEJM200006223422503. PMID: 10861321.
crossref
132. Olschewski H, Simonneau G, Galiè N, et al. 2002; Inhaled iloprost for severe pulmonary hypertension. N Engl J Med. 347:322–9. DOI: 10.1056/NEJMoa020204. PMID: 12151469.
crossref
133. Krishnan U, Takatsuki S, Ivy DD, et al. 2012; Effectiveness and safety of inhaled treprostinil for the treatment of pulmonary arterial hypertension in children. Am J Cardiol. 110:1704–9. DOI: 10.1016/j.amjcard.2012.07.037. PMID: 22917554. PMCID: PMC3508003.
crossref
134. Barst RJ, McGoon M, McLaughlin V, et al. 2003; Beraprost therapy for pulmonary arterial hypertension. J Am Coll Cardiol. 41:2119–25. DOI: 10.1016/S0735-1097(03)00463-7. PMID: 12821234.
crossref
135. Sorensen LM, Wehland M, Kruger M, et al. 2017; A special focus on selexipag-treatment of pulmonary arterial hypertension. Curr Pharm Des. 23:5191–9. DOI: 10.2174/1381612823666170908114227. PMID: 28891448.
crossref
136. Sitbon O, Channick R, Chin KM, et al. 2015; Selexipag for the treatment of pulmonary arterial hypertension. N Engl J Med. 373:2522–33. DOI: 10.1056/NEJMoa1503184. PMID: 26699168.
crossref
137. Kuwano K, Hashino A, Noda K, Kosugi K, Kuwabara K. 2008; A long-acting and highly selective prostacyclin receptor agonist prodrug, 2-{4-[(5,6-diphenylpyrazin-2-yl)(isopropyl)amino] butoxy}-N-(methylsulfonyl)acetamide (NS-304), ameliorates rat pulmonary hypertension with unique relaxant responses of its active form, {4-[(5,6-diphenylpyrazin-2-yl)(isopropyl) amino]butoxy}acetic acid (MRE-269), on rat pulmonary artery. J Pharmacol Exp Ther. 326:691–9. DOI: 10.1124/jpet.108.138305. PMID: 18552131.
138. Simonneau G, Hwang LJ, Teal S, Galie N. 2012; Incidence of subdural hematoma in patients with pulmonary arterial hypertension (PAH) in two randomized controlled clinical trials. Eur Respir J. 40(Suppl):P941.
139. Rich S, Brundage BH. 1987; High-dose calcium channel-blocking therapy for primary pulmonary hypertension: evidence for long-term reduction in pulmonary arterial pressure and regression of right ventricular hypertrophy. Circulation. 76:135–41. DOI: 10.1161/01.CIR.76.1.135. PMID: 2954725.
crossref
140. Galiè N, Hoeper MM, Humbert M, et al. 2009; Guidelines for the diagnosis and treatment of pulmonary hypertension: the Task Force for the Diagnosis and Treatment of Pulmonary Hypertension of the European Society of Cardiology (ESC) and the European Respiratory Society (ERS), endorsed by the International Society of Heart and Lung Transplantation (ISHLT). Eur Heart J. 30:2493–537. DOI: 10.1093/eurheartj/ehp297. PMID: 19713419.
141. Humbert M, Sitbon O, Simonneau G. 2004; Treatment of pulmonary arterial hypertension. N Engl J Med. 351:1425–36. DOI: 10.1056/NEJMra040291. PMID: 15459304.
crossref
142. Montani D, Savale L, Natali D, et al. 2010; Long-term response to calcium-channel blockers in non-idiopathic pulmonary arterial hypertension. Eur Heart J. 31:1898–907. DOI: 10.1093/eurheartj/ehq170. PMID: 20543192.
crossref
143. Galiè N, Corris PA, Frost A, et al. 2013; Updated treatment algorithm of pulmonary arterial hypertension. J Am Coll Cardiol. 62:D60–72. DOI: 10.1016/j.jacc.2013.10.031. PMID: 24355643.
crossref
144. Barst RJ, Gibbs JSR, Ghofrani HA, et al. 2009; Updated evidence-based treatment algorithm in pulmonary arterial hypertension. J Am Coll Cardiol. 54(Suppl 1):S78–84. DOI: 10.1016/j.jacc.2009.04.017. PMID: 19555861. PMCID: PMC3686287.
crossref
145. Rich S, Kaufmann E, Levy PS. 1992; The effect of high doses of calcium-channel blockers on survival in primary pulmonary hypertension. N Engl J Med. 327:76–81. DOI: 10.1056/NEJM199207093270203. PMID: 1603139.
crossref
146. Packer M, Medina N, Yushak M, Wiener I. 1984; Detrimental effects of verapamil in patients with primary pulmonary hyper-tension. Br Heart J. 52:106–11. DOI: 10.1136/hrt.52.1.106. PMID: 6743418. PMCID: PMC481593.
crossref
147. Orlikow E, Weatherald J, Hirani N. 2019; Dasatinib-induced pulmonary arterial hypertension. Can J Cardiol. 35:1604e1–e3. DOI: 10.1016/j.cjca.2019.08.002. PMID: 31590985.
crossref
148. Schilz R, Rich S. 2017; Calcium channel blocker therapy: when a drug works, it works. When it doesn't, it doesn't. Adv Pulm Hypertens. 15:184–9. DOI: 10.21693/1933-088X-15.4.184.
crossref

Fig. 1
Management of dasatinib-induced pleural effusion.
br-56-4-229-f1.tif
Table 1
FDA approved pharmacological classes for treatment of PAH.
Class Drug Rout of administration Dose
Prostacyclin derivatives Epoprostenol IV Initial dose of 2 ng kg-1min-1 Iv infusion, titrated by 1–2 ng kg-1min-1q 15 min if tolerated
Iloprost Inhaled 2.5 μg inhaled, if tolerated then 5 μg, 6–9 times a day PRN; Maintenance: 2.5–5 μg dose-1 (max: 45 μg daily)
Treprostinil PO PO: 0.125 mg TID or 0.25 mg BID, titrated by 0.125 mg TID every 3–4 days
Continuous IV or SC infusion IV or SC infusion: 1.25 ng kg-1min-1 titrated by no more than 1.25 ng kg-1min-1per wk based on clinical response; after 4 wk, titrated by no more than 2.5 ng kg-1min-1 per wk based on clinical response
Endothelin receptor antagonists Bosentan Oral 125 mg twice daily
Ambrisentan Oral 5 or 10 mg once daily
Macitentan Oral 10 mg once daily
Phosphodiesterase type-5 inhibitors Sildenafil Oral 20 mg TID
IV Injection
Tadalafil Oral 40 mg once daily
Soluble cGMP stimulators Riociguat Oral 0.5–1.0 mg TID (titrated by 0.5 mg every 2 wk as tolerated to maximum dose 2.5 mg)
Prostacyclin receptor agonists Selexipag Oral 200 mg twice daily, titrated as tolerated to maximum dose of 16,000 mg twice daily

Abbreviations: cGMP, Cyclic guanosine monophosphate; FDA, Food and Drug Administration; h, hour; IV, Intravenous; PAH, pulmonary arterial hypertension; SC, subcutaneous.

Table 2
Cases of dasatinib-induced PAH and their pharmacotherapy.
Study N of participants/diagnosis Age, yr/
gender, M or F
Time from dasatinib initiation to PAH diagnosis (mo) DASA dose, mg/day Treatment
line of DASA
Concomitant PE Intervention Improved items
Jose et al. (2017) [64] 1, CML 61, M 26 140 Second Yes DASA D/C
Tad 20 mg QD and Amb 5 mg daily. The Tad was up-titrated over a period of 4 wk to 40 mg QD, followed by an up titration of Amb to 10 mg QD over the following 4 wk
After 4 mo,
mPAP
PCWP
PVR
6-MWD
WHO FC
Ibrahim et al. (2019) [62] 1, CML 46, F 120 70 Second Yes DASA D/C
Amb 5 mg daily+Tad 20 mg
QD
After 1 wk,
PAP
Orlandi et al. (2012) [80] 1, CML 53, F 31 100 Second No DASA D/C
Sil 20 mg
TID
After 2 mo,
WHO FC
PAP
6-MWD
Sano et al. (2012) [81] 1, CML 61, F 27 140 Second Yes DASA D/C
Sil 60 mg QD
After 1 mo,
WHO FC
RVSP
NT-pro BNP
PAP
Wang et al. (2015) [82] 1, CML 33, M 63 100 Second No DASA D/C
Sil
After 3 mo,
PASP
Taçoy et al.(2015) [94] 1, ALL 50, M 24 140 Second Yes DASA D/C
Bos 62.5 mg BID and in 2 wk increased to 125 mg BID
After 1 mo,
NYHA FC
After 9 mo,
Pro BNP
6-MWD
Groeneveldt et al. (2013) [85] 1, CML 57, M 37 70 Second No Sil
DASA D/C
The patient did not improve in NYHA FC class by sildenafil and diuretics.
3 mo after substitution DASA with NIL,
NYHA FC after start NIL
Nishimori et al. (2018) [86] 1, CML 24, M 48 100 Second Yes DASA D/C
Sil 20 mg
TID+Bos 62.5 mg BID
After 1 mo,
WHO FC
PAP
BNP
Helgeson et al. (2016) [115] 1, CML 30, F 36 NR Second Yes DASA D/C
EPO 20 ng kg-1 min-1 for 5 mo, then EPO 4 ng kg-1 min-1 for 5 mo and discontinuation with mild rebound of MPAP, therefore, Sil was initiated
After 1 wk EPO,
Dyspnea
Toya et al. (2019) [104] 1, CML and scleroderma 63, M 36 100 Second Yes DASA D/C
Tad 40 mg QD+Mac 10 mg QD+Sel 1.2 mg
BID
After 1 mo,
mPAP
PVR
6-MWD
Buchelli et al. (2014) [71] 1, CML 50, M 48 100 Second Yes DASA D/C
Sil 20 mg TID
After 21 mo,
WHO FC
RVSP
NT-pro BNP
mPAP
PVR
6-MWD
CO
CI
Seegobin et al. (2017) [98] 1, CML 52, M 48 NR Second Yes DASA D/C
Amb
NR,
Symptoms as well as effusions improved
Daccord et al. (2018) [99] 1, CML 32, M 36 NR Third Yes DASA D/C
PDE-5 inhibitor+ERA
NR,
NYHA FC
mPAP
6-MWD
PVR
CI
Dumitrescu et al. (2011) [83] 1, CML 47, M 72 100 Second Yes DASA D/C
Sil
After 2 mo,
WHO FC
PAP
CO
Skride et al. (2017) [70] 1, CML 67, M 42 100 Second Yes DASA D/C
Sil 20 mg TID
NR,
mPAP
6-MWD
PVR
CO
Orlikow et al. (2019) [147] 1, CML 73, F 9 NR Second Yes DASA D/C
Nif 30 mg QD
After 12 mo,
CO
CI
PVR
Hennigs et al. (2011) [84] 1, CML 70, M 32 140 Second Yes DASA D/C
Sil 20 mg TID
After 10 mo,
CO
RVSP
NT-proBNP
6-MWD
Mpap
WHO FC
PVR
Hong et al. (2015) [61] 2, CML 43, M 69 140
Second Yes DASAD/C
Sil+CCB+Diuretics
NR,
NYHA FC
PAP
RVSP
52, M 38 140 Second Yes DASA D/C
Sil 25 mg QD
NR,
RVSP
BNP
6-MWD
Montani et al. (2012) [15] 3, CML 74, F 33 100 Second Yes DASA D/C
CCB for 6 mo, then stopped
After 3 mo,
NYHA FC,
mPAP
6-MWT
PVR
BNP
29, F 36 100 Second Yes DASA D/C
Bos
After 2 mo,
NYHA FC
After 6 mo,
mPAP
6-MWT
PVR
39, F 34 100 Second Yes DASA D/C
Bos
After 1 mo,
NYHA FC

Abbreviations: 6-MWD, 6-minute walk distance; ALL, acute lymphoblastic leukemia; Amb, ambrisentan; BID, two times a day; BNP, b-type natriuretic peptide; Bos, bosentan; CCB, calcium channel blocker; CI, cardiac index; CML, chronic myeloid leukemia; CO, cardiac output; DASA, dasatinib; D/C, discontinuation; EPO, epoprostenol; ERA, endothelin receptor-1 antagonist; F, female; FC, functional classification; M, male; Mac, macitentan; mPAP, mean pulmonary artery pressure; Nif, nifedipine; NIL, nilotinib; NT-pro BNP, N-terminal pro b-type natriuretic peptide; NYHA, New York heart association; PAH, pulmonary arterial hypertension; PAP, pulmonary artery pressure; PASP, pulmonary artery systolic pressure; PCWP, pulmonary capillary wedge pressure; PDE-5, phosphodiesterase-5; PE, pulmonary embolism; Pro BNP, pro hormone b-type natriuretic peptide; PVR, pulmonary vascular resistance; QD, once a day; RVSP, right ventricular systolic pressure; Sel, selexipag; Sil, sildenafil; Tad, tadalafil; TID, three times a day; WHO, world health organization; WU, wood unit.

TOOLS
Similar articles