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非小细胞肺癌中的新辅助免疫检查点抑制剂

Neoadjuvant Immune Checkpoint Inhibitors in Non-small Cell Lung Cancer.

作者信息

Xue Chongxiang, Dong Huijing, Chen Ying, Lu Xingyu, Zheng Shuyue, Cui Huijuan

机构信息

Beijing University of Chinese Medicine, Beijing, China.

Department of Clinical Oncology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.

出版信息

J Coll Physicians Surg Pak. 2022 Jun;32(6):779-788. doi: 10.29271/jcpsp.2022.06.779.

Abstract

Lung cancer is the leading cause of cancer-related death worldwide. A meta-analysis was conducted to assess the benefits and risks of neoadjuvant immune checkpoint inhibitors (ICIs) in non-small cell lung cancer (NSCLC). Online databases, including PubMed, Embase, Web of Science, Cochrane Library, and clinicaltrials.gov, were retrospectively and systematically searched for eligible trials from database inception to May 2021. A total of 792 patients from 21 clinical trials were included. For surgical data, the pooled operation rate and R0 resection rate were 92% (95% CI 87-96%) and 97% (95% CI 94-99%). Additionally, neoadjuvant ICIs achieved a major pathological response (MPR) of 39% (95% CI 25-53%), including 25% (95% CI 16-36%) pathological complete response (pCR). With radiological response assessment, the pooled objective response rate (ORR) and disease control rate (DCR) were 44% (95% CI 21-68%) and 88% (95% CI 75-98%), respectively. In terms of safety, the pooled rate of any-grade and grade 3-5 treatment-related adverse effects (TRAEs) were 57% (95% CI 38-76%) and 15% (95% CI 6-28%). Eventually, the study concludes that neoadjuvant ICIs are effective and safe for patients with early-stage NSCLC. Key Words: Neoadjuvant therapy, Immune checkpoint inhibitors, Non-small cell lung cancer, Meta-analysis.

摘要

肺癌是全球癌症相关死亡的主要原因。进行了一项荟萃分析,以评估新辅助免疫检查点抑制剂(ICI)在非小细胞肺癌(NSCLC)中的益处和风险。对包括PubMed、Embase、Web of Science、Cochrane图书馆和clinicaltrials.gov在内的在线数据库进行回顾性和系统性检索,以查找从数据库建立至2021年5月的符合条件的试验。共纳入了来自21项临床试验的792例患者。关于手术数据,汇总的手术率和R0切除率分别为92%(95%CI 87-96%)和97%(95%CI 94-99%)。此外,新辅助ICI实现了39%(95%CI 25-53%)的主要病理缓解(MPR),包括25%(95%CI 16-36%)的病理完全缓解(pCR)。通过放射学反应评估,汇总的客观缓解率(ORR)和疾病控制率(DCR)分别为44%(95%CI 21-68%)和88%(95%CI 75-98%)。在安全性方面,任何级别和3-5级治疗相关不良反应(TRAE)的汇总发生率分别为57%(95%CI 38-76%)和15%(95%CI 6-28%)。最终,该研究得出结论,新辅助ICI对早期NSCLC患者有效且安全。关键词:新辅助治疗;免疫检查点抑制剂;非小细胞肺癌;荟萃分析。

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