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Fatal gastrointestinal toxicity with ipilimumab after BRAF/MEK inhibitor combination in a melanoma patient achieving pathological complete response
Approximately 50% of metastatic melanoma patients harbor BRAF mutations. Several treatment options including the combination of BRAF and MEK inhibitors (BRAF/MEKi) and immunotherapy (mainly anti CTLA-4 and anti PD-1 antibodies), have been shown to improve survival in these patients. Although preclin...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5302939/ https://www.ncbi.nlm.nih.gov/pubmed/27447748 http://dx.doi.org/10.18632/oncotarget.10651 |
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author | Gonzalez-Cao, Maria Boada, Aram Teixidó, Cristina Fernandez-Figueras, María Teresa Mayo, Clara Tresserra, Francesc Bustamante, Jean Viteri, Santiago Puertas, Enrique Santarpia, Mariacarmela Riso, Aldo Barron, Feliciano Karachaliou, Niki Rosell, Rafael |
author_facet | Gonzalez-Cao, Maria Boada, Aram Teixidó, Cristina Fernandez-Figueras, María Teresa Mayo, Clara Tresserra, Francesc Bustamante, Jean Viteri, Santiago Puertas, Enrique Santarpia, Mariacarmela Riso, Aldo Barron, Feliciano Karachaliou, Niki Rosell, Rafael |
author_sort | Gonzalez-Cao, Maria |
collection | PubMed |
description | Approximately 50% of metastatic melanoma patients harbor BRAF mutations. Several treatment options including the combination of BRAF and MEK inhibitors (BRAF/MEKi) and immunotherapy (mainly anti CTLA-4 and anti PD-1 antibodies), have been shown to improve survival in these patients. Although preclinical data support the synergistic effect of both modalities in combination, data confirming the activity and tolerability of these combinations are not yet available in the clinical setting. Herein, we report the case of a melanoma patient treated with sequential BRAF/MEKi (dabrafenib plus trametinib) followed by the anti CTLA-4 antibody ipilimumab who achieved a pathological complete response. Unfortunately, the patient died due to fatal gastrointestinal (GI) toxicity. Analysis of the BRAFV600E mutation in circulating tumoral DNA (ctDNA) from peripheral blood samples and serial tumor tissue biopsies throughout treatment demonstrated a good correlation with clinical evolution. |
format | Online Article Text |
id | pubmed-5302939 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53029392017-02-13 Fatal gastrointestinal toxicity with ipilimumab after BRAF/MEK inhibitor combination in a melanoma patient achieving pathological complete response Gonzalez-Cao, Maria Boada, Aram Teixidó, Cristina Fernandez-Figueras, María Teresa Mayo, Clara Tresserra, Francesc Bustamante, Jean Viteri, Santiago Puertas, Enrique Santarpia, Mariacarmela Riso, Aldo Barron, Feliciano Karachaliou, Niki Rosell, Rafael Oncotarget Research Paper Approximately 50% of metastatic melanoma patients harbor BRAF mutations. Several treatment options including the combination of BRAF and MEK inhibitors (BRAF/MEKi) and immunotherapy (mainly anti CTLA-4 and anti PD-1 antibodies), have been shown to improve survival in these patients. Although preclinical data support the synergistic effect of both modalities in combination, data confirming the activity and tolerability of these combinations are not yet available in the clinical setting. Herein, we report the case of a melanoma patient treated with sequential BRAF/MEKi (dabrafenib plus trametinib) followed by the anti CTLA-4 antibody ipilimumab who achieved a pathological complete response. Unfortunately, the patient died due to fatal gastrointestinal (GI) toxicity. Analysis of the BRAFV600E mutation in circulating tumoral DNA (ctDNA) from peripheral blood samples and serial tumor tissue biopsies throughout treatment demonstrated a good correlation with clinical evolution. Impact Journals LLC 2016-07-18 /pmc/articles/PMC5302939/ /pubmed/27447748 http://dx.doi.org/10.18632/oncotarget.10651 Text en Copyright: © 2016 Gonzalez-Cao et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Gonzalez-Cao, Maria Boada, Aram Teixidó, Cristina Fernandez-Figueras, María Teresa Mayo, Clara Tresserra, Francesc Bustamante, Jean Viteri, Santiago Puertas, Enrique Santarpia, Mariacarmela Riso, Aldo Barron, Feliciano Karachaliou, Niki Rosell, Rafael Fatal gastrointestinal toxicity with ipilimumab after BRAF/MEK inhibitor combination in a melanoma patient achieving pathological complete response |
title | Fatal gastrointestinal toxicity with ipilimumab after BRAF/MEK inhibitor combination in a melanoma patient achieving pathological complete response |
title_full | Fatal gastrointestinal toxicity with ipilimumab after BRAF/MEK inhibitor combination in a melanoma patient achieving pathological complete response |
title_fullStr | Fatal gastrointestinal toxicity with ipilimumab after BRAF/MEK inhibitor combination in a melanoma patient achieving pathological complete response |
title_full_unstemmed | Fatal gastrointestinal toxicity with ipilimumab after BRAF/MEK inhibitor combination in a melanoma patient achieving pathological complete response |
title_short | Fatal gastrointestinal toxicity with ipilimumab after BRAF/MEK inhibitor combination in a melanoma patient achieving pathological complete response |
title_sort | fatal gastrointestinal toxicity with ipilimumab after braf/mek inhibitor combination in a melanoma patient achieving pathological complete response |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5302939/ https://www.ncbi.nlm.nih.gov/pubmed/27447748 http://dx.doi.org/10.18632/oncotarget.10651 |
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