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程序性细胞死亡配体 1 表达与早期非小细胞肺癌患者切除术后临床结局的相关性:一项真实世界研究。

Programmed Cell Death-Ligand 1 Expression and Clinical Outcomes Among Patients with Resected, Early-Stage Non-Small Cell Lung Cancer: A Real-World Study.

机构信息

William Osler Health System, University of Toronto, 2100 Bovaird Drive, Brampton, ON L6R 3J7, Canada.

Department of Medicine, University of Toronto, 27 King's College Circle, Toronto, ON M5S 1A1, Canada.

出版信息

Curr Oncol. 2024 Oct 31;31(11):6735-6748. doi: 10.3390/curroncol31110497.

DOI:10.3390/curroncol31110497
PMID:39590128
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11593080/
Abstract

Treatment options for non-small cell lung cancer (NSCLC) are evolving, given recent and expected approvals of immune checkpoint inhibitors (ICIs) targeting programmed cell death-(ligand) 1 (PD-1/PD-L1). We retrospectively evaluated outcomes among patients with resected stage IB-IIIA NSCLC tumors expressing PD-L1 using PALEOS (Pan-cAnadian Lung cancEr Observational Study) data (2016-2019). Key outcomes included PD-L1 expression rate and treatment patterns, recurrence, and median overall (mOS) and disease-free survival (mDFS) among PD-L1+ patients. Among 539 PD-L1-tested patients, 317 (58.8%) were PD-L1+ (≥1%). At diagnosis, 35.3%, 39.8%, and 24.9% of PD-L1+ patients had stage IB, II, or IIIA disease. Forty-one percent had received adjuvant therapy. At 22.6 months (median follow-up), first disease recurrence had occurred in 31.9% of patients, primarily at metastatic sites. After first metastatic recurrence, ICI regimens were the most common first systemic therapy (29.8%). mOS was not reached; mDFS was 40.0 months. At four years, DFS probability was 44%. Four-year OS and DFS rates were generally similar when stratified by PD-L1 expression (1-49% vs. ≥50%). These findings underscore the generally poor outcomes experienced by patients with early-stage, resected, PD-L1+ NSCLC after treatment with available adjuvant therapies, and provide context to recent and emerging trials of new treatment options.

摘要

治疗选择非小细胞肺癌 (NSCLC) 正在发展,鉴于最近和预期批准的免疫检查点抑制剂 (ICI) 针对程序性细胞死亡-(配体) 1 (PD-1/PD-L1)。我们回顾性评估了使用 PALEOS(泛加拿大肺癌观察性研究)数据 (2016-2019 年) 表达 PD-L1 的可切除 IB-IIIA 期 NSCLC 肿瘤患者的结果。主要结果包括 PD-L1 表达率和治疗模式、复发以及 PD-L1+患者的中位总生存期 (mOS) 和无病生存期 (mDFS)。在 539 名 PD-L1 检测患者中,317 名 (58.8%) 为 PD-L1+ (≥1%)。在诊断时,35.3%、39.8%和 24.9%的 PD-L1+患者患有 IB、II 或 IIIA 期疾病。41%接受了辅助治疗。在 22.6 个月(中位随访)时,31.9%的患者首次出现疾病复发,主要发生在转移性部位。在首次转移性复发后,ICI 方案是最常见的一线全身治疗方案 (29.8%)。mOS 未达到;mDFS 为 40.0 个月。四年时,DFS 概率为 44%。按 PD-L1 表达分层 (1-49% vs. ≥50%),四年 OS 和 DFS 率大致相似。这些发现强调了接受现有辅助治疗的早期、可切除、PD-L1+ NSCLC 患者的总体预后较差,并为最近和新兴的新治疗选择试验提供了背景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/077a/11593080/3a9911f5c450/curroncol-31-00497-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/077a/11593080/aac96992ea92/curroncol-31-00497-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/077a/11593080/3a9911f5c450/curroncol-31-00497-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/077a/11593080/aac96992ea92/curroncol-31-00497-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/077a/11593080/3a9911f5c450/curroncol-31-00497-g002.jpg

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