What is the appropriate management for a patient with nodular malignant melanoma, 2.9 mm thick, with ulceration, mitotic index of 5/mm^2, and pathologic stage pT3b, showing pleomorphic melanocytes, expansile dermal growth, and tumor-infiltrating lymphocytes, with limited focus suspicious for lymphovascular involvement?

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Last updated: January 31, 2026View editorial policy

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Management of pT3b Nodular Melanoma (2.9 mm, Ulcerated)

This patient requires wide local excision with 2 cm margins and sentinel lymph node biopsy (SLNB), followed by consideration for adjuvant immunotherapy if the sentinel node is positive. 1, 2

Immediate Surgical Management

Wide Local Excision

  • Perform wide excision with 2 cm surgical margins for this melanoma >2 mm in Breslow thickness 1
  • The 2 cm margin recommendation is based on Level II evidence from randomized trials showing equivalent survival with reduced morbidity compared to wider margins 1, 3
  • Margins may need modification only if the lesion involves functionally critical areas (fingers, toes, face, ear), which does not appear to be the case here 1

Sentinel Lymph Node Biopsy (SLNB)

  • SLNB is mandatory for this patient given the tumor thickness of 2.9 mm, which carries approximately 20% risk of sentinel node positivity 2, 4
  • The presence of ulceration, mitotic index of 5/mm², and suspicious lymphovascular involvement further increases the likelihood of nodal metastases 4, 5
  • SLNB should be performed simultaneously with the wide excision to avoid alterations in lymphatic drainage patterns 2, 3
  • This procedure must be performed at an experienced center with skilled teams 1, 2

Critical point: The suspicious lymphovascular invasion noted on pathology is a particularly strong predictor of sentinel node positivity—second only to tumor thickness itself on multivariate analysis 5

What NOT to Do

  • Do not perform elective complete lymph node dissection without first confirming sentinel node status, as prophylactic lymphadenectomy provides no survival benefit and causes significant morbidity 1, 3
  • Do not perform prophylactic lymph node irradiation, as this is not recommended 1

Staging Workup

Imaging Recommendations

  • Cross-sectional imaging (CT chest/abdomen/pelvis or PET-CT) is recommended for this stage IIB/III melanoma to evaluate for distant metastases 1, 6, 2
  • PET-CT is specifically indicated for melanomas ≥4 mm or stage IIB-IIC and higher to evaluate for distant disease 6, 2
  • While this patient's primary is 2.9 mm, the pT3b classification with ulceration, high mitotic rate, and suspicious lymphovascular involvement warrants baseline imaging 6

Laboratory Studies

  • Obtain baseline LDH, complete blood count, and liver function tests 1
  • Elevated LDH is an important prognostic marker for metastatic disease 1

Adjuvant Therapy Considerations

If Sentinel Node is Positive (Stage III Disease)

  • Adjuvant immunotherapy with pembrolizumab or nivolumab should be strongly considered for completely resected stage III melanoma 7, 8
  • Pembrolizumab 200 mg IV every 3 weeks for up to 1 year demonstrated statistically significant improvement in recurrence-free survival in the KEYNOTE-054 trial for stage III disease 7
  • Nivolumab 480 mg IV every 4 weeks (or 240 mg every 2 weeks) for up to 1 year showed superior recurrence-free survival compared to ipilimumab 10 mg/kg in the CHECKMATE-238 trial 8

If Sentinel Node is Negative (Stage IIB Disease)

  • Adjuvant immunotherapy should still be considered given the high-risk features 7, 8
  • Pembrolizumab demonstrated significant improvement in recurrence-free survival for stage IIB/IIC melanoma in the KEYNOTE-716 trial 7
  • Nivolumab showed significant improvement in recurrence-free survival for stage IIB/IIC melanoma in the CHECKMATE-76K trial 8

High-Risk Pathologic Features in This Case

Several features in this pathology report warrant particular attention:

  • Ulceration: Major adverse prognostic factor that upstages the tumor from pT3a to pT3b 1, 9
  • Mitotic index of 5/mm²: Independently predicts melanoma-specific survival and should influence adjuvant therapy decisions 9, 5
  • Suspicious lymphovascular invasion: Second strongest predictor of sentinel node positivity after tumor thickness 5
  • Brisk tumor-infiltrating lymphocytes: Generally a favorable prognostic sign, though does not negate the need for standard management 9, 10

Common Pitfalls to Avoid

  • Do not delay SLNB: Must be performed before or simultaneously with wide excision, not as a delayed procedure 2, 3
  • Do not assume negative nodes based on favorable features: Despite brisk TILs and absence of microsatellitosis, the combination of thickness, ulceration, and suspicious LVI mandates SLNB 4, 5
  • Do not use PET-CT as a substitute for SLNB: PET-CT has very low yield for detecting microscopic nodal disease and cannot replace SLNB for staging 6, 2

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Sentinel Lymph Node Biopsy for Back Melanoma

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Treatment of Melanoma with Breslow Thickness 1-2 mm

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Utilizzo della PET-TAC nel Melanoma

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Melanoma pathology reporting and staging.

Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 2020

Research

Pathology of Melanoma.

The Surgical clinics of North America, 2020

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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