Immunotherapy in colorectal cancer: rationale, challenges and potential

被引:1306
作者
Ganesh, Karuna [1 ]
Stadler, Zsofia K. [1 ]
Cercek, Andrea [1 ]
Mendelsohn, Robin B. [1 ]
Shia, Jinru [2 ]
Segal, Neil H. [1 ]
Diaz, Luis A., Jr. [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Med, York Ave, New York, NY 10021 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Pathol, York Ave, New York, NY USA
关键词
MICROSATELLITE INSTABILITY DETECTION; TUMOR-ASSOCIATED MACROPHAGES; NIVOLUMAB PLUS IPILIMUMAB; MISMATCH REPAIR-DEFICIENT; DURABLE CLINICAL BENEFIT; PROMOTES T-CELL; PD-1; BLOCKADE; IMMUNE CELLS; COLON-CANCER; PHASE-I;
D O I
10.1038/s41575-019-0126-x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Following initial successes in melanoma treatment, immunotherapy has rapidly become established as a major treatment modality for multiple types of solid cancers, including a subset of colorectal cancers (CRCs). Two programmed cell death 1 (PD1)-blocking antibodies, pembrolizumab and nivolumab, have shown efficacy in patients with metastatic CRC that is mismatch-repair-deficient and microsatellite instability-high (dMMR-MSI-H), and have been granted accelerated FDA approval. In contrast to most other treatments for metastatic cancer, immunotherapy achieves long-term durable remission in a subset of patients, highlighting the tremendous promise of immunotherapy in treating dMMR-MSI-H metastatic CRC. Here, we review the clinical development of immune checkpoint inhibition in CRC leading to regulatory approvals for the treatment of dMMR-MSI-H CRC. We focus on new advances in expanding the efficacy of immunotherapy to early-stage CRC and CRC that is mismatch-repair-proficient and has low microsatellite instability (pMMR-MSI-L) and discuss emerging approaches for targeting the immune microenvironment, which might complement immune checkpoint inhibition.
引用
收藏
页码:361 / 375
页数:15
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