Neoadjuvant Chemoimmunotherapy for NSCLC

医学 化学免疫疗法 新辅助治疗 肿瘤科 化疗 内科学 癌症 乳腺癌 环磷酰胺
作者
Mark Sorin,Connor Prosty,Louis Ghaleb,Kathy Nie,Khaled Katergi,Muhammad H. Shahzad,Laurie-Rose Dubé,Aline Atallah,Anikka Swaby,Matthew Dankner,Trafford Crump,Logan A. Walsh,Pierre Fiset,Boris Sepesi,Patrick M. Forde,Tina Cascone,Mariano Provencio,Jonathan Spicer
出处
期刊:JAMA Oncology [American Medical Association]
卷期号:10 (5): 621-621 被引量:40
标识
DOI:10.1001/jamaoncol.2024.0057
摘要

Importance To date, no meta-analyses have comprehensively assessed the association of neoadjuvant chemoimmunotherapy with clinical outcomes in non–small cell lung cancer (NSCLC) in randomized and nonrandomized settings. In addition, there exists controversy concerning the efficacy of neoadjuvant chemoimmunotherapy for patients with NSCLC with programmed cell death 1 ligand 1 (PD-L1) levels less than 1%. Objective To compare neoadjuvant chemoimmunotherapy with chemotherapy by adverse events and surgical, pathological, and efficacy outcomes using recently published randomized clinical trials and nonrandomized trials. Data Sources MEDLINE and Embase were systematically searched from January 1, 2013, to October 25, 2023, for all clinical trials of neoadjuvant chemoimmunotherapy and chemotherapy that included at least 10 patients. Study Selection Observational studies and trials reporting the use of neoadjuvant radiotherapy, including chemoradiotherapy, molecular targeted therapy, or immunotherapy monotherapy, were excluded. Main Outcomes and Measures Surgical, pathological, and efficacy end points and adverse events were pooled using a random-effects meta-analysis. Results Among 43 eligible trials comprising 5431 patients (4020 males [74.0%]; median age range, 55-70 years), there were 8 randomized clinical trials with 3387 patients. For randomized clinical trials, pooled overall survival (hazard ratio, 0.65; 95% CI, 0.54-0.79; I 2 = 0%), event-free survival (hazard ratio, 0.59; 95% CI, 0.52-0.67; I 2 = 14.9%), major pathological response (risk ratio, 3.42; 95% CI, 2.83-4.15; I 2 = 31.2%), and complete pathological response (risk ratio, 5.52; 95% CI, 4.25-7.15; I 2 = 27.4%) favored neoadjuvant chemoimmunotherapy over neoadjuvant chemotherapy. For patients with baseline tumor PD-L1 levels less than 1%, there was a significant benefit in event-free survival for neoadjuvant chemoimmunotherapy compared with chemotherapy (hazard ratio, 0.74; 95% CI, 0.62-0.89; I 2 = 0%). Conclusion and Relevance This study found that neoadjuvant chemoimmunotherapy was superior to neoadjuvant chemotherapy across surgical, pathological, and efficacy outcomes. These findings suggest that patients with resectable NSCLC with tumor PD-L1 levels less than 1% may have an event-free survival benefit with neoadjuvant chemoimmunotherapy.
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