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Metastatic Colorectal Cancer Patient With Microsatellite Stability and BRAF(V600E) Mutation Showed a Complete Metabolic Response to PD-1 Blockade and Bevacizumab: A Case Report
A vast majority of colorectal cancer (CRC) patients with microsatellite stability (MSS) or proficient mismatch repair (pMMR) are refractory to immunotherapeutic strategies. The current research focusses on the combined treatment strategies for identification and optimization in order to improve the...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8112237/ https://www.ncbi.nlm.nih.gov/pubmed/33987088 http://dx.doi.org/10.3389/fonc.2021.652394 |
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author | Fang, Chongkai Lin, Jietao Zhang, Tao Luo, Jiajun Nie, Duorui Li, Meng Hu, Xue Zheng, Yating Huang, Xuewu Xiao, Zhiwei |
author_facet | Fang, Chongkai Lin, Jietao Zhang, Tao Luo, Jiajun Nie, Duorui Li, Meng Hu, Xue Zheng, Yating Huang, Xuewu Xiao, Zhiwei |
author_sort | Fang, Chongkai |
collection | PubMed |
description | A vast majority of colorectal cancer (CRC) patients with microsatellite stability (MSS) or proficient mismatch repair (pMMR) are refractory to immunotherapeutic strategies. The current research focusses on the combined treatment strategies for identification and optimization in order to improve the efficacy of immunotherapy among patients with microsatellite stability (MSS), who account for the majority of metastatic colorectal cancer (mCRC) cases. mCRC patients harboring MSS and the BRAF(V600E) mutation show a worse prognosis and barely benefit from immunotherapy. In this report, we discuss the case of a mCRC patient with MSS and BRAF(V600E) mutation, who exhibited significant response to the combined treatment with nivolumab and bevacizumab, and has been exhibiting a progression-free survival (PFS) of more than 17 months. Our findings indicate that combined anti-angiogenic therapy can improve the efficacy of immunotherapy, which results in the prolong survival of the patient. This is a case report on MSS and BRAF(V600E) colorectal cancer which presents with a response to immunotherapy and anti-angiogenic therapy. |
format | Online Article Text |
id | pubmed-8112237 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-81122372021-05-12 Metastatic Colorectal Cancer Patient With Microsatellite Stability and BRAF(V600E) Mutation Showed a Complete Metabolic Response to PD-1 Blockade and Bevacizumab: A Case Report Fang, Chongkai Lin, Jietao Zhang, Tao Luo, Jiajun Nie, Duorui Li, Meng Hu, Xue Zheng, Yating Huang, Xuewu Xiao, Zhiwei Front Oncol Oncology A vast majority of colorectal cancer (CRC) patients with microsatellite stability (MSS) or proficient mismatch repair (pMMR) are refractory to immunotherapeutic strategies. The current research focusses on the combined treatment strategies for identification and optimization in order to improve the efficacy of immunotherapy among patients with microsatellite stability (MSS), who account for the majority of metastatic colorectal cancer (mCRC) cases. mCRC patients harboring MSS and the BRAF(V600E) mutation show a worse prognosis and barely benefit from immunotherapy. In this report, we discuss the case of a mCRC patient with MSS and BRAF(V600E) mutation, who exhibited significant response to the combined treatment with nivolumab and bevacizumab, and has been exhibiting a progression-free survival (PFS) of more than 17 months. Our findings indicate that combined anti-angiogenic therapy can improve the efficacy of immunotherapy, which results in the prolong survival of the patient. This is a case report on MSS and BRAF(V600E) colorectal cancer which presents with a response to immunotherapy and anti-angiogenic therapy. Frontiers Media S.A. 2021-04-27 /pmc/articles/PMC8112237/ /pubmed/33987088 http://dx.doi.org/10.3389/fonc.2021.652394 Text en Copyright © 2021 Fang, Lin, Zhang, Luo, Nie, Li, Hu, Zheng, Huang and Xiao https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Fang, Chongkai Lin, Jietao Zhang, Tao Luo, Jiajun Nie, Duorui Li, Meng Hu, Xue Zheng, Yating Huang, Xuewu Xiao, Zhiwei Metastatic Colorectal Cancer Patient With Microsatellite Stability and BRAF(V600E) Mutation Showed a Complete Metabolic Response to PD-1 Blockade and Bevacizumab: A Case Report |
title | Metastatic Colorectal Cancer Patient With Microsatellite Stability and BRAF(V600E) Mutation Showed a Complete Metabolic Response to PD-1 Blockade and Bevacizumab: A Case Report |
title_full | Metastatic Colorectal Cancer Patient With Microsatellite Stability and BRAF(V600E) Mutation Showed a Complete Metabolic Response to PD-1 Blockade and Bevacizumab: A Case Report |
title_fullStr | Metastatic Colorectal Cancer Patient With Microsatellite Stability and BRAF(V600E) Mutation Showed a Complete Metabolic Response to PD-1 Blockade and Bevacizumab: A Case Report |
title_full_unstemmed | Metastatic Colorectal Cancer Patient With Microsatellite Stability and BRAF(V600E) Mutation Showed a Complete Metabolic Response to PD-1 Blockade and Bevacizumab: A Case Report |
title_short | Metastatic Colorectal Cancer Patient With Microsatellite Stability and BRAF(V600E) Mutation Showed a Complete Metabolic Response to PD-1 Blockade and Bevacizumab: A Case Report |
title_sort | metastatic colorectal cancer patient with microsatellite stability and braf(v600e) mutation showed a complete metabolic response to pd-1 blockade and bevacizumab: a case report |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8112237/ https://www.ncbi.nlm.nih.gov/pubmed/33987088 http://dx.doi.org/10.3389/fonc.2021.652394 |
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