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Updated: Dec 31, 2025

A 3D Organotypic Melanoma Spheroid Skin Model
Published on: May 18, 2018
Thick melanomas without lymph node metastases: A forgotten group with poor prognosis
M A El Sharouni1, A J Witkamp2, V Sigurdsson1
1Department of Dermatology, University Medical Center Utrecht, Utrecht University, PO Box 85500 3508, GA, Utrecht, the Netherlands.
Thick melanomas without lymph node metastases (pN-) have a poor prognosis, similar to thinner melanomas with metastases (pN+). These high-risk pN- patients should be considered for adjuvant trials.
Area of Science:
- Oncology
- Dermatology
- Surgical Pathology
Background:
- Adjuvant therapy is available for melanoma patients with sentinel lymph node (SLN) metastases (pN+).
- However, no adjuvant therapy is established for thick melanomas without SLN involvement (pN-).
Purpose of the Study:
- To assess overall survival (OS) and relative survival (RS) in patients with thick melanomas (>4.0 mm Breslow thickness [BT]) who are either pN- or pN+.
- To compare survival outcomes between thick pN- melanomas and thinner melanomas with positive SLN status (≤4.0 mm pN+).
Main Methods:
- Retrieved clinicopathological data from a Dutch cohort of thick and/or pN+ melanoma patients (2000-2014).
- Compared OS and RS using Kaplan-Meier curves.
- Developed a Cox-regression model to identify OS determinants in >4.0 mm pN- patients.
Main Results:
- In 54,645 patients, 7.2% had >4.0 mm thick melanomas.
- Five-year OS was 70.5% for >4.0 mm pN- and 48.1% for >4.0 mm pN+ melanomas (p < 0.001).
- Five-year OS for ≤4.0 mm pN+ patients (71.5%) was comparable to >4.0 mm pN- patients (p = 0.24).
- Higher age, increased BT, ulceration, and male gender were associated with poor survival in >4.0 mm pN- patients.
Conclusions:
- Thick melanomas without lymph node metastases (pN-) exhibit a poor prognosis, comparable to thinner melanomas with positive lymph node status (pN+).
- Current melanoma treatment guidelines do not adequately account for the high-risk nature of thick pN- melanomas.
- These high-risk patients warrant inclusion in future adjuvant clinical trials.
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