Immune checkpoint blockade therapy for BRAF mutant metastatic colorectal cancer: the efficacy, new strategies, and potential biomarkers

Abstract BRAF mutant metastatic colorectal cancer has long been considered a tumor with a poor prognosis and a poor response to chemotherapy. Despite the efficacy of targeted therapy with multi-targeted blockade of the mitogen-activated protein kinase (MAPK) signaling pathway has brought a glimmer o...

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Main Authors: Jie Zhong, Zijian Sun, Sheng Li, Liu Yang, Yuepeng Cao, Jun Bao
Format: Article
Language:English
Published: Springer 2023-06-01
Series:Discover Oncology
Subjects:
Online Access:https://doi.org/10.1007/s12672-023-00718-y
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author Jie Zhong
Zijian Sun
Sheng Li
Liu Yang
Yuepeng Cao
Jun Bao
author_facet Jie Zhong
Zijian Sun
Sheng Li
Liu Yang
Yuepeng Cao
Jun Bao
author_sort Jie Zhong
collection DOAJ
description Abstract BRAF mutant metastatic colorectal cancer has long been considered a tumor with a poor prognosis and a poor response to chemotherapy. Despite the efficacy of targeted therapy with multi-targeted blockade of the mitogen-activated protein kinase (MAPK) signaling pathway has brought a glimmer of hope to this group of patients, the need to improve treatment efficacy remains unmet, especially for the microsatellite stability/DNA proficient mismatch repair (MSS/pMMR) subtype. BRAF mutant colorectal cancer patients with high microsatellite instability/DNA deficient mismatch repair (MSI-H/dMMR) have high tumor mutation burden and abundant neoantigen, who are deemed as ones that could receive expected efficacy from immunotherapy. Generally, it is believed that MSS/pMMR colorectal cancer is an immunologically “cold” tumor that is insensitive to immunotherapy. However, targeted therapy combined with immune checkpoint blockade therapy seems to bring light to BRAF mutant colorectal cancer patients. In this review, we provide an overview of clinical efficacy and evolving new strategies concerning immune checkpoint blockade therapy for both MSI-H/dMMR and MSS/pMMR BRAF mutant metastatic colorectal cancer and discuss the potential biomarkers in the tumor immune microenvironment for predicting immunotherapeutic response in BRAF mutant colorectal cancer.
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spelling doaj.art-afff91d4332441949c021f600fc7d8dd2023-06-11T11:17:35ZengSpringerDiscover Oncology2730-60112023-06-0114111310.1007/s12672-023-00718-yImmune checkpoint blockade therapy for BRAF mutant metastatic colorectal cancer: the efficacy, new strategies, and potential biomarkersJie Zhong0Zijian Sun1Sheng Li2Liu Yang3Yuepeng Cao4Jun Bao5Department of Medical Oncology, The Affiliated Cancer Hospital of Nanjing Medical UniversityDepartment of Medical Oncology, The Affiliated Cancer Hospital of Nanjing Medical UniversityDepartment of Medical Oncology, The Affiliated Cancer Hospital of Nanjing Medical UniversityDepartment of Colorectal Surgery, The Affiliated Cancer Hospital of Nanjing Medical UniversityDepartment of Colorectal Surgery, The Affiliated Cancer Hospital of Nanjing Medical UniversityDepartment of Medical Oncology, The Affiliated Cancer Hospital of Nanjing Medical UniversityAbstract BRAF mutant metastatic colorectal cancer has long been considered a tumor with a poor prognosis and a poor response to chemotherapy. Despite the efficacy of targeted therapy with multi-targeted blockade of the mitogen-activated protein kinase (MAPK) signaling pathway has brought a glimmer of hope to this group of patients, the need to improve treatment efficacy remains unmet, especially for the microsatellite stability/DNA proficient mismatch repair (MSS/pMMR) subtype. BRAF mutant colorectal cancer patients with high microsatellite instability/DNA deficient mismatch repair (MSI-H/dMMR) have high tumor mutation burden and abundant neoantigen, who are deemed as ones that could receive expected efficacy from immunotherapy. Generally, it is believed that MSS/pMMR colorectal cancer is an immunologically “cold” tumor that is insensitive to immunotherapy. However, targeted therapy combined with immune checkpoint blockade therapy seems to bring light to BRAF mutant colorectal cancer patients. In this review, we provide an overview of clinical efficacy and evolving new strategies concerning immune checkpoint blockade therapy for both MSI-H/dMMR and MSS/pMMR BRAF mutant metastatic colorectal cancer and discuss the potential biomarkers in the tumor immune microenvironment for predicting immunotherapeutic response in BRAF mutant colorectal cancer.https://doi.org/10.1007/s12672-023-00718-yBRAF mutationColorectal cancerImmune checkpoint blockade therapyTargeted therapyPredictive biomarkers
spellingShingle Jie Zhong
Zijian Sun
Sheng Li
Liu Yang
Yuepeng Cao
Jun Bao
Immune checkpoint blockade therapy for BRAF mutant metastatic colorectal cancer: the efficacy, new strategies, and potential biomarkers
Discover Oncology
BRAF mutation
Colorectal cancer
Immune checkpoint blockade therapy
Targeted therapy
Predictive biomarkers
title Immune checkpoint blockade therapy for BRAF mutant metastatic colorectal cancer: the efficacy, new strategies, and potential biomarkers
title_full Immune checkpoint blockade therapy for BRAF mutant metastatic colorectal cancer: the efficacy, new strategies, and potential biomarkers
title_fullStr Immune checkpoint blockade therapy for BRAF mutant metastatic colorectal cancer: the efficacy, new strategies, and potential biomarkers
title_full_unstemmed Immune checkpoint blockade therapy for BRAF mutant metastatic colorectal cancer: the efficacy, new strategies, and potential biomarkers
title_short Immune checkpoint blockade therapy for BRAF mutant metastatic colorectal cancer: the efficacy, new strategies, and potential biomarkers
title_sort immune checkpoint blockade therapy for braf mutant metastatic colorectal cancer the efficacy new strategies and potential biomarkers
topic BRAF mutation
Colorectal cancer
Immune checkpoint blockade therapy
Targeted therapy
Predictive biomarkers
url https://doi.org/10.1007/s12672-023-00718-y
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