Department of Medical Oncology, Tepecik Training and Research Hospital, 35180 Izmir, Türkiye.
Department of Oncology, Hacettepe University Cancer Institute, 06410 Ankara, Türkiye.
Curr Oncol. 2024 Nov 1;31(11):6803-6813. doi: 10.3390/curroncol31110502.
(1) Background: Metastatic L-type sarcomas (liposarcoma and leiomyosarcoma) are rare and have a poor prognosis. Trabectedin is an effective agent that can be used after anthracyclines. This study was designed to evaluate the real-life effectiveness and safety of trabectedin. (2) Methods: A retrospective multicenter study was conducted on patients who were treated with trabectedin for metastatic L-type sarcomas at ten tertiary oncology centers between 2015 and 2023. The objective response rate (ORR), disease control rate (DCR), time to treatment failure (TTF), and overall survival (OS) were evaluated in the cohort. Cox regression analysis was used to determine prognostic factors for survival. (3) Results: A total of 98 patients (52% liposarcoma and 48% leiomyosarcoma) were included in the study. The median treatment line was three (range: 1 to 6). Thirteen patients (13.3%) underwent local treatment due to oligoprogression, and dose reduction was required in seventeen patients (17.3%) due to toxicity. The ORR and DCR were 16% and 42%, respectively. The median TTF was 3 months, and the median OS was 10 months. In univariate analysis, a significantly longer median TTF was observed in patients who underwent local treatment ( = 0.008), obtained objective responses ( < 0.001), and underwent dose reduction ( = 0.002). No statistical differences were observed according to the histologic subtype and metastatic site. In the multivariate analysis for OS, it was found that obtaining an objective response was a good prognostic factor ( = 0.003), while the presence of liver metastases was associated with a poor prognosis ( = 0.016). (4) Conclusion: Trabectedin is a suitable option for L-type sarcoma after doxorubicin-based treatments. Survival was not worse in patients who underwent dose reduction. The use of local therapies simultaneously with trabectedin can be effective.
(1) 背景:转移性 L 型肉瘤(脂肪肉瘤和 leiomyosarcoma)罕见且预后不良。Trabectedin 是一种有效的药物,可在蒽环类药物后使用。本研究旨在评估 trabectedin 的真实疗效和安全性。
(2) 方法:对 2015 年至 2023 年期间,十家三级肿瘤中心的 98 例转移性 L 型肉瘤患者接受 trabectedin 治疗进行回顾性多中心研究。在该队列中评估了客观缓解率(ORR)、疾病控制率(DCR)、治疗失败时间(TTF)和总生存期(OS)。Cox 回归分析用于确定生存的预后因素。
(3) 结果:共纳入 98 例患者(52%脂肪肉瘤和 48% leiomyosarcoma)。中位治疗线数为 3 条(范围:1-6 条)。13 例患者(13.3%)因寡进展而接受局部治疗,17 例患者(17.3%)因毒性而需要减少剂量。ORR 和 DCR 分别为 16%和 42%。中位 TTF 为 3 个月,中位 OS 为 10 个月。单因素分析显示,局部治疗( = 0.008)、获得客观缓解( < 0.001)和剂量减少( = 0.002)的患者中位 TTF 显著延长。根据组织学亚型和转移部位,未观察到统计学差异。OS 的多因素分析发现,获得客观缓解是一个良好的预后因素( = 0.003),而存在肝转移与预后不良相关( = 0.016)。
(4) 结论:Trabectedin 是蒽环类药物治疗后 L 型肉瘤的一种合适选择。剂量减少的患者生存情况并不差。同时使用局部治疗与 trabectedin 可能是有效的。