Research Progress of Immune Checkpoint Inhibitor Therapy for BRAF Mutation 
in Non-small Cell Lung Cancer

BRAF gene mutation is found in about 2%-4% of the patients with non-small cell lung cancer (NSCLC). This type of NSCLC is characterized by high malignancy, low efficacy of chemotherapy and poor prognosis. Although the combination treatment of BRAF inhibitor and MEK inhibitor has achieved remarkable...

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Main Authors: Xia LIU, Diansheng ZHONG
Format: Article
Language:zho
Published: Chinese Anti-Cancer Association; Chinese Antituberculosis Association 2019-09-01
Series:Chinese Journal of Lung Cancer
Subjects:
Online Access:http://dx.doi.org/10.3779/j.issn.1009-3419.2019.09.06
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spelling doaj-7633feaecefa401f85d00436ec1ac1ec2020-11-25T01:29:11ZzhoChinese Anti-Cancer Association; Chinese Antituberculosis AssociationChinese Journal of Lung Cancer1009-34191999-61872019-09-0122958358910.3779/j.issn.1009-3419.2019.09.06Research Progress of Immune Checkpoint Inhibitor Therapy for BRAF Mutation 
in Non-small Cell Lung CancerXia LIU0Diansheng ZHONG1Department of Medical Oncology, Tianjin Medical University General Hospital, Tianjin 300052, ChinaDepartment of Medical Oncology, Tianjin Medical University General Hospital, Tianjin 300052, ChinaBRAF gene mutation is found in about 2%-4% of the patients with non-small cell lung cancer (NSCLC). This type of NSCLC is characterized by high malignancy, low efficacy of chemotherapy and poor prognosis. Although the combination treatment of BRAF inhibitor and MEK inhibitor has achieved remarkable results in advanced NSCLC patients with BRAF V600E mutation, which has been written into the National Comprehensive Cancer Network (NCCN) guidelines, severe side effects of the combination therapy are frequently observed. There isn’t effective treatment strategy after drug resistance, and targeted therapy for non-V600E mutation patients is still lacking. In this paper, we summarized the researches on expression of immune markers in NSCLC patients with mutant BRAF and analyzed the studies on efficacy of immune checkpoint inhibitor (ICI), so as to provide more options for prolonging survival of the patients.http://dx.doi.org/10.3779/j.issn.1009-3419.2019.09.06Lung neoplasmsV-raf murine sar-coma viral oncogene homolog B1Immune checkpoint inhibitor therapy
collection DOAJ
language zho
format Article
sources DOAJ
author Xia LIU
Diansheng ZHONG
spellingShingle Xia LIU
Diansheng ZHONG
Research Progress of Immune Checkpoint Inhibitor Therapy for BRAF Mutation 
in Non-small Cell Lung Cancer
Chinese Journal of Lung Cancer
Lung neoplasms
V-raf murine sar-coma viral oncogene homolog B1
Immune checkpoint inhibitor therapy
author_facet Xia LIU
Diansheng ZHONG
author_sort Xia LIU
title Research Progress of Immune Checkpoint Inhibitor Therapy for BRAF Mutation 
in Non-small Cell Lung Cancer
title_short Research Progress of Immune Checkpoint Inhibitor Therapy for BRAF Mutation 
in Non-small Cell Lung Cancer
title_full Research Progress of Immune Checkpoint Inhibitor Therapy for BRAF Mutation 
in Non-small Cell Lung Cancer
title_fullStr Research Progress of Immune Checkpoint Inhibitor Therapy for BRAF Mutation 
in Non-small Cell Lung Cancer
title_full_unstemmed Research Progress of Immune Checkpoint Inhibitor Therapy for BRAF Mutation 
in Non-small Cell Lung Cancer
title_sort research progress of immune checkpoint inhibitor therapy for braf mutation 
in non-small cell lung cancer
publisher Chinese Anti-Cancer Association; Chinese Antituberculosis Association
series Chinese Journal of Lung Cancer
issn 1009-3419
1999-6187
publishDate 2019-09-01
description BRAF gene mutation is found in about 2%-4% of the patients with non-small cell lung cancer (NSCLC). This type of NSCLC is characterized by high malignancy, low efficacy of chemotherapy and poor prognosis. Although the combination treatment of BRAF inhibitor and MEK inhibitor has achieved remarkable results in advanced NSCLC patients with BRAF V600E mutation, which has been written into the National Comprehensive Cancer Network (NCCN) guidelines, severe side effects of the combination therapy are frequently observed. There isn’t effective treatment strategy after drug resistance, and targeted therapy for non-V600E mutation patients is still lacking. In this paper, we summarized the researches on expression of immune markers in NSCLC patients with mutant BRAF and analyzed the studies on efficacy of immune checkpoint inhibitor (ICI), so as to provide more options for prolonging survival of the patients.
topic Lung neoplasms
V-raf murine sar-coma viral oncogene homolog B1
Immune checkpoint inhibitor therapy
url http://dx.doi.org/10.3779/j.issn.1009-3419.2019.09.06
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AT dianshengzhong researchprogressofimmunecheckpointinhibitortherapyforbrafmutationinnonsmallcelllungcancer
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