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Introduction
Uterine leiomyosarcoma (LMS) is a rare uterine cancer that accounts for approximately 1% of all uterine cancers [12]. However, because of its aggressive biology and resistance to chemotherapy, LMS causes approximately 70% of deaths caused by uterine malignant tumors [34]. The symptoms and presenting characteristics of uterine LMS are almost indistinguishable from those of uterine leiomyoma [1]. Palpable mass and abnormal vaginal bleeding followed by weight loss and general weakness are the most common symptoms of uterine LMS [56]. Intraoperatively, it is difficult to differentiate between LMS and leiomyoma based on visible evidence alone [7], and uterine LMS is often diagnosed by histologic evaluation of tumor specimens.
Surgical removal of tumors, including hysterectomy and/or bilateral salpingo-oophorectomy, is the standard management for uterine LMS. However, surgical staging is regarded as less important because uterine LMS is known to have early hematogenous metastasis and rare lymphatic spread [8]. Recently, there has been an increase in the frequency of adjuvant chemotherapy and radiation therapy for the treatment of uterine LMS. However, adjuvant treatment has not shown a definite survival advantage [3].
Although in most cases, the tumor is limited to the uterus, it remains difficult to predict the disease course of uterine LMS. Stage is the strongest predictor of survival. Various other prognostic factors have previously been suggested for uterine LMS, but these remain controversial and the available data is limited [910]. We aimed to determine the possible prognostic factors for recurrence, overall survival (OS), and survival after recurrence in patients with uterine LMS.
Materials and methods
1. Patients and treatment
The medical records of 50 patients with uterine LMS, who were diagnosed and treated at Samsung Medical Center from 2001 to 2017, were retrospectively reviewed. Per the routine protocol in patients with uterine LMS, patients underwent total hysterectomy and salpingo-oophorectomy (either bilateral or unilateral). The decision to perform adjuvant therapy (chemotherapy/radiation therapy) was made on the basis of the physician's opinion and patient's situation. To treat recurrent disease, chemotherapy, radiotherapy, and/or surgical resection of tumor were considered, if feasible. Available histological slides were also reviewed by a gynecologic pathologist. LMS was histologically defined by the presence of 2 of the following 3 criteria: 1) significant nuclear atypia, 2) >10 mitotic counts per 10 high-power field (HPF), and 3) coagulative tumor cell necrosis [11]. The modified 2009 International Federation of Gynecology and Obstetrics (FIGO) staging for LMS was used.
Clinicopathologic, surgical, and survival data were retrospectively gathered from electronic medical records. Prognostic variables that were included in this study were age at primary diagnosis, tumor suspected as leiomyoma with clinical characteristics before surgery, FIGO stage, residual disease status after primary surgery, tumor size, symptoms at diagnosis, grade, nuclear atypia, mitotic count (per 10 HPF), history of adjuvant therapy after primary surgery (chemotherapy/radiotherapy), recurrence pattern (peritoneal/hematogenous), and treatment after recurrence. Characteristics were assigned to categories for descriptive purposes and statistical analysis.
Tumor size was recorded on the basis of the maximum dimension of the tumor at pathologic analysis. The tumor grade, nuclear atypia, and mitotic count were recorded on the basis of final pathologic reports. Symptoms at diagnosis were limited to those related to the uterine mass at the time of diagnosis. Recurrence patterns were categorized into peritoneal and hematogenous metastases. Peritoneal recurrences were defined as the recurrence of metastatic lesions in the peritoneum of the pelvis and abdominal areas. Hematogenous recurrences were defined as visceral metastases such as those in the liver and lung parenchyma.
Recurrence-free survival (RFS) was defined as the time of initial diagnosis to the date of recurrence, death, or loss to follow-up. OS was described as the time between diagnosis and the patient's death or loss to follow-up. Survival after recurrence was described as the time between the diagnosis of recurrence and the patient's death or loss to follow-up.
2. Statistical analysis
Summary statistics were used to describe the data. Median (range) or mean (standard deviation) was used to describe continuous variables. Categorical variables were presented as frequencies (percentages). After confirming normal distributions using the Shapiro-Wilk test, the Mann-Whitney test was used to compare median values, and the Student's t-test was used to compare mean values. Categorical variables were presented as frequencies (percentages). Fisher's exact test or χ2 test was used to analyze the distribution of characteristics. Survival curves were drawn by the Kaplan-Meier method and were compared using the log-rank test. Cox proportional hazards model was used for univariate and multivariate analyses to evaluate the prognostic significance of clinicopathologic features for RFS, OS, and survival after recurrence. For multivariate analysis, a stepwise backward elimination method was used. Variables that were significantly associated with RSF, OS, and survival after recurrence with a significance level of P<0.10 in univariate analysis were selected for possible inclusion in multivariate logistic regression models, as it was previously suggested that this value could be used as an appropriate threshold [12]. Multivariate P-values were used to represent the significance of each feature. A 95% confidence interval (CI) was used to quantify the correlation between survival time and each independent feature. All P-values were 2-sided, and P-values <0.05 were regarded as statistically significant. All statistical analyses were accomplished using IBM SPSS ver. 21.0 (IBM Corp., Armonk, NY, USA).
Results
The clinicopathologic characteristics of 50 patients with uterine LMS are presented in Table 1. At the time of analysis, 30 patients (60.0%) experienced recurrence, and 16 patients (32.0%) died within a median follow-up period of 21 (range, 3–99) months. Median age was 48 (range, 31–72) years, and 60.0% of the patients had stage I disease. Median tumor size was 10 (range, 3.0–29.0) cm, and moderate atypia was the most common feature (54.0%). Peritoneal recurrence was more common than hematogenous recurrence (66.7% vs. 33.3%) among patients with recurrence, and lymphatic recurrence was not observed in our data. Upon comparing characteristics between patients with and without recurrence, age, grade, mitotic count (10 HPF), and type of adjuvant therapy after primary surgery showed significant differences between the 2 groups (Table 1).
Table 1
Characteristics of study cohorts (n=50)
Univariate and multivariate analyses were performed to identify prognostic factors for RFS, OS, and survival after recurrence. In analysis for RFS (Table 2), age, stage, tumor suspected as leiomyoma before surgery, residual status after primary surgery, tumor size, grade, nuclear atypia, mitotic count, and history of adjuvant chemotherapy/radiotherapy were significant variables in univariate analysis. Among these factors, age (hazard ratio [HR], 1.091; 95% CI, 1.045–1.140; P<0.001), residual disease (HR, 5.066; 95% CI, 1.880–13.651; P<0.001), mitotic count (>10/10 HPF, HR, 3.976; 95% CI, 1.420–11.131; P=0.009), and history of radiotherapy (HR, 0.209; 95% CI, 0.076–0.578; P=0.003) were significant variables in multivariate analysis. Fig. 1A and B show Kaplan–Meier curves for the time influenced by significant prognostic factors, residual disease status, and mitotic count.
Table 2
Univariate and multivariate Cox proportional hazards analysis for recurrence-free survival to adjust risk associated with prognostic clinical features (n=50)
Fig. 1
Kaplan-Meier curve considering the influence of significant prognostic factors for recurrence-free survival (A, B), overall survival (C, D), and survival after recurrence (E, F).
Significant prognostic factors for OS in univariate analysis were stage, residual disease after primary surgery, tumor size, grade, nuclear atypia, mitotic count, and adjuvant chemotherapy (Table 3). In multivariate analysis, the presence of residual disease after primary surgery (HR, 3.740; 95% CI, 1.170–11.956; P=0.026) and severe nuclear atypia (HR, 6.041; 95% CI, 1.977–18.465; P=0.002) were significant prognostic factors associated with OS. Fig. 1C and D show survival curves influenced by residual disease status and nuclear atypia.
Table 3
Univariate and multivariate Cox proportional hazards analysis for overall survival to adjust risk associated with prognostic clinical features (n=50)
For analysis of survival after recurrence, only patients with recurrence were assessed (n=30). In univariate analysis, nuclear atypia was a significant factor (Table 4). In multivariate analysis, the presence of residual disease status (HR, 11.304; 95% CI, 2.009–65.598; P=0.006), severe nuclear atypia (HR, 17.237; 95% CI, 2.902–102.384; P=0.002), and hematogenous recurrence (HR, 4.189; 95% CI, 1.032–17.000; P=0.045) were significantly associated with worse prognosis in survival after recurrence. The survival curve for survival after recurrence is shown in Fig. 1E and F.
Table 4
Univariate and multivariate Cox proportional hazards analysis for survival after recurrence to adjust risk associated with prognostic clinical features (n=30)
Discussion
In our study, retrospective analysis of 50 patients with uterine LMS demonstrated possible prognostic factors for RFS, OS, and survival after recurrence. Age, residual disease status, mitotic count, and history of adjuvant radiotherapy were significant factors for RFS. Residual disease status and nuclear atypia were significant factors for OS, while residual disease status, nuclear atypia, and recurrence pattern were significant factors for survival after recurrence. Notably, complete resection of tumor at primary surgery was significantly associated with RFS, OS, and survival after recurrence.
A number of studies on the prognostic factors for uterine LMS have previously been published. The most important prognostic factor for survival in uterine LMS remains tumor stage at diagnosis. In 2009, FIGO presented a new classification for uterine LMS that includes tumor size, extrauterine involvement, and invasion to abdominal tissue [6]. In a previous study of Surveillance, Epidemiology, and End Results data of patients with uterine LMS from 2000 to 2012, almost half of patients were stage I, 14% were stage II and III, and 31% were stage IV [13]. Survival outcomes of uterine LMS are poor regardless of stage with 5-year disease-free survival of 65.7% in total the cohort [14]. In addition to FIGO stage, other reported prognostic factors include age, tumor size, mitotic index, and lymphovascular invasion [1015161718]. Not all of these factors are included in current staging, yet they are related to prognosis.
In a study analyzing prognostic factors using the National Cancer Database [19], surgical resection remained the best effective management for uterine LMS. In the current study, stage-defining variables and other factors were used to analyze prognostic factors, and residual tumor status at primary surgery was also associated with RFS, OS, and survival after recurrence. With regard to surgical resection of uterine LMS, total hysterectomy with/without bilateral salpingo-oophorectomy is the standard treatment for patients with uterine-confined disease. Tumor removal should be en bloc, with an effort to avoid intraoperative rupture, morcellation, or spillage in the peritoneal cavity. Despite having metastatic disease, patients with both intraperitoneal and extraperitoneal disease are considered to be appropriate candidates for surgical resection due to limited systemic treatment options. In a previous retrospective study performed at the Memorial Sloan Kettering Cancer Center showed that optimal surgical resection was associated with improved progression-free survival [20]. Patients with hematogenous metastasis can also be considered as candidates for surgical resection. Several studies showed improved survival outcomes after pulmonary metastasectomy, and pulmonary metastasectomy is an effective option for selected patients with metastatic uterine LMS [21222324]. According to previous studies, surgical resection for uterine LMS should be performed for better survival outcomes in the appropriate candidates.
For uterine LMS, the effect of adjuvant therapy is still unclear due to its poor efficacy [25]. In our results, administration of adjuvant radiotherapy was associated with improved RFS. However, this was not significant in long-term survival, and survival advantage may not persist. Patients who underwent adjuvant chemotherapy showed poor survival in univariate analysis for RFS and OS, but not in multivariate analysis, probably because chemotherapy is for patients with advanced stage or distant metastasis. We cannot further support results regarding adjuvant therapy because the results are based on a small number of patients.
Diagnostic evaluation of uterine LMS and distinguishing between benign leiomyoma and LMS is difficult because they often have similar symptoms. Abnormal uterine bleeding, pelvic pain or palpation of abdominal mass may present in both diseases. Also, there are currently no validated clinical or radiologic criteria to differentiate between leiomyoma and LMS, as the final diagnosis is made histopathologically after surgery. In our analysis, we determined whether a tumor suspected as LMS before surgery with clinical characteristics can be a useful prognostic factor in LMS. It was only significant in univariate analysis for RFS, but not in multivariate analysis. It was not significantly related to survival in our results. With respect to tumor marker for LMS, serum lactate dehydrogenase level is known to be elevated in some patients [26]. In our study, we were able to analyze only serum cancer antigen (CA)-125 levels due to limited data and the retrospective nature of this study. There was a median initial serum CA-125 level difference between the recurrent and non-recurrent group, but it was not statistically significant. Serum CA-125 elevation was not observed at relapse. We did not find a relationship between CA-125 level and the prognosis of LMS patients from our data, which is similar to a previous study that showed that CA-125 was not immunohistochemically expressed in LMS tumors [27].
This study has some limitations. The analysis was performed on the basis of retrospective data, with the lack of detailed medical histories, short-term clinical outcomes, and detailed data on treatments after recurrence that could be related to prognosis. Because uterine LMS is a rare disease and analysis was performed with data from a single institution, the number of patients is smaller in this study than in other studies. A small number of cases may have caused an overfitting problem in multivariate analysis and may have reduced the accuracy of analysis. Race is known to be associated with differences in survival [14], but our study included patients who were almost all Asians. Despite the drawbacks of confounders and biases, we have drawn some valid conclusions from this limited data. This study suggests possible prognostic factors for not only RFS and OS but also survival after recurrence.
Further research should focus on the evaluation of patient counseling alternatives respect to these results. This information may be useful for counseling patients with uterine LMS. Also, research on developing improved technology to differentiate between benign and malignant uterine diseases should be performed to enable quicker surgical intervention for better prognosis. Additionally, the development of novel therapeutics for uterine LMS with poor prognosis is needed.
In conclusion, we demonstrated the possible prognostic factors for recurrence, OS, and survival after recurrence based on data from LMS patients treated at a single institution. Despite some limitations, these results provide useful information for patients with LMS.
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