Tumour mutation status and melanoma recurrence following a negative sentinel lymph node biopsy
Web of Science
AuthorAdler, NR; Wolfe, R; McArthur, GA; Kelly, JW; Haydon, A; McLean, CA; Mar, VJ
Source TitleBritish Journal of Cancer
PublisherNATURE PUBLISHING GROUP
AffiliationMelbourne Medical School
Florey Department of Neuroscience and Mental Health
Document TypeJournal Article
CitationsAdler, N. R., Wolfe, R., McArthur, G. A., Kelly, J. W., Haydon, A., McLean, C. A. & Mar, V. J. (2018). Tumour mutation status and melanoma recurrence following a negative sentinel lymph node biopsy. BRITISH JOURNAL OF CANCER, 118 (10), pp.1289-1295. https://doi.org/10.1038/s41416-018-0088-8.
Access StatusOpen Access
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.
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