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Updated: Jan 3, 2026

A 3D Organotypic Melanoma Spheroid Skin Model
Published on: May 18, 2018
Adjuvant therapy for cutaneous melanoma: a systematic review and network meta-analysis of new therapies
C Longo1,2, R Pampena2, A Lallas3
1Department of Dermatology, University of Modena and Reggio Emilia, Modena, Italy.
Abstract:
New drugs have been recently approved as adjuvant therapies for melanoma. In this Bayesian network meta-analysis, we aimed to assess the best therapeutic option in terms of recurrence-free survival (RFS), overall survival (OS) and adverse events (AEs). PubMed, Embase, Cochrane library and the American Society of Clinical Oncology databases were searched from inception until 20 August 2018. We estimated adjusted hazard ratios (HRs) for RFS and OS and relative odds ratios (ORs) for AEs and surface under the cumulative ranking (SUCRA) probabilities were calculated. A number of 872 records were identified, and six were finally included in the meta-analysis. A total of 4244 patients in six studies were randomized. The following therapies were considered in the selected studies: combined dabrafenib and trametinib, vemurafenib, nivolumab, ipilimumab and pembrolizumab. Nivolumab demonstrated the highest probability (75.1%) of being the best in term of RFS, followed by dabrafenib+trametinib, pembrolizumab, ipilimumab and vemurafenib; however, OS was not estimable. Concerning AEs, pembrolizumab and nivolumab showed the highest probability to be less associated with any and 3-4 grade AEs (83.1% and 64.4%, respectively). In conclusion, all new drugs are highly effective in adjuvant setting, and the best choice is dependent of patient's context.
Insights
Nivolumab shows the highest probability for recurrence-free survival in melanoma adjuvant therapy. Pembrolizumab and nivolumab also have the highest probability for fewer adverse events, with the best choice depending on patient context.
Area of Science:
- Oncology
- Pharmacology
- Biostatistics
Background:
- Adjuvant therapy is crucial for melanoma treatment post-surgery.
- Recent approvals include novel targeted and immune therapies for melanoma.
- Comparing these new agents is essential for optimal patient outcomes.
Purpose of the Study:
- To conduct a Bayesian network meta-analysis comparing new adjuvant therapies for melanoma.
- To assess efficacy in terms of recurrence-free survival (RFS) and overall survival (OS).
- To evaluate safety profiles by analyzing adverse events (AEs).
Main Methods:
- Systematic literature search of PubMed, Embase, Cochrane Library, and ASCO databases.
- Bayesian network meta-analysis including six randomized controlled trials with 4244 patients.
- Estimation of hazard ratios (HRs) for survival and odds ratios (ORs) for AEs, with Surface Under the Cumulative Ranking (SUCRA) probabilities.
Main Results:
- Nivolumab had the highest probability (75.1%) for superior RFS, followed by dabrafenib+trametinib, pembrolizumab, ipilimumab, and vemurafenib.
- Overall survival (OS) data was not estimable across all therapies.
- Pembrolizumab and nivolumab showed the highest probability for fewer any-grade (83.1%) and grade 3-4 (64.4%) AEs, respectively.
Conclusions:
- All evaluated new adjuvant therapies demonstrate high efficacy in melanoma treatment.
- Nivolumab appears most promising for RFS, while pembrolizumab and nivolumab offer favorable safety profiles.
- The optimal therapeutic choice should be individualized based on patient-specific factors and risk tolerance.
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