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The melanoma-specific graded prognostic assessment does not adequately discriminate prognosis in a modern population with brain metastases from malignant melanoma

BACKGROUND: The melanoma-specific graded prognostic assessment (msGPA) assigns patients with brain metastases from malignant melanoma to 1 of 4 prognostic groups. It was largely derived using clinical data from patients treated in the era that preceded the development of newer therapies such as BRAF...

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Autores principales: Wilkins, Anna, Furness, Andrew, W Corbett, Richard, Bloomfield, Adam, Porta, Nuria, Morris, Stephen, Ali, Zohra, Larkin, James, Harrington, Kevin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4815790/
https://www.ncbi.nlm.nih.gov/pubmed/26484413
http://dx.doi.org/10.1038/bjc.2015.357
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author Wilkins, Anna
Furness, Andrew
W Corbett, Richard
Bloomfield, Adam
Porta, Nuria
Morris, Stephen
Ali, Zohra
Larkin, James
Harrington, Kevin
author_facet Wilkins, Anna
Furness, Andrew
W Corbett, Richard
Bloomfield, Adam
Porta, Nuria
Morris, Stephen
Ali, Zohra
Larkin, James
Harrington, Kevin
author_sort Wilkins, Anna
collection PubMed
description BACKGROUND: The melanoma-specific graded prognostic assessment (msGPA) assigns patients with brain metastases from malignant melanoma to 1 of 4 prognostic groups. It was largely derived using clinical data from patients treated in the era that preceded the development of newer therapies such as BRAF, MEK and immune checkpoint inhibitors. Therefore, its current relevance to patients diagnosed with brain metastases from malignant melanoma is unclear. This study is an external validation of the msGPA in two temporally distinct British populations. METHODS: Performance of the msGPA was assessed in Cohort I (1997–2008, n=231) and Cohort II (2008–2013, n=162) using Kaplan–Meier methods and Harrell's c-index of concordance. Cox regression was used to explore additional factors that may have prognostic relevance. RESULTS: The msGPA does not perform well as a prognostic score outside of the derivation cohort, with suboptimal statistical calibration and discrimination, particularly in those patients with an intermediate prognosis. Extra-cerebral metastases, leptomeningeal disease, age and potential use of novel targeted agents after brain metastases are diagnosed, should be incorporated into future prognostic models. CONCLUSIONS: An improved prognostic score is required to underpin high-quality randomised controlled trials in an area with a wide disparity in clinical care.
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spelling pubmed-48157902016-04-13 The melanoma-specific graded prognostic assessment does not adequately discriminate prognosis in a modern population with brain metastases from malignant melanoma Wilkins, Anna Furness, Andrew W Corbett, Richard Bloomfield, Adam Porta, Nuria Morris, Stephen Ali, Zohra Larkin, James Harrington, Kevin Br J Cancer Clinical Study BACKGROUND: The melanoma-specific graded prognostic assessment (msGPA) assigns patients with brain metastases from malignant melanoma to 1 of 4 prognostic groups. It was largely derived using clinical data from patients treated in the era that preceded the development of newer therapies such as BRAF, MEK and immune checkpoint inhibitors. Therefore, its current relevance to patients diagnosed with brain metastases from malignant melanoma is unclear. This study is an external validation of the msGPA in two temporally distinct British populations. METHODS: Performance of the msGPA was assessed in Cohort I (1997–2008, n=231) and Cohort II (2008–2013, n=162) using Kaplan–Meier methods and Harrell's c-index of concordance. Cox regression was used to explore additional factors that may have prognostic relevance. RESULTS: The msGPA does not perform well as a prognostic score outside of the derivation cohort, with suboptimal statistical calibration and discrimination, particularly in those patients with an intermediate prognosis. Extra-cerebral metastases, leptomeningeal disease, age and potential use of novel targeted agents after brain metastases are diagnosed, should be incorporated into future prognostic models. CONCLUSIONS: An improved prognostic score is required to underpin high-quality randomised controlled trials in an area with a wide disparity in clinical care. Nature Publishing Group 2015-11-03 2015-10-20 /pmc/articles/PMC4815790/ /pubmed/26484413 http://dx.doi.org/10.1038/bjc.2015.357 Text en Copyright © 2015 Cancer Research UK http://creativecommons.org/licenses/by/4.0/ This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Clinical Study
Wilkins, Anna
Furness, Andrew
W Corbett, Richard
Bloomfield, Adam
Porta, Nuria
Morris, Stephen
Ali, Zohra
Larkin, James
Harrington, Kevin
The melanoma-specific graded prognostic assessment does not adequately discriminate prognosis in a modern population with brain metastases from malignant melanoma
title The melanoma-specific graded prognostic assessment does not adequately discriminate prognosis in a modern population with brain metastases from malignant melanoma
title_full The melanoma-specific graded prognostic assessment does not adequately discriminate prognosis in a modern population with brain metastases from malignant melanoma
title_fullStr The melanoma-specific graded prognostic assessment does not adequately discriminate prognosis in a modern population with brain metastases from malignant melanoma
title_full_unstemmed The melanoma-specific graded prognostic assessment does not adequately discriminate prognosis in a modern population with brain metastases from malignant melanoma
title_short The melanoma-specific graded prognostic assessment does not adequately discriminate prognosis in a modern population with brain metastases from malignant melanoma
title_sort melanoma-specific graded prognostic assessment does not adequately discriminate prognosis in a modern population with brain metastases from malignant melanoma
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4815790/
https://www.ncbi.nlm.nih.gov/pubmed/26484413
http://dx.doi.org/10.1038/bjc.2015.357
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