基于免疫治疗方案或化疗的晚期肺肉瘤样癌患者临床结果的比较:一项基于SEER数据库和多中心现实环境的研究

Duanyang Peng, Le Xiong, Yuxi Luo, Junxing Chen, Yue'e Zheng, Xiaoli Zeng, Shubin Liu, Anwen Liu, Xia Wang, Zhimin Zeng
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引用次数: 0

摘要

背景:肺肉瘤样癌(Pulmonary sarcomatoid carcinoma, PSC)是一种以早期转移和侵袭为特征的罕见肺癌。它主要诊断在局部晚期或转移阶段,阻碍了手术干预的可能性。然而,晚期PSC的标准治疗方法尚未建立。本研究评估了化疗和基于免疫治疗的策略在晚期PSC患者中的作用。方法:这项回顾性研究使用了监测、流行病学和最终结果(SEER)数据库和来自三个癌症中心的数据。使用Kaplan-Meier法估计无进展生存期(PFS)和总生存期(OS)。进行单因素和多因素分析以确定预后因素。结果:从SEER数据库中共发现202例IV期PSC患者(中位生存期,5个月)。三个中心患者的中位随访时间为18.8个月。分别对12名和27名患者进行一线免疫治疗和化疗。中位PFS分别为2.1和7.3个月[风险比(HR), 0.16;95%置信区间(CI), 0.06-0.40;P < 0.001],而中位OS分别为3.6和21.4个月(HR, 0.21;95% ci, 0.09-0.50;P < 0.001),分别为化疗组和免疫组。以免疫治疗为基础的方案是PFS的独立预后因素(HR, 0.21;95% ci, 0.08-0.55;P = 0.001)和OS (HR, 0.20;95% ci, 0.08-0.49;P < 0.001)。结论:常规化疗对晚期PSC患者的疗效有限;然而,那些接受一线免疫治疗方案的患者表现出明显改善的反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison of clinical outcomes in patients with advanced pulmonary sarcomatoid carcinoma treated with immunotherapy-based regimens or chemotherapy: A study based on the SEER database and multicentric real-world settings.

Background: Pulmonary sarcomatoid carcinoma (PSC) is a rare lung cancer characterized by early metastasis and invasion. It is predominantly diagnosed at a locally advanced or metastatic stage, hindering the possibility of surgical intervention. However, a standard treatment for advanced PSC remains unestablished. This study evaluated the effects of chemotherapy and immunotherapy-based strategies in patients with advanced PSC.

Methods: The Surveillance, Epidemiology, and End Results (SEER) database and data from three cancer centers were used in this retrospective study. Progression-free survival (PFS) and overall survival (OS) were estimated using the Kaplan-Meier method. Univariate and multivariate analyses were conducted to identify the prognostic factors.

Results: In total, 202 patients with stage IV PSC were identified from the SEER database (median OS, 5 months). The median follow-up time of patients from the three centers was 18.8 months. First-line treatment with immunotherapy-based regimens and chemotherapy was administered to 12 and 27 patients, respectively. The median PFS was 2.1 and 7.3 months [hazard ratio (HR), 0.16; 95% confidence interval (CI), 0.06-0.40; P < 0.001], while the median OS was 3.6 and 21.4 months (HR, 0.21; 95% CI, 0.09-0.50; P < 0.001) in the chemotherapy and immune-based groups, respectively. The immunotherapy-based regimen was an independent prognostic factor for PFS (HR, 0.21; 95% CI, 0.08-0.55; P = 0.001) and OS (HR, 0.20; 95% CI, 0.08-0.49; P < 0.001).

Conclusions: Conventional chemotherapy offered limited benefits in patients with advanced PSC; however, those who received first-line immunotherapy-based regimens exhibited significantly improved responses.

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