Shichao Zhou, Wanchen Zhai, Qian Zhang, Hui Li, Yun Fan
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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).</p><p><strong>Results: </strong>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 <i>p</i> = 0.265). PCI significantly reduced the risk of brain metastasis (Fine-Gray <i>p</i> = 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 <i>p</i> = 0.021).</p><p><strong>Conclusion: </strong>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.</p>","PeriodicalId":23053,"journal":{"name":"Therapeutic Advances in Medical Oncology","volume":"17 ","pages":"17588359251341158"},"PeriodicalIF":4.3000,"publicationDate":"2025-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12102569/pdf/","citationCount":"0","resultStr":"{\"title\":\"Impact of prophylactic cranial irradiation on survival in extensive-stage small cell lung cancer receiving first-line chemoimmunotherapy: a propensity score-matched study.\",\"authors\":\"Shichao Zhou, Wanchen Zhai, Qian Zhang, Hui Li, Yun Fan\",\"doi\":\"10.1177/17588359251341158\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>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.</p><p><strong>Objectives: </strong>This study aimed to evaluate the impact of PCI on overall survival (OS) in patients with ES-SCLC after chemoimmunotherapy administration.</p><p><strong>Design: </strong>Retrospective study.</p><p><strong>Methods: </strong>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).</p><p><strong>Results: </strong>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 <i>p</i> = 0.265). PCI significantly reduced the risk of brain metastasis (Fine-Gray <i>p</i> = 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 <i>p</i> = 0.021).</p><p><strong>Conclusion: </strong>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. 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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。
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.
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).