中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
PD-1 inhibitor combined with apatinib for advanced gastric or esophagogastric junction cancer: a retrospective study

文献类型:期刊论文

作者Wei, Qing1,2; Yuan, Xing1,2; Li, Jingjing1,2; Xu, Qi1,2; Ying, Jieer1,2
刊名TRANSLATIONAL CANCER RESEARCH
出版日期2020-09-01
卷号9
关键词Programmed death 1 (PD-1) gastric cancer (GC) immune checkpoint inhibitors immunotherapy apatinib
ISSN号2218-676X
DOI10.21037/tcr-20-1333
通讯作者Xu, Qi(hzxuqi@sina.cn) ; Ying, Jieer(jieerying@aliyun.com)
英文摘要Background: Nivolumab and pembrolizumab were approved as immune checkpoint inhibitors for third-line treatment of advanced gastric or esophagogastric junction cancer (GC/EGJC) in 2017. However, immunotherapy monotherapy has low efficacy. Apatinib has been proven effective in advanced GC/EGJC. Numerous studies have shown that immunotherapy has a synergistic effect when combined with targeted drug therapy. Based on these facts and to assess the efficacy and safety of programmed death 1 (PD-1) inhibitor and apatinib as combination therapy in patients (pts) with unresectable locally advanced or metastatic GC/EGJC, a retrospective clinical research study was carried out. Methods: Pts (n=24) received PD-1 inhibitor and apatinib (250 mg once daily) as second- or third-line therapy in this observational, retrospective study. The primary objectives were efficacy and safety. Results: At data cut-off (December 31, 2019), 24 pts were enrolled. Of the 19 pts who were evaluable, the objective response rate (ORR) was 26.3% (5/19), the median progression-free survival (PFS) was 3.0 (95% CI: 1.3 to 4.7) months, and the median overall survival (OS) was not reached. Grade 3 or 4 treatment-related adverse events (TRAEs) occurred in 3 (15.8%) of the 19 pts. These adverse events (AEs) included pruritus, rash, hand-foot syndrome, and increased aspartate aminotransferase (AST) or alanine aminotransferase (ALT). No treatment-related deaths occurred. Conclusions: Combination therapy of PD-1 inhibitor and apatinib showed encouraging clinical activity and demonstrated tolerable toxicity in pts with advanced GC/EGJC. Hence, our work provide rationale for the combination of PD-1 inhibitor and apatinib in advanced GC/EGJC.
WOS关键词TUMOR MICROENVIRONMENT ; DOUBLE-BLIND ; IMMUNOTHERAPY ; CHEMOTHERAPY ; VASCULATURE ; THERAPIES ; BLOCKADE
资助项目Zhejiang Chinese Medicine Science and Technology Program[2018ZB022]
WOS研究方向Oncology
语种英语
WOS记录号WOS:000575123400020
出版者AME PUBL CO
资助机构Zhejiang Chinese Medicine Science and Technology Program
源URL[http://ir.hfcas.ac.cn:8080/handle/334002/104299]  
专题中国科学院合肥物质科学研究院
通讯作者Xu, Qi; Ying, Jieer
作者单位1.Univ Chinese Acad Sci, Zhejiang Canc Hosp, Canc Hosp, Dept Abdominal Med Oncol, Hangzhou, Peoples R China
2.Chinese Acad Sci, Inst Canc & Basic Med ICBM, Hangzhou, Peoples R China
推荐引用方式
GB/T 7714
Wei, Qing,Yuan, Xing,Li, Jingjing,et al. PD-1 inhibitor combined with apatinib for advanced gastric or esophagogastric junction cancer: a retrospective study[J]. TRANSLATIONAL CANCER RESEARCH,2020,9.
APA Wei, Qing,Yuan, Xing,Li, Jingjing,Xu, Qi,&Ying, Jieer.(2020).PD-1 inhibitor combined with apatinib for advanced gastric or esophagogastric junction cancer: a retrospective study.TRANSLATIONAL CANCER RESEARCH,9.
MLA Wei, Qing,et al."PD-1 inhibitor combined with apatinib for advanced gastric or esophagogastric junction cancer: a retrospective study".TRANSLATIONAL CANCER RESEARCH 9(2020).

入库方式: OAI收割

来源:合肥物质科学研究院

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