The outcome of advanced and recurrent cervical cancer patients treated with first-line platinum and paclitaxel with or without indication for immune checkpoint inhibitors: the comparative study.

IF 3.4 2区 医学 Q2 ONCOLOGY BMC Cancer Pub Date : 2024-10-11 DOI:10.1186/s12885-024-12989-x
Lan Feng, Qun Shi, Shujuan Wang, Ye Zhao, Haiyan Wu, Lei Wei, Qing Hao, Zhaojun Cui, Lin Wang, Jing Zhang, Dan Zhang, Xinxin Zhan, Jingwen Jiang
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Abstract

Objective: Immune checkpoint inhibitor (ICI) therapy activates the immune system to recognize and eliminate cancer cells that have escaped surveillance. This study aimed to compare the treatment outcome of advanced and recurrent cervical cancer patients treated with first-line platinum and paclitaxel with or without ICI.

Methods: Data from 69 advanced and recurrent cervical cancer patients treated with first-line ICI plus platinum and paclitaxel (N = 33) or first-line platinum and paclitaxel (N = 36) were reviewed between March 2020 and January 2023 in this retrospective study. Patients chose treatment based on the actual disease condition, patient willingness, and medical advice. Additionally, objective response rate (ORR), disease control rate (DCR), progression-free survival (PFS), and overall survival (OS) were calculated, and adverse events were gained.

Results: There was no difference in baseline data between patients receiving the two different treatments (all P > 0.05). Complete response rate (18.2% vs. 8.3%; P = 0.294), ORR (48.5% vs. 30.6%; P = 0.127), and DCR (81.8% vs. 72.2%; P = 0.345) tended to ascend in patients treated with ICI plus platinum and paclitaxel compared to those treated with platinum and paclitaxel, although there was no statistical significance. In patients treated with ICI plus platinum and paclitaxel, the median PFS was 10.3 months and the median OS was not reached. Meanwhile, the median PFS and OS were 7.7 and 16.9 months in patients treated with platinum and paclitaxel. PFS (P = 0.036) and OS (P = 0.033) were increased in patients treated with ICI plus platinum and paclitaxel versus those treated with platinum and paclitaxel, which was verified by multivariate Cox regression analyses (both P < 0.05). No difference was observed in the occurrence of adverse events between patients receiving the two different treatments (all P > 0.05).

Conclusion: First-line ICI plus platinum and paclitaxel yields better treatment responses, longer survival, and non-differential adverse events versus first-line platinum and paclitaxel in advanced and recurrent cervical cancer patients.

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接受一线铂类和紫杉醇治疗的晚期和复发性宫颈癌患者使用或不使用免疫检查点抑制剂的疗效比较研究。
目的:免疫检查点抑制剂(ICI)疗法可激活免疫系统,识别并消除逃避监控的癌细胞。本研究旨在比较接受一线铂类和紫杉醇治疗的晚期和复发性宫颈癌患者接受 ICI 或不接受 ICI 治疗的疗效:在这项回顾性研究中,回顾了2020年3月至2023年1月期间接受一线ICI加铂类和紫杉醇(33例)或一线铂类和紫杉醇(36例)治疗的69例晚期和复发性宫颈癌患者的数据。患者根据实际病情、患者意愿和医嘱选择治疗方法。此外,还计算了客观反应率(ORR)、疾病控制率(DCR)、无进展生存期(PFS)和总生存期(OS),并获得了不良事件:结果:接受两种不同治疗方法的患者在基线数据上没有差异(P>0.05)。与接受铂类和紫杉醇治疗的患者相比,接受ICI加铂类和紫杉醇治疗的患者的完全反应率(18.2% vs. 8.3%;P = 0.294)、ORR(48.5% vs. 30.6%;P = 0.127)和DCR(81.8% vs. 72.2%;P = 0.345)呈上升趋势,但无统计学意义。在接受 ICI 加铂和紫杉醇治疗的患者中,中位 PFS 为 10.3 个月,中位 OS 未达到。与此同时,接受铂和紫杉醇治疗的患者的中位 PFS 和 OS 分别为 7.7 个月和 16.9 个月。ICI联合铂类和紫杉醇治疗患者的PFS(P = 0.036)和OS(P = 0.033)较铂类和紫杉醇治疗患者有所增加,多变量Cox回归分析证实了这一点(均为P 0.05):结论:在晚期和复发性宫颈癌患者中,一线 ICI 加铂和紫杉醇与一线铂和紫杉醇相比,可获得更好的治疗反应、更长的生存期和无差异的不良反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Cancer
BMC Cancer 医学-肿瘤学
CiteScore
6.00
自引率
2.60%
发文量
1204
审稿时长
6.8 months
期刊介绍: BMC Cancer is an open access, peer-reviewed journal that considers articles on all aspects of cancer research, including the pathophysiology, prevention, diagnosis and treatment of cancers. The journal welcomes submissions concerning molecular and cellular biology, genetics, epidemiology, and clinical trials.
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