Real-world effectiveness and safety of treatment strategies for unresectable, driver-negative Stage III NSCLC: A retrospective multicentre study.

IF 4.7 2区 医学 Q1 ONCOLOGY
Mingjun Xu, Yan Xu, Yingchun Man, Xuqin Xiang, Dexin Jia, Junzhu Dai, Weitong Gao, Ruqiong Wang, Bo An, Kaile Zhao, Jiaojiao Li, Bo Pan, Yan Yu
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引用次数: 0

Abstract

Concurrent or sequential chemoradiotherapy followed by immunotherapy (CCRT/SCRT→IO), known as the PACIFIC regimen, is the standard of care for unresectable, driver gene-negative Stage III non-small cell lung cancer (NSCLC). However, in real-world practice, some patients cannot proceed to immunotherapy due to toxicity, declining performance status, or disease progression. This multicenter retrospective study included 960 patients from 14 Chinese institutions (2011-2023) to evaluate the efficacy and safety of alternative regimens. Patients were stratified into five groups. Primary endpoints were progression-free survival (PFS) and overall survival (OS); secondary endpoints included objective response rate, disease control rate, duration of response, and immune-related adverse events (irAEs). Inverse probability treatment weighting was used to adjust for baseline differences. Among 911 evaluable patients, weighted median PFS was 21.7 months for (IO + CCRT/SCRT) → IO, 16.8 for (IO + Chemo) → IO, 25.8 for CCRT/SCRT → IO, 7.1 for chemotherapy alone, and 14.8 for CCRT/SCRT. Median OS was not reached in the (IO + CCRT/SCRT) → IO group and ranged from 31.1 to 58.3 months in others. No significant differences in PFS or OS were found between (IO + CCRT/SCRT) → IO and CCRT/SCRT → IO. Pneumonitis occurred most frequently in the CCRT/SCRT → IO group. Early initiation of IO did not significantly increase irAE risk. These findings support early integration of IO with chemoradiotherapy and maintenance IO as a viable option for unresectable Stage III NSCLC.

不可切除的驱动阴性III期NSCLC治疗策略的实际有效性和安全性:一项回顾性多中心研究
同步或顺序放化疗后免疫治疗(CCRT/SCRT→IO),被称为PACIFIC方案,是不可切除的驱动基因阴性III期非小细胞肺癌(NSCLC)的标准护理。然而,在现实世界的实践中,一些患者由于毒性、功能状态下降或疾病进展而无法进行免疫治疗。这项多中心回顾性研究纳入了来自中国14家机构的960例患者(2011-2023年),以评估替代方案的有效性和安全性。患者分为五组。主要终点为无进展生存期(PFS)和总生存期(OS);次要终点包括客观缓解率、疾病控制率、缓解持续时间和免疫相关不良事件(irAEs)。采用逆概率处理加权来调整基线差异。在911例可评估患者中,(IO + CCRT/SCRT)→IO组加权中位PFS为21.7个月,(IO + Chemo)→IO组为16.8个月,CCRT/SCRT→IO组为25.8个月,单独化疗组为7.1个月,CCRT/SCRT组为14.8个月。(IO + CCRT/SCRT)→IO组中位OS未达到,其他组中位OS为31.1 ~ 58.3个月。(IO + CCRT/SCRT)→IO与CCRT/SCRT→IO组PFS和OS无显著差异。肺炎在CCRT/SCRT→IO组发生率最高。早期开始IO治疗并没有显著增加irAE的风险。这些发现支持早期将IO与放化疗结合,维持IO作为不可切除的III期NSCLC的可行选择。
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
CiteScore
13.40
自引率
3.10%
发文量
460
审稿时长
2 months
期刊介绍: The International Journal of Cancer (IJC) is the official journal of the Union for International Cancer Control—UICC; it appears twice a month. IJC invites submission of manuscripts under a broad scope of topics relevant to experimental and clinical cancer research and publishes original Research Articles and Short Reports under the following categories: -Cancer Epidemiology- Cancer Genetics and Epigenetics- Infectious Causes of Cancer- Innovative Tools and Methods- Molecular Cancer Biology- Tumor Immunology and Microenvironment- Tumor Markers and Signatures- Cancer Therapy and Prevention
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