Kim Ted, Hao Clara, Pan Minggui, Ganjoo Kristen N, Bui Nam Q
Division of Oncology, Department of Medicine, Stanford University, Stanford, CA 94305, USA.
Diseases. 2025 Mar 11;13(3):79. doi: 10.3390/diseases13030079.
BACKGROUND/OBJECTIVES: Locally advanced and metastatic leiomyosarcoma (LMS) is an aggressive cancer with limited treatment options. This single-institution, retrospective study evaluated the efficacy of first-line chemotherapy regimens in patients with advanced or metastatic LMS treated at Stanford Medical Center.
Seventy-four patients with unresectable or metastatic LMS were deemed eligible and treated with first-line chemotherapy regimens, including gemcitabine plus docetaxel, dacarbazine, doxorubicin combinations (with evofosfamide or ifosfamide), and doxorubicin monotherapy. Progression-free survival (PFS), overall survival (OS), and disease control rate (DCR) were assessed using RECIST v1.1, with survival analyses performed using Kaplan-Meier and Cox proportional hazards methods.
The cohort consisted of 56 females (75.7%) and 18 males (24.3%), with a median age of 55.5 years. The majority (93.2%) had metastatic disease. The median PFS for the entire cohort was 4.9 months (range: 0.6-28.1 mo), and the median OS was 27.3 months (range: 1.9-140.2 mo). The doxorubicin combination (DC) group had the highest median PFS of 7.9 months (range: 0.6-15.8 mo). Doxorubicin alone had the highest median OS of 33.8 months (4.2-100.2 mo). Doxorubicin combinations demonstrated superior PFS in both uterine and non-uterine LMS subgroups.
These findings reaffirm the efficacy of doxorubicin-based combination regimens as a first-line treatment for locally advanced and metastatic LMS, particularly in non-uterine LMS.
背景/目的:局部晚期和转移性平滑肌肉瘤(LMS)是一种侵袭性癌症,治疗选择有限。这项单机构回顾性研究评估了斯坦福医疗中心治疗的晚期或转移性LMS患者一线化疗方案的疗效。
74例不可切除或转移性LMS患者被认为符合条件并接受一线化疗方案治疗,包括吉西他滨加多西他赛、达卡巴嗪、阿霉素联合方案(与依沃福酰胺或异环磷酰胺联用)以及阿霉素单药治疗。采用RECIST v1.1评估无进展生存期(PFS)、总生存期(OS)和疾病控制率(DCR),使用Kaplan-Meier和Cox比例风险方法进行生存分析。
该队列包括56名女性(75.7%)和18名男性(24.3%),中位年龄为55.5岁。大多数(93.2%)患有转移性疾病。整个队列的中位PFS为4.9个月(范围:0.6 - 28.1个月),中位OS为27.3个月(范围:1.9 - 140.2个月)。阿霉素联合方案(DC)组的中位PFS最高,为7.9个月(范围:0.6 - 15.8个月)。单独使用阿霉素的中位OS最高,为33.8个月(4.2 - 100.2个月)。阿霉素联合方案在子宫和非子宫LMS亚组中均显示出更好的PFS。
这些发现再次证实了以阿霉素为基础的联合方案作为局部晚期和转移性LMS一线治疗的疗效,特别是在非子宫LMS中。