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免疫检查点抑制剂在非小细胞肺癌新辅助治疗中的应用:一项系统评价和荟萃分析。

Immune checkpoint inhibitors in neoadjuvant therapy of non-small cell lung cancer: a systematic review and meta-analysis.

作者信息

Ge Sa, Huang Chenjun

机构信息

The First Clinical Medical College of Nanjing Medical University, Nanjing, China.

Department of Thoracic Surgery, Jiangsu Province Hospital and The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.

出版信息

J Thorac Dis. 2022 Feb;14(2):333-342. doi: 10.21037/jtd-21-1664.

Abstract

BACKGROUND

Our objective was to explore the safety and feasibility of immune checkpoint inhibitors (ICIs) in the neoadjuvant treatment of non-small cell lung cancer (NSCLC).

METHODS

Embase, PubMed and Web of Science were systematically searched from 1 January 2018 to 1 August 2021 for studies with data on the treatment-related adverse reactions (TRAE), immune-related adverse events (irAE), perioperative information, major pathological response (MPR), pathologic complete remission (pCR) and objective response rate (ORR). The QUADAS-2 tool was used to assess the quality of the studies, then the data were transformed for meta-analysis. Review Manager 5.3 (Cochrane) was used for statistical analyses with a P value of <0.05 considered significant.

RESULTS

Thirteen studies with 358 patients were included in this meta-analysis, of which, 218 patients received ICI and chemotherapy-containing regimens and 140 patients received neoadjuvant ICIs only. The 157 (72.0%) patients who received combined neoadjuvant therapy showed a higher incidence of TRAEs, while only 37 (26.4%) patients who received neoadjuvant ICIs experienced TRAEs. Grade 3 or higher irAEs were observed in 92 (25.7%) patients, of which, 81 patients belonged to the neoadjuvant immunochemotherapy subgroup. The surgical resection rate was between 38.5-100%, with only two patients experiencing a delay in surgery. Complication rates were between 3.6-100% in the 8 studies that reported postoperative complications, with more postoperative complications [35 (18.9%)] identified in the neoadjuvant immunochemotherapy subgroup. Of which 176 patients achieved MPR, 126 received ICI and chemotherapy combined neoadjuvant therapy. Seventy-one of 95 patients who had achieved pCR had undergone ICI and chemotherapy. Compared with the neoadjuvant immunotherapy group, patients undergoing ICI and chemotherapy achieved more radiological response [118 (54.1%)] than patients undergoing ICIs [25 (17.9%)] only. The odds ratio (OR) value of the MPR/pCR/ORR rate in the neoadjuvant immunochemotherapy group was higher [OR =0.55/0.32/0.39, 95% confidence interval (CI): 0.44-0.66/0.22-0.44/0.26-0.53, P=0.0004/0.14/<0.0001] after transformation.

DISCUSSION

Neoadjuvant immunotherapy shows lower toxicity and fewer perioperative complications. ICI combined chemotherapy can achieve more pathological relief and clinical benefits in the neoadjuvant treatment of NSCLC but is associated with increased irAE and perioperative complications. However, the small sample size limits the reliability of the research.

摘要

背景

我们的目的是探讨免疫检查点抑制剂(ICI)在非小细胞肺癌(NSCLC)新辅助治疗中的安全性和可行性。

方法

系统检索Embase、PubMed和Web of Science数据库,检索时间为2018年1月1日至2021年8月1日,纳入有关治疗相关不良反应(TRAE)、免疫相关不良事件(irAE)、围手术期信息、主要病理缓解(MPR)、病理完全缓解(pCR)和客观缓解率(ORR)数据的研究。使用QUADAS - 2工具评估研究质量,然后对数据进行转换以进行荟萃分析。采用Review Manager 5.3(Cochrane)进行统计分析,P值<0.05被认为具有统计学意义。

结果

本荟萃分析纳入了13项研究共358例患者,其中218例患者接受了ICI与含化疗方案,140例患者仅接受新辅助ICI治疗。接受新辅助联合治疗的157例(72.0%)患者TRAE发生率较高,而仅接受新辅助ICI治疗的患者中只有37例(26.4%)发生TRAE。92例(25.7%)患者观察到3级或更高等级的irAE,其中81例患者属于新辅助免疫化疗亚组。手术切除率在38.5% - 100%之间,只有2例患者手术延迟。在报告术后并发症的8项研究中,并发症发生率在3.6% - 100%之间,新辅助免疫化疗亚组中术后并发症更多[35例(18.9%)]。其中176例患者实现了MPR,126例接受了ICI与化疗联合新辅助治疗。95例实现pCR的患者中有71例接受了ICI与化疗。与新辅助免疫治疗组相比,接受ICI与化疗的患者比仅接受ICI治疗的患者获得更多的影像学缓解[118例(54.1%)对25例(17.9%)]。新辅助免疫化疗组MPR/pCR/ORR率的比值比(OR)值更高[OR =0.55/0.32/0.39,95%置信区间(CI):0.44 - 0.66/0.22 - 0.44/0.26 - 0.53,P =0.0004/0.14/<0.0001],转换后数据如此。

讨论

新辅助免疫治疗显示出较低的毒性和较少的围手术期并发症。ICI联合化疗在NSCLC新辅助治疗中可实现更多的病理缓解和临床获益,但与irAE增加和围手术期并发症相关。然而,样本量较小限制了研究的可靠性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/970f/8902100/b65902852934/jtd-14-02-333-f1.jpg

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