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Bevacizumab as a steroid‐sparing agent during immunotherapy for melanoma brain metastases: A case series

BACKGROUND: Brain metastases are common in advanced melanoma and often necessitate corticosteroids such as dexamethasone to control symptoms and reduce peritumoral edema. Immunotherapy improves survival in metastatic melanoma, but concomitant treatment with corticosteroids may reduce efficacy. Here,...

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Autores principales: Banks, Patricia D., Lasocki, Arian, Lau, Peter K. H., Sandhu, Shahneen, McArthur, Grant, Shackleton, Mark
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/PMC6427059/
https://www.ncbi.nlm.nih.gov/pubmed/30937392
http://dx.doi.org/10.1002/hsr2.115
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author Banks, Patricia D.
Lasocki, Arian
Lau, Peter K. H.
Sandhu, Shahneen
McArthur, Grant
Shackleton, Mark
author_facet Banks, Patricia D.
Lasocki, Arian
Lau, Peter K. H.
Sandhu, Shahneen
McArthur, Grant
Shackleton, Mark
author_sort Banks, Patricia D.
collection PubMed
description BACKGROUND: Brain metastases are common in advanced melanoma and often necessitate corticosteroids such as dexamethasone to control symptoms and reduce peritumoral edema. Immunotherapy improves survival in metastatic melanoma, but concomitant treatment with corticosteroids may reduce efficacy. Here, we report the use of bevacizumab, a vascular endothelial growth factor (VEGF) inhibitor, as a steroid‐sparing agent in melanoma patients with brain metastases treated with immunotherapy. METHODS: Medical records and imaging were retrospectively analyzed for melanoma patients with brain metastases who received bevacizumab at our institution between 2012 and 2017. RESULTS: 12 melanoma patients with brain metastases received bevacizumab (5‐7.5 mg/kg Q2‐3 W; median 4 cycles, range 1‐9). Patients were BRAF wild‐type or resistant to BRAF/MEK inhibitor therapy. All had progressive intracranial disease after prior resection, stereotactic radiosurgery and/or whole brain radiotherapy, and up to four lines of previous systemic treatment. Prior to bevacizumab, all patients had radiologically defined peritumoral edema and nine required dexamethasone for symptom control. In 10 evaluable patients, six reduced their dexamethasone dose by more than 50%, and eight displayed reduced edema 4 weeks after bevacizumab. Seven patients experienced adverse events possibly related to bevacizumab, including intracranial hemorrhage, hypertension, and gastrointestinal bleeding. Ten patients received immunotherapy after bevacizumab. Five patients survived more than 6 months, including one who remained disease‐free after 4 years and without neurological deficit despite being hemiplegic from edematous brain metastases prior to bevacizumab. CONCLUSION: In 12 very poor prognosis melanoma patients with brain metastases, bevacizumab was well‐tolerated, associated with improved symptoms and reduced peritumoral edema despite weaning steroids, and facilitated treatment with immunotherapy that provided durable survival in a substantial proportion of cases.
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spelling pubmed-64270592019-04-01 Bevacizumab as a steroid‐sparing agent during immunotherapy for melanoma brain metastases: A case series Banks, Patricia D. Lasocki, Arian Lau, Peter K. H. Sandhu, Shahneen McArthur, Grant Shackleton, Mark Health Sci Rep Research Articles BACKGROUND: Brain metastases are common in advanced melanoma and often necessitate corticosteroids such as dexamethasone to control symptoms and reduce peritumoral edema. Immunotherapy improves survival in metastatic melanoma, but concomitant treatment with corticosteroids may reduce efficacy. Here, we report the use of bevacizumab, a vascular endothelial growth factor (VEGF) inhibitor, as a steroid‐sparing agent in melanoma patients with brain metastases treated with immunotherapy. METHODS: Medical records and imaging were retrospectively analyzed for melanoma patients with brain metastases who received bevacizumab at our institution between 2012 and 2017. RESULTS: 12 melanoma patients with brain metastases received bevacizumab (5‐7.5 mg/kg Q2‐3 W; median 4 cycles, range 1‐9). Patients were BRAF wild‐type or resistant to BRAF/MEK inhibitor therapy. All had progressive intracranial disease after prior resection, stereotactic radiosurgery and/or whole brain radiotherapy, and up to four lines of previous systemic treatment. Prior to bevacizumab, all patients had radiologically defined peritumoral edema and nine required dexamethasone for symptom control. In 10 evaluable patients, six reduced their dexamethasone dose by more than 50%, and eight displayed reduced edema 4 weeks after bevacizumab. Seven patients experienced adverse events possibly related to bevacizumab, including intracranial hemorrhage, hypertension, and gastrointestinal bleeding. Ten patients received immunotherapy after bevacizumab. Five patients survived more than 6 months, including one who remained disease‐free after 4 years and without neurological deficit despite being hemiplegic from edematous brain metastases prior to bevacizumab. CONCLUSION: In 12 very poor prognosis melanoma patients with brain metastases, bevacizumab was well‐tolerated, associated with improved symptoms and reduced peritumoral edema despite weaning steroids, and facilitated treatment with immunotherapy that provided durable survival in a substantial proportion of cases. John Wiley and Sons Inc. 2019-02-01 /pmc/articles/PMC6427059/ /pubmed/30937392 http://dx.doi.org/10.1002/hsr2.115 Text en © 2019 The Authors. Health Science Reports published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Banks, Patricia D.
Lasocki, Arian
Lau, Peter K. H.
Sandhu, Shahneen
McArthur, Grant
Shackleton, Mark
Bevacizumab as a steroid‐sparing agent during immunotherapy for melanoma brain metastases: A case series
title Bevacizumab as a steroid‐sparing agent during immunotherapy for melanoma brain metastases: A case series
title_full Bevacizumab as a steroid‐sparing agent during immunotherapy for melanoma brain metastases: A case series
title_fullStr Bevacizumab as a steroid‐sparing agent during immunotherapy for melanoma brain metastases: A case series
title_full_unstemmed Bevacizumab as a steroid‐sparing agent during immunotherapy for melanoma brain metastases: A case series
title_short Bevacizumab as a steroid‐sparing agent during immunotherapy for melanoma brain metastases: A case series
title_sort bevacizumab as a steroid‐sparing agent during immunotherapy for melanoma brain metastases: a case series
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6427059/
https://www.ncbi.nlm.nih.gov/pubmed/30937392
http://dx.doi.org/10.1002/hsr2.115
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