Li Haitian, Liu Qing, Li Bin, Chen Yuzhen, Lin Junping, Meng Yuqi, Feng Haiming, Zheng Zhizhong, Hui Yiming
Department of Thoracic Surgery, The Second Hospital & Clinical Medical School, Lanzhou University, Lanzhou 730030, China.
Zhongguo Fei Ai Za Zhi. 2024 Jun 20;27(6):421-430. doi: 10.3779/j.issn.1009-3419.2024.102.26.
Lung cancer is the cancer with the highest incidence and mortality rates in China, and non-small cell lung cancer (NSCLC) accounts for 80%-85% of all malignant lung tumors. Currently, surgical treatment remains the primary treatment modality for lung cancer. In recent years, the effectiveness of immune checkpoint inhibitors for NSCLC has become a consensus, and neoadjuvant immunochemotherapy (nICT) has shown promising efficacy and safety in early to intermediate stage NSCLC. However, there are fewer studies related to nICT for locally advanced NSCLC. This study aims to evaluate the efficacy and safety of nICT therapy in locally advanced resectable NSCLC.
85 confirmed resectable stage IIIA and IIIB patients treated in the Department of Thoracic Surgery, Second Hospital of Lanzhou University, from January 2021 to April 2024, were divided into the nICT group (n=32) and the surgery alone group (n=53). Clinical baseline data, perioperative indicators, postoperative complications, imaging response rate, pathological response rate, incidence of adverse events, and quality of life were compared between the two groups.
There were no statistically significant differences in clinical baseline data between the two groups (P>0.05). Incidence of choosing thoracotomy was higher in the nICT group than in the surgery alone group (P=0.002). There were no significant differences in surgical time, intraoperative blood loss, number of dissected lymph nodes, duration of chest tube placement, postoperative hospital stay, and R0 resection rate between the two groups (P>0.05). The overall incidence of postoperative complications was 31.25% in the nICT group and 22.64% in the surgery alone group, with no statistically significant difference (P=0.380). In the nICT group, the objective response rate (ORR) was 84.38%, with 5 cases of complete response (CR)(15.63%), 22 cases of partial response (PR)(68.75%), 15 cases of pathological response rate (pCR)(46.88%), and 11 cases of major pathological reaponse (MPR) (34.38%). During nICT treatment, 12 cases (37.50%) experienced grade 3 treatment-related adverse events, no death induced by adverse events or immune related adverse events. Moreover, the symptoms of the patients were improved after nICT treatment.
Neoadjuvant immunochemotherapy shows promising efficacy in locally advanced resectable NSCLC, with manageable treatment-related adverse events. It is a safe and feasible neoadjuvant treatment modality for locally advanced resectable NSCLC.
肺癌是中国发病率和死亡率最高的癌症,非小细胞肺癌(NSCLC)占所有恶性肺肿瘤的80%-85%。目前,手术治疗仍然是肺癌的主要治疗方式。近年来,免疫检查点抑制剂治疗NSCLC的有效性已成为共识,新辅助免疫化疗(nICT)在早期至中期NSCLC中显示出有前景的疗效和安全性。然而,关于局部晚期NSCLC的nICT研究较少。本研究旨在评估nICT治疗局部晚期可切除NSCLC的疗效和安全性。
选取2021年1月至2024年4月在兰州大学第二医院胸外科接受治疗的85例确诊为可切除的IIIA期和IIIB期患者,分为nICT组(n=32)和单纯手术组(n=53)。比较两组患者的临床基线数据、围手术期指标、术后并发症、影像缓解率、病理缓解率、不良事件发生率及生活质量。
两组患者临床基线数据差异无统计学意义(P>0.05)。nICT组开胸手术的发生率高于单纯手术组(P=0.002)。两组患者手术时间、术中出血量、清扫淋巴结数量、胸管留置时间、术后住院时间及R0切除率差异无统计学意义(P>0.05)。nICT组术后并发症总发生率为31.25%,单纯手术组为22.64%,差异无统计学意义(P=0.380)。nICT组客观缓解率(ORR)为84.38%,其中完全缓解(CR)5例(15.63%),部分缓解(PR)22例(68.75%),病理缓解率(pCR)15例(46.88%),主要病理缓解(MPR)11例(34.38%)。在nICT治疗期间,12例(37.50%)出现3级治疗相关不良事件,无不良事件或免疫相关不良事件导致的死亡。此外,nICT治疗后患者症状得到改善。
新辅助免疫化疗在局部晚期可切除NSCLC中显示出有前景的疗效,治疗相关不良事件可控。它是局部晚期可切除NSCLC一种安全可行的新辅助治疗方式。