Sun Xiaoying, Roudi Raheleh, Chen Shangya, Fan Bin, Li Hong Jin, Zhou Min, Li Xin, Li Bin
Department of Dermatology, Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese Medicine Institute of Dermatology, Shanghai Academy of Traditional Chinese Medicine, Shanghai, China Oncopathology Research Center, Iran University of Medical Sciences, Tehran, Iran Department of Toxicology, Shandong Academy of Occupational Health and Occupational Medicine, Shandong academy of Medical Science, Jinan, Shandong, China.
Medicine (Baltimore). 2017 Nov;96(44):e8407. doi: 10.1097/MD.0000000000008407.
Nonsmall cell lung cancer accounts for approximately 80% of all lung cancers, and approximately 75% of cases are diagnosed in the middle and late stages of disease. Unfortunately, limited treatment does not improve the prognosis of advanced disease. Monoclonal antibodies targeting programmed cell death protein-1 (PD-1) and programmed death-ligand 1 (PD-L1) represent a new treatment paradigm for nonsmall cell lung cancer. Nevertheless, the immune-related adverse events (irAEs) associated with PD-1 and PD-L1 inhibitors are unique, and early recognition and treatment of these events are essential.
A systematic literature search will be performed using the EMBASE, MEDLINE, and Cochrane databases to identify relevant articles published in any language. Randomized clinical trials, case series, and case reports of PD-1 and PD-L1 inhibitors in the treatment of nonsmall cell lung cancer will be included. All meta-analyses will be performed using RevMan software. The quality of the studies will be evaluated using the guidelines listed in the Cochrane Handbook. If the necessary data are available, then subgroup analyses will be performed for high-, median-, and low-dose cohorts. The Preferred Reporting Items for Systematic Reviews and Meta-Analyses statements will be followed until the findings of the systematic review and meta-analysis are reported.
This will be the first systematic review and meta-analysis to describe previously reported irAEs related to PD-1 and PD-L1 inhibitors in the treatment of nonsmall cell lung cancer.
非小细胞肺癌约占所有肺癌的80%,约75%的病例在疾病的中晚期被诊断出来。不幸的是,有限的治疗并不能改善晚期疾病的预后。靶向程序性细胞死亡蛋白1(PD-1)和程序性死亡配体1(PD-L1)的单克隆抗体代表了非小细胞肺癌的一种新的治疗模式。然而,与PD-1和PD-L1抑制剂相关的免疫相关不良事件(irAE)是独特的,早期识别和治疗这些事件至关重要。
将使用EMBASE、MEDLINE和Cochrane数据库进行系统的文献检索,以识别以任何语言发表的相关文章。将纳入PD-1和PD-L1抑制剂治疗非小细胞肺癌的随机临床试验、病例系列和病例报告。所有的荟萃分析将使用RevMan软件进行。将根据Cochrane手册中列出的指南评估研究的质量。如果有必要的数据,将对高剂量、中剂量和低剂量队列进行亚组分析。在报告系统评价和荟萃分析的结果之前,将遵循系统评价和荟萃分析的首选报告项目声明。
这将是第一项系统评价和荟萃分析,描述先前报道的与PD-1和PD-L1抑制剂治疗非小细胞肺癌相关的irAE。