Lamm Wolfgang, Natter Camilla, Schur Sophie, Köstler Wolfgang J, Reinthaller Alexander, Krainer Michael, Grimm Christoph, Horvath Reinhard, Amann Gabriele, Funovics Philipp, Brodowicz Thomas, Polterauer Stephan
Department of Gynecology and Gynecologic Oncology, Medical University of Vienna, 18-20 Waehringer Guertel, 1090 Vienna, Austria.
BMC Cancer. 2014 Dec 18;14:981. doi: 10.1186/1471-2407-14-981.
Leiomyosarcomas represent the largest subtype of soft tissue sarcomas. Two subgroups can be distinguished, non-uterine (NULMS) and uterine leiomyosarcomas (ULMS). The aim of this retrospective study was to evaluate differences in clinical features and outcome between these two subgroups.
Outcome and clinical-pathological parameters between 50 patients with NULMS and 45 patients with ULMS were assessed, and compared between both groups. Univariate and multivariable survival analyses were performed.
Patients with ULMS presented with larger tumors when compared to patients with NULMS (p < 0.001). More patients with ULMS initially presented with metastatic disease (67% vs. 36%, p = 0.007). Most common metastatic site was lung for both subtypes (28% and 38%). Five-year overall survival (OS) rates of 82.6% and 41.2% and median OS times of 92.6 (range: 79.7-105.4) and 50.4 (range: 34.8-66.0) months were observed in patients with NULMS and ULMS, respectively (p = 0.006). In multivariate analysis, initial metastatic disease remained an independent prognostic factor in terms of OS (p < 0.0001).
At time of diagnosis ULMS were larger and more often metastasized. Therefore patients with ULMS showed unfavorable outcome when compared to NULMS. Later diagnosis might be caused by differences in symptoms and clinical presentation or a more aggressive biological tumor behavior.
平滑肌肉瘤是软组织肉瘤中最大的亚型。可分为两个亚组,即非子宫平滑肌肉瘤(NULMS)和子宫平滑肌肉瘤(ULMS)。本回顾性研究的目的是评估这两个亚组在临床特征和预后方面的差异。
评估了50例NULMS患者和45例ULMS患者的预后及临床病理参数,并在两组之间进行比较。进行了单因素和多因素生存分析。
与NULMS患者相比,ULMS患者的肿瘤更大(p < 0.001)。更多的ULMS患者最初表现为转移性疾病(67%对36%,p = 0.007)。两种亚型最常见的转移部位均为肺(分别为28%和38%)。NULMS和ULMS患者的5年总生存率(OS)分别为82.6%和41.2%,中位OS时间分别为92.6(范围:79.7 - 105.4)和50.4(范围:34.8 - 66.0)个月(p = 0.006)。在多因素分析中,初始转移性疾病在OS方面仍然是一个独立的预后因素(p < 0.0001)。
在诊断时,ULMS更大且更常发生转移。因此,与NULMS相比,ULMS患者的预后较差。诊断较晚可能是由于症状和临床表现的差异或肿瘤更具侵袭性的生物学行为所致。