3
UK pathway Β· Step 3 of 6

Staging

AJCC 8 melanoma, BWH for cSCC, AJCC 8 dedicated systems for MCC, conjunctival and Merkel. Imaging thresholds, SLNB indications, perineural-spread workup, and the pre-MDT data that determine treatment selection.

Melanoma β€” AJCC 8

AJCC 8 (Gershenwald 2017, in force from 2018) is the UK standard. Use the interactive melanoma staging calculator to map a Breslow / ulceration / mitotic / SLNB combination to the stage group.

T-category

TBreslowa/b qualifier
T1< 0.8 mm (no ulceration); or < 1.0 mm with ulceration; or 0.8–1.0 mm anyT1a / T1b β€” note AJCC 8 redrew the boundary at 0.8 mm
T21.01–2.0 mmT2a no ulceration Β· T2b ulcerated
T32.01–4.0 mmT3a / T3b
T4> 4.0 mmT4a / T4b

Mitotic rate is reported in the RCPath dataset but is no longer a determinant of T1a vs T1b in AJCC 8 β€” that was an AJCC 7 rule.

N-category

The N1c trap: in-transit, satellite or microsatellite metastases ONLY (no involved regional nodes) = N1c. Add one node β†’ N2c. β‰₯ 2 nodes or matted + in-transit / satellite / microsatellite β†’ N3c.

M-category

M1a distant skin / soft tissue / non-regional nodes Β· M1b lung Β· M1c other non-CNS visceral Β· M1d CNS. Each is further qualified by LDH (0 = normal; 1 = elevated). AJCC 8 added M1d as a separate sub-category, reflecting the prognostic weight of brain disease.

cSCC β€” BWH first, AJCC 8 for H&N

BAD 2020 recommends the Brigham & Women's (BWH) T-stage in preference to AJCC 8 for cSCC β€” it outperforms AJCC 8 for prognostic discrimination in most cohorts. Use the on-site BWH staging calculator.

BWHRisk factorsNodal metastasisDeath
T10< 1%β‰ˆ 0%
T2a1~ 5%~ 1%
T2b2–3~ 20%~ 10%
T34 (or bone invasion)> 50%> 30%

BWH counts four high-risk factors: diameter β‰₯ 2 cm, poor differentiation, PNI of a nerve β‰₯ 0.1 mm calibre, and invasion beyond subcutaneous fat (excluding bone). Bone invasion is automatic T3. For head & neck cSCC, the AJCC 8 dedicated chapter is also used by many MDTs β€” its T-criteria incorporate size, depth > 6 mm, PNI of a named nerve, and bone erosion.

PNI sub-criteria

Any ONE of: nerve calibre β‰₯ 0.1 mm; PNI deeper than dermis; PNI of a named nerve. Single small-calibre dermal-twig PNI alone does not qualify as high-risk PNI.

BCC β€” staging is rarely formal

BCC almost never metastasises; formal staging is reserved for locally advanced or rare metastatic BCC requiring imaging. Subtype (low- vs high-risk histology β€” morphoeic / infiltrative / micronodular / basosquamous), depth and margins drive management decisions.

Merkel cell carcinoma

AJCC 8 MCC chapter. Localised disease (clinically node-negative) requires SLNB at the time of WLE for accurate staging β€” occult nodal involvement is common in MCC. PET-CT is standard at baseline per the EADO 2022 consensus to detect occult distant disease.

Conjunctival melanoma

Has its own AJCC 8 chapter β€” distinct from cutaneous and uveal melanoma. Managed by ocular oncology / oculoplastic surgery.

SLNB indications (melanoma β€” NICE NG14 Β§1.4.3–4)

  • Do not offer SLNB for stage IA melanoma.
  • Consider SLNB for Breslow 0.8–1.0 mm melanoma with ulceration, lymphovascular invasion or mitotic index of 2/mmΒ² or more, after discussion of benefits, risks and uncertainty.
  • Consider SLNB for Breslow > 1.0 mm melanoma after discussion of benefits, risks and uncertainty; this includes T2b and thicker tumours, but NG14 frames the decision as shared consideration rather than an automatic rule.
  • SLN status changes stage (any involved SLN = at least N1a; stage III) and triggers adjuvant ICI / BRAF/MEK discussions per the relevant NICE TAs.
  • Completion lymphadenectomy after SLN+ is no longer standard in most patients (MSLT-II: no OS benefit). Observation + adjuvant ICI is the modern UK default; lymphadenectomy is reserved for selected high-burden / extracapsular cases at MDT.
Practical. SLNB is performed at the same operation as WLE β€” needs lymphoscintigraphy with 99mTc-nanocolloid pre-operatively (sometimes the day before) plus patent blue dye at induction. Plan logistics with nuclear medicine early; multiple basins are common in head/neck and trunk lesions and need pre-operative lymphoscintigraphy.

Imaging β€” what to ask for, when

IndicationModalityNotes
Stage 0–IIA melanoma, asymptomaticNo routine imagingPer NICE NG14.
Stage IIB+ melanoma, baselineCT TAP Β± MRI brainPer NG14 + local MDT protocol.
Stage III/IV melanomaCT TAP + MRI brainBrain MRI more sensitive than CT for melanoma metastases.
cSCC with named-nerve PNIMRI head/neck with gadolinium + fat-saturationThe standard for perineural spread workup. Specifically request review of the relevant nerve tract.
High-risk cSCC (BWH T2b/T3)USS regional nodes Β± CTUSS is high-sensitivity for nodal disease.
Merkel cell carcinomaPET-CT at baseline Β± MRI brainEADO consensus.
Suspected mucosal / uveal melanomaSite-specific imagingCoordinate with ocular oncology / H&N team.
Adnexal carcinoma with high-risk featuresCT TAP per MDTHidradenocarcinoma, porocarcinoma, MAC etc.

Pre-MDT package

By the time a case reaches MDT, you ideally have:

  • Confirmed histology with RCPath-dataset reporting
  • BWH / AJCC stage with the working calculator output
  • Imaging where indicated, with formal report
  • SLNB result if performed
  • BRAF / MMR / MCPyV ancillary results as relevant
  • Patient performance status, comorbidity profile, immunosuppression status, prior radiotherapy / treatment
  • Patient preferences and family / social context β€” pertinent to surgical fitness and reconstruction decisions

Source basis

  1. This page was launch-reviewed on 19 May 2026. See the source-control register for the NICE, NHS England, BAD, RCPath, WHO, AJCC / TNM and pivotal-trial sources used across the site; check live guidance and local MDT policy before applying recommendations.

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