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Somatic and germline analyses of a long term melanoma survivor with a recurrent brain metastasis

BACKGROUND: Median overall survival (OS) of patients with melanoma brain metastases (MBM) is usually 6 months or less. There are rare reports of patients with treated MBM who survived for years. These outlier cases represent valuable opportunities to study the somatic and germline factors that may h...

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Autores principales: Weiss, Sarah, Darvishian, Farbod, Tadepalli, Jyothi, Shapiro, Richard, Golfinos, John, Pavlick, Anna, Polsky, David, Kirchhoff, Tomas, Osman, Iman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4657192/
https://www.ncbi.nlm.nih.gov/pubmed/26597176
http://dx.doi.org/10.1186/s12885-015-1927-0
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author Weiss, Sarah
Darvishian, Farbod
Tadepalli, Jyothi
Shapiro, Richard
Golfinos, John
Pavlick, Anna
Polsky, David
Kirchhoff, Tomas
Osman, Iman
author_facet Weiss, Sarah
Darvishian, Farbod
Tadepalli, Jyothi
Shapiro, Richard
Golfinos, John
Pavlick, Anna
Polsky, David
Kirchhoff, Tomas
Osman, Iman
author_sort Weiss, Sarah
collection PubMed
description BACKGROUND: Median overall survival (OS) of patients with melanoma brain metastases (MBM) is usually 6 months or less. There are rare reports of patients with treated MBM who survived for years. These outlier cases represent valuable opportunities to study the somatic and germline factors that may have influenced patient outcome and led to extended survival. CASE PRESENTATION: Here we report the clinical scenario of a 67 year old man with a recurrent brain metastasis from melanoma who has survived over 12 years post-resection. We review the literature relating to clinical and molecular variables associated with long term survival post-brain metastasis. We present the somatic characteristics of this individual patient’s tumor as well as an analysis of inherited genetic variants related to immune function. The patient’s resected brain tumor is BRAF V600E mutated, NRAS wild type (WT), and TERT C250T mutated. The patient is a carrier of germline variants in immunomodulatory loci associated with prolonged survival. CONCLUSIONS: Our data suggest that genetic variants in immunomodulatory loci may partially contribute to this patient’s unusually favorable outcome and should not be overlooked. With further and future investigation, knowledge of inherited single nucleotide polymorphisms (SNPs) may provide clinicians with more individualized prognostic information for melanoma patients, with potential implications for surveillance strategies and therapeutic interventions.
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spelling pubmed-46571922015-11-25 Somatic and germline analyses of a long term melanoma survivor with a recurrent brain metastasis Weiss, Sarah Darvishian, Farbod Tadepalli, Jyothi Shapiro, Richard Golfinos, John Pavlick, Anna Polsky, David Kirchhoff, Tomas Osman, Iman BMC Cancer Case Report BACKGROUND: Median overall survival (OS) of patients with melanoma brain metastases (MBM) is usually 6 months or less. There are rare reports of patients with treated MBM who survived for years. These outlier cases represent valuable opportunities to study the somatic and germline factors that may have influenced patient outcome and led to extended survival. CASE PRESENTATION: Here we report the clinical scenario of a 67 year old man with a recurrent brain metastasis from melanoma who has survived over 12 years post-resection. We review the literature relating to clinical and molecular variables associated with long term survival post-brain metastasis. We present the somatic characteristics of this individual patient’s tumor as well as an analysis of inherited genetic variants related to immune function. The patient’s resected brain tumor is BRAF V600E mutated, NRAS wild type (WT), and TERT C250T mutated. The patient is a carrier of germline variants in immunomodulatory loci associated with prolonged survival. CONCLUSIONS: Our data suggest that genetic variants in immunomodulatory loci may partially contribute to this patient’s unusually favorable outcome and should not be overlooked. With further and future investigation, knowledge of inherited single nucleotide polymorphisms (SNPs) may provide clinicians with more individualized prognostic information for melanoma patients, with potential implications for surveillance strategies and therapeutic interventions. BioMed Central 2015-11-23 /pmc/articles/PMC4657192/ /pubmed/26597176 http://dx.doi.org/10.1186/s12885-015-1927-0 Text en © Weiss et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Weiss, Sarah
Darvishian, Farbod
Tadepalli, Jyothi
Shapiro, Richard
Golfinos, John
Pavlick, Anna
Polsky, David
Kirchhoff, Tomas
Osman, Iman
Somatic and germline analyses of a long term melanoma survivor with a recurrent brain metastasis
title Somatic and germline analyses of a long term melanoma survivor with a recurrent brain metastasis
title_full Somatic and germline analyses of a long term melanoma survivor with a recurrent brain metastasis
title_fullStr Somatic and germline analyses of a long term melanoma survivor with a recurrent brain metastasis
title_full_unstemmed Somatic and germline analyses of a long term melanoma survivor with a recurrent brain metastasis
title_short Somatic and germline analyses of a long term melanoma survivor with a recurrent brain metastasis
title_sort somatic and germline analyses of a long term melanoma survivor with a recurrent brain metastasis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4657192/
https://www.ncbi.nlm.nih.gov/pubmed/26597176
http://dx.doi.org/10.1186/s12885-015-1927-0
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