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Cardiac tamponade induced by dabrafenib and trametinib combination therapy for melanoma: Case report

RATIONALE: BRAF and MEK inhibitors (BRAF/MEKi) are targeted therapy for proto-oncogene BRAF mutated metastatic unresectable melanoma. Compared to monotherapy, an increased cardiovascular toxicity is reported with the combination of Dabrafenib and Trametinib. This case report documents Grade 4 cardia...

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Autores principales: Sundaram, Vinita Ruth, Abbas, Tahir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6221704/
https://www.ncbi.nlm.nih.gov/pubmed/30383630
http://dx.doi.org/10.1097/MD.0000000000012751
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author Sundaram, Vinita Ruth
Abbas, Tahir
author_facet Sundaram, Vinita Ruth
Abbas, Tahir
author_sort Sundaram, Vinita Ruth
collection PubMed
description RATIONALE: BRAF and MEK inhibitors (BRAF/MEKi) are targeted therapy for proto-oncogene BRAF mutated metastatic unresectable melanoma. Compared to monotherapy, an increased cardiovascular toxicity is reported with the combination of Dabrafenib and Trametinib. This case report documents Grade 4 cardiac treatment emergent adverse effect of pericardial effusion and cardiac tamponade induced by this combination therapy. PATIENT CONCERNS: A 52 year old man presented with clinical stage II unresectable melanoma with BRAF (V600E) mutation, was initiated on treatement with Dabrafenib and Trametinib. He complained of generalised edema and increased his weight by 27 kg. This progressed to shortness of breath and he underwent echocardiogram which revealed cardiac tamponade. DIAGNOSES: Emergent pericardiocentesis was performed. No definited pathology was demonstrated in laboratory analysis of pericardial fluid. Re- initiating treatment resulted in cardiac tamponade and pericardiotomy was performed by video-assisted thoracic surgical (VATS). Pericardial biopsy revealed nonspecific chronic inflammation. INTERVENTIONS: Discontinuation of treatment with Dabrafenib and Trametinib and diuretics resolved peripheral edema. Cardiac function normalized after pericardiocentesis and pericardiotomy. OUTCOMES: Treatment with Dabrafenib and Trametinib caused significant peripheral edema and pericardial effusion resulting in cardiac tamponade. Naranjo score suggests probable association of treatment induced pericardial effusion and cardiac tamponade. LESSONS: This is the first documented report of pericardial effusion and cardiac tamponade induced by Dabrafenib and Trametinib. Cardiac toxicity of BRAF/MEK inhibitors is rare but clinicans must monitor for treatment emergent adverse effects.
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spelling pubmed-62217042018-12-04 Cardiac tamponade induced by dabrafenib and trametinib combination therapy for melanoma: Case report Sundaram, Vinita Ruth Abbas, Tahir Medicine (Baltimore) Research Article RATIONALE: BRAF and MEK inhibitors (BRAF/MEKi) are targeted therapy for proto-oncogene BRAF mutated metastatic unresectable melanoma. Compared to monotherapy, an increased cardiovascular toxicity is reported with the combination of Dabrafenib and Trametinib. This case report documents Grade 4 cardiac treatment emergent adverse effect of pericardial effusion and cardiac tamponade induced by this combination therapy. PATIENT CONCERNS: A 52 year old man presented with clinical stage II unresectable melanoma with BRAF (V600E) mutation, was initiated on treatement with Dabrafenib and Trametinib. He complained of generalised edema and increased his weight by 27 kg. This progressed to shortness of breath and he underwent echocardiogram which revealed cardiac tamponade. DIAGNOSES: Emergent pericardiocentesis was performed. No definited pathology was demonstrated in laboratory analysis of pericardial fluid. Re- initiating treatment resulted in cardiac tamponade and pericardiotomy was performed by video-assisted thoracic surgical (VATS). Pericardial biopsy revealed nonspecific chronic inflammation. INTERVENTIONS: Discontinuation of treatment with Dabrafenib and Trametinib and diuretics resolved peripheral edema. Cardiac function normalized after pericardiocentesis and pericardiotomy. OUTCOMES: Treatment with Dabrafenib and Trametinib caused significant peripheral edema and pericardial effusion resulting in cardiac tamponade. Naranjo score suggests probable association of treatment induced pericardial effusion and cardiac tamponade. LESSONS: This is the first documented report of pericardial effusion and cardiac tamponade induced by Dabrafenib and Trametinib. Cardiac toxicity of BRAF/MEK inhibitors is rare but clinicans must monitor for treatment emergent adverse effects. Wolters Kluwer Health 2018-11-02 /pmc/articles/PMC6221704/ /pubmed/30383630 http://dx.doi.org/10.1097/MD.0000000000012751 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle Research Article
Sundaram, Vinita Ruth
Abbas, Tahir
Cardiac tamponade induced by dabrafenib and trametinib combination therapy for melanoma: Case report
title Cardiac tamponade induced by dabrafenib and trametinib combination therapy for melanoma: Case report
title_full Cardiac tamponade induced by dabrafenib and trametinib combination therapy for melanoma: Case report
title_fullStr Cardiac tamponade induced by dabrafenib and trametinib combination therapy for melanoma: Case report
title_full_unstemmed Cardiac tamponade induced by dabrafenib and trametinib combination therapy for melanoma: Case report
title_short Cardiac tamponade induced by dabrafenib and trametinib combination therapy for melanoma: Case report
title_sort cardiac tamponade induced by dabrafenib and trametinib combination therapy for melanoma: case report
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6221704/
https://www.ncbi.nlm.nih.gov/pubmed/30383630
http://dx.doi.org/10.1097/MD.0000000000012751
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