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Intracranial antitumor activity with encorafenib plus binimetinib in patients with melanoma brain metastases: A case series

BACKGROUND: Sixty percent of patients with stage IV melanoma may develop brain metastases, which result in significantly increased morbidity and a poor overall prognosis. Phase 3 studies of melanoma usually exclude patients with untreated brain metastases; therefore, clinical data for intracranial r...

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Autores principales: Holbrook, Kourtney, Lutzky, Jose, Davies, Michael A., Davis, Jessica Michaud, Glitza, Isabella C., Amaria, Rodabe N., Diab, Adi, Patel, Sapna P., Amin, Asim, Tawbi, Hussein
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7004095/
https://www.ncbi.nlm.nih.gov/pubmed/31658370
http://dx.doi.org/10.1002/cncr.32547
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author Holbrook, Kourtney
Lutzky, Jose
Davies, Michael A.
Davis, Jessica Michaud
Glitza, Isabella C.
Amaria, Rodabe N.
Diab, Adi
Patel, Sapna P.
Amin, Asim
Tawbi, Hussein
author_facet Holbrook, Kourtney
Lutzky, Jose
Davies, Michael A.
Davis, Jessica Michaud
Glitza, Isabella C.
Amaria, Rodabe N.
Diab, Adi
Patel, Sapna P.
Amin, Asim
Tawbi, Hussein
author_sort Holbrook, Kourtney
collection PubMed
description BACKGROUND: Sixty percent of patients with stage IV melanoma may develop brain metastases, which result in significantly increased morbidity and a poor overall prognosis. Phase 3 studies of melanoma usually exclude patients with untreated brain metastases; therefore, clinical data for intracranial responses to treatments are limited. METHODS: A multicenter, retrospective case series investigation of consecutive BRAF‐mutant patients with melanoma brain metastases (MBMs) treated with a combination of BRAF inhibitor encorafenib and MEK inhibitor binimetinib was conducted to evaluate the antitumor response. Assessments included the intracranial, extracranial, and global objective response rates (according to the modified Response Evaluation Criteria in Solid Tumors, version 1.1); the clinical benefit rate; the time to response; the duration of response; and safety. RESULTS: A total of 24 patients with stage IV BRAF‐mutant MBMs treated with encorafenib plus binimetinib in 3 centers in the United States were included. Patients had received a median of 2.5 prior lines of treatment, and 88% had prior treatment with BRAF/MEK inhibitors. The intracranial objective response rate was 33%, and the clinical benefit rate was 63%. The median time to a response was 6 weeks, and the median duration of response was 22 weeks. Among the 21 patients with MBMs and prior BRAF/MEK inhibitor treatment, the intracranial objective response rate was 24%, and the clinical benefit rate was 57%. Similar outcomes were observed for extracranial and global responses. The safety profile for encorafenib plus binimetinib was similar to that observed in patients with melanoma without brain metastases. CONCLUSIONS: Combination therapy with encorafenib plus binimetinib elicited intracranial activity in patients with BRAF‐mutant MBMs, including patients previously treated with BRAF/MEK inhibitors. Further prospective studies are warranted and ongoing.
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spelling pubmed-70040952020-02-11 Intracranial antitumor activity with encorafenib plus binimetinib in patients with melanoma brain metastases: A case series Holbrook, Kourtney Lutzky, Jose Davies, Michael A. Davis, Jessica Michaud Glitza, Isabella C. Amaria, Rodabe N. Diab, Adi Patel, Sapna P. Amin, Asim Tawbi, Hussein Cancer Original Articles BACKGROUND: Sixty percent of patients with stage IV melanoma may develop brain metastases, which result in significantly increased morbidity and a poor overall prognosis. Phase 3 studies of melanoma usually exclude patients with untreated brain metastases; therefore, clinical data for intracranial responses to treatments are limited. METHODS: A multicenter, retrospective case series investigation of consecutive BRAF‐mutant patients with melanoma brain metastases (MBMs) treated with a combination of BRAF inhibitor encorafenib and MEK inhibitor binimetinib was conducted to evaluate the antitumor response. Assessments included the intracranial, extracranial, and global objective response rates (according to the modified Response Evaluation Criteria in Solid Tumors, version 1.1); the clinical benefit rate; the time to response; the duration of response; and safety. RESULTS: A total of 24 patients with stage IV BRAF‐mutant MBMs treated with encorafenib plus binimetinib in 3 centers in the United States were included. Patients had received a median of 2.5 prior lines of treatment, and 88% had prior treatment with BRAF/MEK inhibitors. The intracranial objective response rate was 33%, and the clinical benefit rate was 63%. The median time to a response was 6 weeks, and the median duration of response was 22 weeks. Among the 21 patients with MBMs and prior BRAF/MEK inhibitor treatment, the intracranial objective response rate was 24%, and the clinical benefit rate was 57%. Similar outcomes were observed for extracranial and global responses. The safety profile for encorafenib plus binimetinib was similar to that observed in patients with melanoma without brain metastases. CONCLUSIONS: Combination therapy with encorafenib plus binimetinib elicited intracranial activity in patients with BRAF‐mutant MBMs, including patients previously treated with BRAF/MEK inhibitors. Further prospective studies are warranted and ongoing. John Wiley and Sons Inc. 2019-10-28 2020-02-01 /pmc/articles/PMC7004095/ /pubmed/31658370 http://dx.doi.org/10.1002/cncr.32547 Text en © 2019 The Authors. Cancer published by Wiley Periodicals, Inc. on behalf of American Cancer Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Holbrook, Kourtney
Lutzky, Jose
Davies, Michael A.
Davis, Jessica Michaud
Glitza, Isabella C.
Amaria, Rodabe N.
Diab, Adi
Patel, Sapna P.
Amin, Asim
Tawbi, Hussein
Intracranial antitumor activity with encorafenib plus binimetinib in patients with melanoma brain metastases: A case series
title Intracranial antitumor activity with encorafenib plus binimetinib in patients with melanoma brain metastases: A case series
title_full Intracranial antitumor activity with encorafenib plus binimetinib in patients with melanoma brain metastases: A case series
title_fullStr Intracranial antitumor activity with encorafenib plus binimetinib in patients with melanoma brain metastases: A case series
title_full_unstemmed Intracranial antitumor activity with encorafenib plus binimetinib in patients with melanoma brain metastases: A case series
title_short Intracranial antitumor activity with encorafenib plus binimetinib in patients with melanoma brain metastases: A case series
title_sort intracranial antitumor activity with encorafenib plus binimetinib in patients with melanoma brain metastases: a case series
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7004095/
https://www.ncbi.nlm.nih.gov/pubmed/31658370
http://dx.doi.org/10.1002/cncr.32547
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