Two versus three to four cycles of neoadjuvant immunochemotherapy for stage IB-IIIB non-small cell lung cancer: a real-world study.

IF 2.1 3区 医学 Q3 RESPIRATORY SYSTEM
Journal of thoracic disease Pub Date : 2025-02-28 Epub Date: 2025-02-27 DOI:10.21037/jtd-2024-2256
Yuhong Yang, Hang Zhao, Jiacong Liu, Xuhua Huang, Jiayue Ye, Jinming Xu, Wang Lv, Linhai Zhu, Jian Hu
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引用次数: 0

Abstract

Background: No consensus exists regarding the optimal number of cycles of neoadjuvant immunochemotherapy for patients with stage IB-IIIB non-small cell lung cancer (NSCLC). In this study, we compared the efficacy and safety of 2 cycles of neoadjuvant immunochemotherapy in stage IB-IIIB NSCLC with those of 3-4 cycles.

Methods: All patients with IB-IIIB NSCLC who received preoperative immunochemotherapy at the Department of Thoracic Surgery, the First Affiliated Hospital, Zhejiang University School of Medicine, from 2019 to 2022 were consecutively included in this retrospective study. Subsequently, 1:1 propensity score matching (PSM) according to baseline characteristics was performed to compare the efficacy and safety between the 2-cycle group and the 3 to 4-cycle group. The follow-up period was required to be at least 1 year after surgery or when the patient decided to abandon treatment.

Results: Of the 184 patients with stage IB-IIIB NSCLC included in the analysis, 61 received 2 cycles of neoadjuvant immunochemotherapy while 123 received 3-4 cycles. After a 1:1 PSM, there were no significant differences in baseline clinicopathological characteristics among the108 patients (54 pairs) who received 2 cycles or 3-4 cycles of neoadjuvant immunochemotherapy. The objective response rate (ORR) in the 3 to 4-cycle group was significantly higher than that in the 2-cycle group (83.3% vs. 63.0%; P=0.01). The incidence of grade 3-4 adverse events (AEs) in the 3 to 4-cycle group was similar to that of the 2-cycle group (13.0% vs. 9.3%; P=0.54). About 90.7% (49/54) of patients in the 2-cycle group and 46.3% (25/54) in the 3 to 4-cycle group eventually underwent surgery. The rate of major pathological response (MPR) in the 3 to 4-cycle group and 2-cycle group was 68.0% and 69.4% (P=0.90), respectively. The rate of pathological complete response (pCR) in the 3 to 4-cycle group and 2-cycle group was 36.0% and 38.8% (P=0.82), respectively. The median disease-free survival (DFS) in the 3 to 4-cycle group and 2-cycle group was not reached (P=0.80). The 1-year DFS rate and 2-year DFS rate in the 2-cycle group were 87.8% and 77.6%, respectively, while those in the 3 to 4-cycle group were 80.0% and 76.0%, respectively. The median overall survival (OS) in the 2-cycle group was 42.4 months, and it was not reached in the 3 to 4-cycle group (P=0.42). The 1-year OS rate and 2-year OS rate in the 2-cycle group were 93.9% and 87.8%, respectively, while those in the 3 to 4-cycle group were 88.0% and 80.0%, respectively.

Conclusions: Three to four cycles of neoadjuvant immunochemotherapy can result in more tumor regression in IB-IIIB NSCLC. Extending the number of cycles to 3-4 cycles may be feasible and safe in IB-IIIB NSCLC.

IB-IIIB期非小细胞肺癌的新辅助免疫化疗:一项现实世界的研究
背景:关于IB-IIIB期非小细胞肺癌(NSCLC)患者新辅助免疫化疗的最佳周期数,目前尚未达成共识。在这项研究中,我们比较了IB-IIIB期NSCLC患者新辅助免疫化疗2个周期与3-4个周期的疗效和安全性:方法:本回顾性研究连续纳入2019年至2022年在浙江大学医学院附属第一医院胸外科接受术前免疫化疗的所有IB-IIIB期NSCLC患者。随后,根据基线特征进行1:1倾向评分匹配(PSM),比较2周期组与3至4周期组的疗效和安全性。随访时间要求至少为术后1年或患者决定放弃治疗时:在184名IB-IIIB期NSCLC患者中,61人接受了2个周期的新辅助免疫化疗,123人接受了3-4个周期的新辅助免疫化疗。经过1:1 PSM后,接受2个周期或3-4个周期新辅助免疫化疗的108名患者(54对)的基线临床病理特征无显著差异。3至4周期组的客观反应率(ORR)明显高于2周期组(83.3%对63.0%;P=0.01)。3至4周期组的3-4级不良事件(AEs)发生率与2周期组相似(13.0% vs. 9.3%; P=0.54)。2周期组约90.7%(49/54)和3至4周期组约46.3%(25/54)的患者最终接受了手术。3至4周期组和2周期组的主要病理反应率(MPR)分别为68.0%和69.4%(P=0.90)。3至4周期组和2周期组的病理完全应答率(pCR)分别为36.0%和38.8%(P=0.82)。3至4周期组和2周期组的中位无病生存期(DFS)未达标(P=0.80)。2周期组的1年无病生存率和2年无病生存率分别为87.8%和77.6%,而3至4周期组分别为80.0%和76.0%。2周期组的中位总生存期(OS)为42.4个月,3至4周期组未达到这一目标(P=0.42)。2周期组的1年OS率和2年OS率分别为93.9%和87.8%,而3至4周期组分别为88.0%和80.0%:结论:新辅助免疫化疗3至4个周期可使IB-IIIB NSCLC患者的肿瘤消退更多。在IB-IIIB NSCLC中,将周期数延长至3-4个周期可能是可行且安全的。
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
Journal of thoracic disease
Journal of thoracic disease RESPIRATORY SYSTEM-
CiteScore
4.60
自引率
4.00%
发文量
254
期刊介绍: The Journal of Thoracic Disease (JTD, J Thorac Dis, pISSN: 2072-1439; eISSN: 2077-6624) was founded in Dec 2009, and indexed in PubMed in Dec 2011 and Science Citation Index SCI in Feb 2013. It is published quarterly (Dec 2009- Dec 2011), bimonthly (Jan 2012 - Dec 2013), monthly (Jan. 2014-) and openly distributed worldwide. JTD received its impact factor of 2.365 for the year 2016. JTD publishes manuscripts that describe new findings and provide current, practical information on the diagnosis and treatment of conditions related to thoracic disease. All the submission and reviewing are conducted electronically so that rapid review is assured.
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