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Phase I trial of pembrolizumab plus vemurafenib and cobimetinib in patients with metastatic melanoma
BACKGROUND: Preclinical and translational evidence suggest BRAF/MEK inhibitors modulate the tumor microenvironment (TME), providing rationale for combination with immunotherapy. METHODS: This investigator-initiated, phase I trial evaluated pembrolizumab, vemurafenib, and cobimetinib in patients with...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9727229/ https://www.ncbi.nlm.nih.gov/pubmed/36505793 http://dx.doi.org/10.3389/fonc.2022.1022496 |
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author | Shaikh, Saba S. Zang, Yan Hanmer, Janel Wang, Hong Lin, Yan Davar, Diwakar Zarour, Hassane M. Kirkwood, John M. Najjar, Yana G. |
author_facet | Shaikh, Saba S. Zang, Yan Hanmer, Janel Wang, Hong Lin, Yan Davar, Diwakar Zarour, Hassane M. Kirkwood, John M. Najjar, Yana G. |
author_sort | Shaikh, Saba S. |
collection | PubMed |
description | BACKGROUND: Preclinical and translational evidence suggest BRAF/MEK inhibitors modulate the tumor microenvironment (TME), providing rationale for combination with immunotherapy. METHODS: This investigator-initiated, phase I trial evaluated pembrolizumab, vemurafenib, and cobimetinib in patients with untreated, BRAFV600E/K mutant advanced melanoma. The first 4 patients received vemurafenib with pembrolizumab, and the next 5 patients received vemurafenib and cobimetinib with pembrolizumab. Primary endpoints: safety and maximum tolerated dose of the triplet. SECONDARY ENDPOINTS: objective response rate (ORR), progression-free survival (PFS), overall survival (OS), and quality of life (QoL). The trial was closed after enrollment of 9 (planned 30) patients due to dose-limiting toxicity (DLT). Study NCT02818023 was approved by the IRB, and all patients provided informed consent. RESULTS: Patients received a median of 6 cycles of therapy. 8 of 9 experienced drug-related grade 3/4 AEs. DLTs included dermatitis (n=8), hepatitis (n=1), QTc prolongation (n=1), and arthralgias (n=1 each). QoL assessments identified a clinically significant decrease in self assessed QoL at 1 year compared to baseline (0.38 v 0.43). Median PFS was 20.7 months and median OS was 23.8 months for vemurafenib with pembrolizumab. Median PFS and OS were not reached for patients receiving triple therapy. ORR in the overall cohort was 78% (7/9). 2 patients experienced a complete response, 5 had a partial response, 1 had stable disease, and 1 had progressive disease. 4 patients had ongoing responses at data analysis. Peripheral blood flow cytometry identified significantly decreased PD1 expression on CD4+ T-cells at 3 and 9 weeks compared to baseline, not corresponding to clinical response. CONCLUSIONS: Triple therapy with vemurafenib, cobimetinib and pembrolizumab is associated with high response rates but significant adverse events, leading to early study closure. |
format | Online Article Text |
id | pubmed-9727229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97272292022-12-08 Phase I trial of pembrolizumab plus vemurafenib and cobimetinib in patients with metastatic melanoma Shaikh, Saba S. Zang, Yan Hanmer, Janel Wang, Hong Lin, Yan Davar, Diwakar Zarour, Hassane M. Kirkwood, John M. Najjar, Yana G. Front Oncol Oncology BACKGROUND: Preclinical and translational evidence suggest BRAF/MEK inhibitors modulate the tumor microenvironment (TME), providing rationale for combination with immunotherapy. METHODS: This investigator-initiated, phase I trial evaluated pembrolizumab, vemurafenib, and cobimetinib in patients with untreated, BRAFV600E/K mutant advanced melanoma. The first 4 patients received vemurafenib with pembrolizumab, and the next 5 patients received vemurafenib and cobimetinib with pembrolizumab. Primary endpoints: safety and maximum tolerated dose of the triplet. SECONDARY ENDPOINTS: objective response rate (ORR), progression-free survival (PFS), overall survival (OS), and quality of life (QoL). The trial was closed after enrollment of 9 (planned 30) patients due to dose-limiting toxicity (DLT). Study NCT02818023 was approved by the IRB, and all patients provided informed consent. RESULTS: Patients received a median of 6 cycles of therapy. 8 of 9 experienced drug-related grade 3/4 AEs. DLTs included dermatitis (n=8), hepatitis (n=1), QTc prolongation (n=1), and arthralgias (n=1 each). QoL assessments identified a clinically significant decrease in self assessed QoL at 1 year compared to baseline (0.38 v 0.43). Median PFS was 20.7 months and median OS was 23.8 months for vemurafenib with pembrolizumab. Median PFS and OS were not reached for patients receiving triple therapy. ORR in the overall cohort was 78% (7/9). 2 patients experienced a complete response, 5 had a partial response, 1 had stable disease, and 1 had progressive disease. 4 patients had ongoing responses at data analysis. Peripheral blood flow cytometry identified significantly decreased PD1 expression on CD4+ T-cells at 3 and 9 weeks compared to baseline, not corresponding to clinical response. CONCLUSIONS: Triple therapy with vemurafenib, cobimetinib and pembrolizumab is associated with high response rates but significant adverse events, leading to early study closure. Frontiers Media S.A. 2022-11-23 /pmc/articles/PMC9727229/ /pubmed/36505793 http://dx.doi.org/10.3389/fonc.2022.1022496 Text en Copyright © 2022 Shaikh, Zang, Hanmer, Wang, Lin, Davar, Zarour, Kirkwood and Najjar 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 Shaikh, Saba S. Zang, Yan Hanmer, Janel Wang, Hong Lin, Yan Davar, Diwakar Zarour, Hassane M. Kirkwood, John M. Najjar, Yana G. Phase I trial of pembrolizumab plus vemurafenib and cobimetinib in patients with metastatic melanoma |
title | Phase I trial of pembrolizumab plus vemurafenib and cobimetinib in patients with metastatic melanoma |
title_full | Phase I trial of pembrolizumab plus vemurafenib and cobimetinib in patients with metastatic melanoma |
title_fullStr | Phase I trial of pembrolizumab plus vemurafenib and cobimetinib in patients with metastatic melanoma |
title_full_unstemmed | Phase I trial of pembrolizumab plus vemurafenib and cobimetinib in patients with metastatic melanoma |
title_short | Phase I trial of pembrolizumab plus vemurafenib and cobimetinib in patients with metastatic melanoma |
title_sort | phase i trial of pembrolizumab plus vemurafenib and cobimetinib in patients with metastatic melanoma |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9727229/ https://www.ncbi.nlm.nih.gov/pubmed/36505793 http://dx.doi.org/10.3389/fonc.2022.1022496 |
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