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Tumour mutation status and melanoma recurrence following a negative sentinel lymph node biopsy
BACKGROUND: A proportion of patients develop recurrence following a tumour-negative sentinel lymph node biopsy (SLNB). This study aimed to explore whether melanoma patients with BRAF or NRAS mutant tumours have an increased risk of developing disease recurrence following a negative SLNB compared to...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5959932/ https://www.ncbi.nlm.nih.gov/pubmed/29755118 http://dx.doi.org/10.1038/s41416-018-0088-8 |
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author | Adler, Nikki R. Wolfe, Rory McArthur, Grant A. Kelly, John W. Haydon, Andrew McLean, Catriona A. Mar, Victoria J. |
author_facet | Adler, Nikki R. Wolfe, Rory McArthur, Grant A. Kelly, John W. Haydon, Andrew McLean, Catriona A. Mar, Victoria J. |
author_sort | Adler, Nikki R. |
collection | PubMed |
description | BACKGROUND: A proportion of patients develop recurrence following a tumour-negative sentinel lymph node biopsy (SLNB). This study aimed to explore whether melanoma patients with BRAF or NRAS mutant tumours have an increased risk of developing disease recurrence following a negative SLNB compared to patients with wild-type tumours. METHODS: Prospective cohort study of melanoma patients at three tertiary referral centres in Melbourne, who underwent SLNB. Clinical, pathological and molecular characteristics and recurrence data were prospectively recorded. Multivariate Cox proportional hazards regression models estimated the adjusted hazard ratio (aHR) and corresponding 95% confidence interval (CI) for the association between mutation status and development of recurrence following a negative-SLNB. RESULTS: Overall, 344/477 (72.1%) patients had a negative SLNB. Of these, 54 (15.7%) developed subsequent recurrence. The risk of disease recurrence following a negative SLNB was increased for patients with either a BRAF or NRAS mutant tumour compared to wild-type tumours (aHR 1.92, 95% CI: 1.02–3.60, p = 0.04). CONCLUSION: Melanoma patients with BRAF or NRAS mutant tumours had an increased risk compared to patients with BRAF/NRAS wild-type tumours of developing disease recurrence following a tumour-negative SLNB. The findings also confirm the importance of continued surveillance to monitor for disease recurrence among SLNB-negative patients. |
format | Online Article Text |
id | pubmed-5959932 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59599322019-05-15 Tumour mutation status and melanoma recurrence following a negative sentinel lymph node biopsy Adler, Nikki R. Wolfe, Rory McArthur, Grant A. Kelly, John W. Haydon, Andrew McLean, Catriona A. Mar, Victoria J. Br J Cancer Article BACKGROUND: A proportion of patients develop recurrence following a tumour-negative sentinel lymph node biopsy (SLNB). This study aimed to explore whether melanoma patients with BRAF or NRAS mutant tumours have an increased risk of developing disease recurrence following a negative SLNB compared to patients with wild-type tumours. METHODS: Prospective cohort study of melanoma patients at three tertiary referral centres in Melbourne, who underwent SLNB. Clinical, pathological and molecular characteristics and recurrence data were prospectively recorded. Multivariate Cox proportional hazards regression models estimated the adjusted hazard ratio (aHR) and corresponding 95% confidence interval (CI) for the association between mutation status and development of recurrence following a negative-SLNB. RESULTS: Overall, 344/477 (72.1%) patients had a negative SLNB. Of these, 54 (15.7%) developed subsequent recurrence. The risk of disease recurrence following a negative SLNB was increased for patients with either a BRAF or NRAS mutant tumour compared to wild-type tumours (aHR 1.92, 95% CI: 1.02–3.60, p = 0.04). CONCLUSION: Melanoma patients with BRAF or NRAS mutant tumours had an increased risk compared to patients with BRAF/NRAS wild-type tumours of developing disease recurrence following a tumour-negative SLNB. The findings also confirm the importance of continued surveillance to monitor for disease recurrence among SLNB-negative patients. Nature Publishing Group UK 2018-05-14 2018-05-15 /pmc/articles/PMC5959932/ /pubmed/29755118 http://dx.doi.org/10.1038/s41416-018-0088-8 Text en © Cancer Research UK 2018 https://creativecommons.org/licenses/by/4.0/Note: This work is published under the standard license to publish agreement. After 12 months the work will become freely available and the license terms will switch to a Creative Commons Attribution 4.0 International licence (CC BY 4.0). |
spellingShingle | Article Adler, Nikki R. Wolfe, Rory McArthur, Grant A. Kelly, John W. Haydon, Andrew McLean, Catriona A. Mar, Victoria J. Tumour mutation status and melanoma recurrence following a negative sentinel lymph node biopsy |
title | Tumour mutation status and melanoma recurrence following a negative sentinel lymph node biopsy |
title_full | Tumour mutation status and melanoma recurrence following a negative sentinel lymph node biopsy |
title_fullStr | Tumour mutation status and melanoma recurrence following a negative sentinel lymph node biopsy |
title_full_unstemmed | Tumour mutation status and melanoma recurrence following a negative sentinel lymph node biopsy |
title_short | Tumour mutation status and melanoma recurrence following a negative sentinel lymph node biopsy |
title_sort | tumour mutation status and melanoma recurrence following a negative sentinel lymph node biopsy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5959932/ https://www.ncbi.nlm.nih.gov/pubmed/29755118 http://dx.doi.org/10.1038/s41416-018-0088-8 |
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