Cargando…
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...
Autores principales: | , , , , , , , , , |
---|---|
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 |
_version_ | 1783494660827643904 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7004095 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT holbrookkourtney intracranialantitumoractivitywithencorafenibplusbinimetinibinpatientswithmelanomabrainmetastasesacaseseries AT lutzkyjose intracranialantitumoractivitywithencorafenibplusbinimetinibinpatientswithmelanomabrainmetastasesacaseseries AT daviesmichaela intracranialantitumoractivitywithencorafenibplusbinimetinibinpatientswithmelanomabrainmetastasesacaseseries AT davisjessicamichaud intracranialantitumoractivitywithencorafenibplusbinimetinibinpatientswithmelanomabrainmetastasesacaseseries AT glitzaisabellac intracranialantitumoractivitywithencorafenibplusbinimetinibinpatientswithmelanomabrainmetastasesacaseseries AT amariarodaben intracranialantitumoractivitywithencorafenibplusbinimetinibinpatientswithmelanomabrainmetastasesacaseseries AT diabadi intracranialantitumoractivitywithencorafenibplusbinimetinibinpatientswithmelanomabrainmetastasesacaseseries AT patelsapnap intracranialantitumoractivitywithencorafenibplusbinimetinibinpatientswithmelanomabrainmetastasesacaseseries AT aminasim intracranialantitumoractivitywithencorafenibplusbinimetinibinpatientswithmelanomabrainmetastasesacaseseries AT tawbihussein intracranialantitumoractivitywithencorafenibplusbinimetinibinpatientswithmelanomabrainmetastasesacaseseries |