预防性颅照射对接受一线化学免疫治疗的大分期小细胞肺癌患者生存的影响:一项倾向评分匹配研究

IF 4.3 2区 医学 Q2 ONCOLOGY
Therapeutic Advances in Medical Oncology Pub Date : 2025-05-23 eCollection Date: 2025-01-01 DOI:10.1177/17588359251341158
Shichao Zhou, Wanchen Zhai, Qian Zhang, Hui Li, Yun Fan
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引用次数: 0

摘要

背景:化学免疫疗法已成为广泛期小细胞肺癌(ES-SCLC)的标准一线治疗方法,可改善生存结果。然而,预防性颅脑照射(PCI)在化学免疫治疗中的作用仍不明确。目的:本研究旨在评估PCI对ES-SCLC患者化疗免疫治疗后总生存率(OS)的影响。设计:回顾性研究。方法:回顾性分析2019年1月至2023年12月261例接受一线化学免疫治疗的ES-SCLC患者。所有患者都接受了核磁共振扫描,以确认没有脑转移。经1:2倾向评分匹配(PSM)后,分别将46例和81例患者分为PCI组和观察组。主要终点为OS,并进一步探索无进展生存期(PFS)、颅内转移的累积发生率和颅内无进展生存期(iPFS)。结果:经PSM治疗后,两组基线特征平衡良好。生存分析显示PCI组中位OS为19.9个月(95%可信区间(CI): 11.8 ~ 28.0),观察组中位OS为15.6个月(12.3 ~ 18.9),差异无统计学意义(风险比(HR) = 0.763 (95% CI: 0.484 ~ 1.206), log-rank p = 0.265)。PCI显著降低脑转移风险(Fine-Gray p = 0.002), PCI组1年累积发生率为13.8%(3.4% ~ 24.2%),观察组为53.4%(41.3% ~ 65.6%)。亚组分析显示,对于初始化学免疫治疗获得部分缓解的ES-SCLC患者,PCI组的中位生存期更长(25.7个月(95% CI: 15.4-36.1) vs 19.4个月(15.4-23.4);Hr = 0.502 (0.284 ~ 0.886);Log-rank p = 0.021)。结论:PCI并没有改善接受一线化疗免疫治疗的ES-SCLC患者的OS,但对于化疗免疫治疗后获得缓解的患者,PCI可能会提高生存期。此外,PCI可显著降低脑转移的发生率。这些发现需要进一步的随机研究来验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of prophylactic cranial irradiation on survival in extensive-stage small cell lung cancer receiving first-line chemoimmunotherapy: a propensity score-matched study.

Background: Chemoimmunotherapy has emerged as the standard first-line treatment for extensive-stage small cell lung cancer (ES-SCLC), improving survival outcomes. However, the role of prophylactic cranial irradiation (PCI) in the context of chemoimmunotherapy remains undefined.

Objectives: This study aimed to evaluate the impact of PCI on overall survival (OS) in patients with ES-SCLC after chemoimmunotherapy administration.

Design: Retrospective study.

Methods: This retrospective analysis included 261 patients with ES-SCLC treated with first-line chemoimmunotherapy between January 2019 and December 2023. All patients underwent MRI scans to confirm the absence of brain metastases. After 1:2 propensity score matching (PSM), 46 and 81 patients were assigned to the PCI and observation groups, respectively. The primary endpoint was OS, with additional exploration of progression-free survival (PFS), the cumulative incidence of intracranial metastases, and intracranial progression-free survival (iPFS).

Results: After PSM, the two groups were well-balanced in baseline characteristics. Survival analysis showed a median OS of 19.9 months (95% confidence interval (CI): 11.8-28.0) in the PCI group and 15.6 months (12.3-18.9) in the observation group, without a significant difference (hazard ratio (HR) = 0.763 (95% CI: 0.484-1.206), log-rank p = 0.265). PCI significantly reduced the risk of brain metastasis (Fine-Gray p = 0.002), with 1-year cumulative incidence rates of 13.8% (3.4%-24.2%) in the PCI group and 53.4% (41.3%-65.6%) in the observation group. Subgroup analysis showed that for ES-SCLC patients achieving a partial response to initial chemoimmunotherapy, the PCI group had longer median OS (25.7 months (95% CI: 15.4-36.1) vs 19.4 months (15.4-23.4); HR = 0.502 (0.284-0.886); log-rank p = 0.021).

Conclusion: PCI did not improve OS in ES-SCLC patients receiving first-line chemoimmunotherapy, while it may confer a survival benefit for patients who achieve remission following chemoimmunotherapy. In addition, PCI significantly reduced the incidence of brain metastases. These findings warrant further randomized studies for verification.

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来源期刊
CiteScore
8.20
自引率
2.00%
发文量
160
审稿时长
15 weeks
期刊介绍: Therapeutic Advances in Medical Oncology is an open access, peer-reviewed journal delivering the highest quality articles, reviews, and scholarly comment on pioneering efforts and innovative studies in the medical treatment of cancer. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers in medical oncology, providing a forum in print and online for publishing the highest quality articles in this area. This journal is a member of the Committee on Publication Ethics (COPE).
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