Journal List > Korean J Hematol > v.41(4) > 1032689

Yi, Lim, Kim, Park, Moon, Lee, Nahm, and Kim: Ten-year Experience on Acute Promyelocytic Leukemia at Inha University Hospital

Abstract

Background:

Acute promyelocytic leukemia (APL) is a distinct subtype of acute myeloid leukemia in its morphology as well as molecular or genetic profiles, conferring a good prognosis owing to the active roles of all-trans-retinoic acid (ATRA) and anthracyclines.

Methods:

Patients diagnosed as APL from March 1997 to April 2006 were analyzed on their clinical features, laboratory profiles, methods of treatment including remission induction, consolidation and maintenance, treatment outcomes, and treatment-related morbidity.

Results:

Chemotherapy naïve were all the 12 patients in our study consisting of 3 males and 9 females. All patients showed typical morphologic feature of APL with cytogenetic abnormality, t(15;17), and PML/RARα fusion gene was confirmed in 10 patients by FISH or PCR. The combination of cytarabine with daunorubicin (n=2) or idarubicin (n=9) was used as an induction regimen with concurrent ATRA administration. For consolidation therapy, cytarabine with anthracycline (n=4) or idarubicin monotherapy (n=8) was used with ATRA. Cytogenetic and molecular remissions were documented after induction chemotherapy (n=11) or first consolidation therapy (n=1). Maintenance therapy with ATRA was done in 11 patients. CR was obtained in 12 patients, with median remission duration of 30.5+ months (range 2 to 86+) at a median follow up duration of 33.5+ months (range 4 to 89+). One patient relapsed after completion of maintenance therapy and died of infection during reinduction chemotherapy.

Conclusion:

Herein is the report of ten years’ experience of our hospital in the treatment of APL with favorable results as seen by high CR rate and fewer complications.

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Fig. 1
The clinical outcome of chemotherapy.
kjh-41-289f1.tif
Fig. 2
ATRA syndrome. Diffuse bilateral pulmonary infiltration 20 days after ATRA administration (A, B), and disappearance after 20 days’ parenteral steroid treatment (C).
kjh-41-289f2.tif
Table 1.
The schedule of chemotherapeutic regimen
  Induction     Consolidation  
1) AI     1) I    
  Ara-C 100mg/m2/d D1~7   Idarubicin 12mg/m2/d D1~3
  Idarubicin 12mg/m2/d D1~3 2) AD    
2) AD       Ara-C 1g/m2/d D1~7
  Ara-C 100mg/m2/d D1~7   Daunorubicin 45mg/m2/d D1~3
  Daunorubicin 45mg/m2/d D1~3 3) MA    
3) ATRA∗ 45mg/m2/d Max.   Ara-C 1g/m2/d D1~7
    100 days   Mitoxantrone 12mg/m2/d D1~3
      4) M    
        Mitoxantrone 12mg/m2/d D1~3

∗ATRA was concurrently given with remission induction chemotherapy except for one case where ATRA monotherapy was used for remission induction. The maintenance protocol consisted of ATRA at 40mg/m2 for 2 weeks every 8 weeks for 2 years used in all patients except one.

Table 2.
The characteristics of patients
  No. of patients (total n=12)
Sex  
Male:Female 3:9
Age (median/range) 39/26~59
DIC (clinical/laboratory) 10/12
Fever at diagnosis 10
Hematologic profile (median/range)
Leukocyte (/μL) 2,100 (1,200~30,100)
Hemoglobin (g/dL) 8.5 (5.2~14)
Platelet (/μL) 37,000 (4,000~97,000
t(15:17) 12
PML-RARα (PCR or FISH) at diagnosis 10/11
 
Table 3.
The cytogenetic and molecular changes during chemotherapy
kjh-41-289t3.tif
Table 4.
The result of chemotherapy
  No. of patients (total n=12)
CR after induction or reinduction 12
  Median month/range
Follow-up duration 33.5/(4~89)
CR duration 30.5/(2~86)
Overall survival duration 5~89
Median survival Not reached
Table 5.
Transfusion requirement during chemotherapy
  RBC (pack) Platelet (unit)
Induction (median/range) 8/(4~30) 80/(44~345)
Total (median/range) 16.5/(9~34) 196.5/(140~461)
Table 6.
The complications during chemotherapy
  No. of events
ATRA-related (total 7 patients) 13
  ATRA syndrome 2
  Fever 3
  Rash 3
  Leukocytosis 1
  Arthritis 1
  Vomiting/diarrhea 1
Fever (event/total chemotherapy) 38/45
Infection, microbiolocally proven 13
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