MSI as a predictive factor for treatment outcome of gastroesophageal adenocarcinoma

被引:98
|
作者
van Velzen, M. J. M. [1 ]
Derks, S. [2 ]
van Grieken, N. C. T. [3 ]
Mohammad, N. Haj [4 ]
van Laarhoven, H. W. M. [1 ]
机构
[1] Univ Amsterdam, Amsterdam Univ Med Ctr, Canc Ctr Amsterdam, Dept Med Oncol, Amsterdam, Netherlands
[2] Vrije Univ Amsterdam, Amsterdam Univ Med Ctr, Canc Ctr Amsterdam, Dept Med Oncol, Amsterdam, Netherlands
[3] Vrije Univ Amsterdam, Amsterdam Univ Med Ctr, Canc Ctr Amsterdam, Dept Pathol, Amsterdam, Netherlands
[4] Univ Utrecht, Univ Med Ctr Utrecht, Dept Med Oncol, Utrecht, Netherlands
关键词
Gastroesophageal cancer; Microsatellite instability; Mismatch repair deficiency; Chemotherapy; Immunotherapy; Checkpoint inhibition; DNA MISMATCH REPAIR; MICROSATELLITE INSTABILITY; GASTRIC-CANCER; JUNCTION ADENOCARCINOMA; COLORECTAL-CANCER; ESOPHAGOGASTRIC CANCER; ADJUVANT CAPECITABINE; PD-1; BLOCKADE; OPEN-LABEL; STAGE-II;
D O I
10.1016/j.ctrv.2020.102024
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Gastroesophageal cancers are a major cause of death worldwide and treatment outcomes remain poor. Adequate predictive biomarkers have not been identified. Microsatellite instability (MSI) as a result of mismatch repair deficiency is present in four to twenty percent of gastroesophageal cancers and has been associated with favorable survival outcomes compared to microsatellite stable tumors. This prognostic advantage may be related to immunosurveillance, which may also explain the favorable response to immune checkpoint inhibition observed in MSI high (MSI-H) tumors. The value of conventional cytotoxic treatment in MSI-H tumors is unclear and results on its efficacy range from detrimental to beneficial effects. Here the recent data on MSI as a predictive factor for outcome of gastroesophageal cancer treatment is reviewed.
引用
收藏
页数:8
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