Mismatch Repair Deficiency and Response to Immune Checkpoint Blockade

被引:199
|
作者
Lee, Valerie [1 ]
Murphy, Adrian [1 ]
Le, Dung T. [1 ]
Diaz, Luis A., Jr. [2 ,3 ]
机构
[1] Johns Hopkins Kimmel Canc Ctr, Baltimore, MD USA
[2] Johns Hopkins Kimmel Canc Ctr, Swim Across Amer Lab, Baltimore, MD USA
[3] Johns Hopkins Kimmel Canc Ctr, Ludwig Ctr Canc Genet & Therapeut, Baltimore, MD USA
来源
ONCOLOGIST | 2016年 / 21卷 / 10期
关键词
Microsatellite instability; DNA mismatch repair; Immunotherapy; Colonic neoplasms; Colorectal neoplasms; Hereditary nonpolyposis; LEVEL MICROSATELLITE INSTABILITY; COLORECTAL-CANCER PATIENTS; LYNCH-SYNDROME; GASTRIC-CANCER; ENDOMETRIAL CANCER; COLON-CANCER; BREAST-CANCER; ADJUVANT CHEMOTHERAPY; PROTEIN EXPRESSION; PROSTATE-CANCER;
D O I
10.1634/theoncologist.2016-0046
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
More than 1.6 million new cases of cancer will be diagnosed in the U.S. in 2016, resulting in more than 500,000 deaths. Although chemotherapy has been the mainstay of treatment in advanced cancers, immunotherapy development, particularly with PD-1 inhibitors, has changed the face of treatment for a number of tumor types. One example is the subset of tumors characterized by mismatch repair deficiency and microsatellite instability that are highly sensitive to PD-1 blockade. Hereditary forms of cancer have been noted for more than a century, but the molecular changes underlying mismatch repair-deficient tumors and subsequent microsatellite unstable tumors was not known until the early 1990s. In this review article, we discuss the history and pathophysiology of mismatch repair, the process of testing for mismatch repair deficiency and microsatellite instability, and the role of immunotherapy in this subset of cancers.
引用
收藏
页码:1200 / 1211
页数:12
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