Evidence map›Paper›PMID 42303829›Full record

ArticleBritish journal of cancer2026

Implications of wait times for sentinel node biopsy on melanoma disease progression, micrometastatic tumour burden and survival outcomes in the modern treatment era.

Sofia O Breeze, Martin J Heaton, Andrew P Snelling, Jennifer J Garioch, Jenny P Nobes, Marc D Moncrieff

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Article in British journal of cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Sofia O BreezeNorwich Medical School, University of East Anglia, Norwich, UK.ORCID http://orcid.org/0009-0005-7780-8942
Martin J HeatonDepartment of Plastic & Reconstructive Surgery, Norfolk and Norwich University Hospitals NHS Foundation Trust, Norwich, UK.
Andrew P SnellingDepartment of Plastic & Reconstructive Surgery, Norfolk and Norwich University Hospitals NHS Foundation Trust, Norwich, UK.
Jennifer J GariochNorwich Medical School, University of East Anglia, Norwich, UK.
Jenny P NobesNorwich Medical School, University of East Anglia, Norwich, UK.
Marc D MoncrieffNorwich Medical School, University of East Anglia, Norwich, UK. marc.moncrieff@nnuh.nhs.uk.ORCID http://orcid.org/0000-0003-4492-235X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSentinel node biopsy (SNB) predicts long-term melanoma outcomes and advises referrals for adjuvant systemic therapy (AST). Concerns regarding the impact of treatment delays on clinical outcomes remain.

methodsA UK retrospective cohort study at a supra-regional centre was performed, including 1625 patients listed for SNB between 2010-23. Three parameters were investigated: disease progression, micrometastatic burden, and disease-specific survival. Time-to-SNB was stratified as early (≤90days) or late (>90days), with a subgroup analysis accounting for AST use (2017-23). Sensitivity analyses calculated a wait-time threshold beyond which worsens survival outcomes.

resultsMedian time-to-SNB was 68 days (IQR = 51-95) and follow-up 75 months (IQR = 35-115). Late surgery correlated with disease progression before surgery (0.34% versus 1.54%; OR = 4.31; p = 0.022); larger micrometastases (1.40 mm vs. 2.95 mm; p = 0.003), and increased high-risk micrometastatic deposits >1 mm (55.2% vs. 69.1%; OR = 2.04; p = 0.014). For patients post-2016, longer wait-times correlated with poorer DSS (HR = 1.01 (1.00-1.02); p = 0.011 for diagnosis-to-SNB; and HR = 1.01 (1.00-1.02); p = 0.016 for primary excision-to-SNB). Sensitivity analyses calculated ≤68-days from diagnosis (HR = 3.17 (1.19-8.46); p = 0.021) and ≤82-days from excision (HR = 2.94 (1.10-7.87); p = 0.032) as optimal treatment thresholds.

conclusionSurgical delays correlated with harm: disease progression, increased tumour burden and worse survival. SNB should occur within 68 days from diagnosis and/or 82 days from excision biopsy.

Indexed as

MelanomaSentinel Lymph Node BiopsySkin NeoplasmsAdultAgedDisease ProgressionFemaleHumansLymphatic MetastasisMaleMiddle AgedNeoplasm MicrometastasisRetrospective StudiesTime FactorsTreatment DelayTumor Burden

Identifiers

PMID42303829
PMCPMC13534719

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.