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Neoadjuvant pembrolizumab, dabrafenib and trametinib in BRAFV600-mutant resectable melanoma: the randomized phase 2
Georgina V Long1,2,3,4,5, Matteo S Carlino6,7,8,9, George Au-Yeung10,11
1Melanoma Institute Australia, The University of Sydney, Sydney, New South Wales, Australia. georgina.long@sydney.edu.au.
Abstract:
Immune checkpoint inhibitors and BRAF-targeted therapy each improve survival in melanoma. Immune changes early during targeted therapy suggest the mechanisms of each drug class could work synergistically. In the non-comparative, randomized, phase 2 NeoTrio trial, we investigated whether targeted therapy could boost the proportion of patients achieving long-term recurrence-free survival with neoadjuvant immunotherapy in resectable stage III BRAFV600-mutant melanoma. Sixty patients (42% females) were randomized to pembrolizumab alone (n = 20), sequential therapy (dabrafenib plus trametinib followed by pembrolizumab; n = 20) or concurrent (triple) therapy (n = 20), followed by surgery and adjuvant therapy. The primary outcome was pathological response; secondary outcomes included radiographic response, recurrence-free survival, overall survival, surgical outcomes, peripheral blood and tumor analyses and safety. The pathological response rate was 55% (11/20; including six pathological complete responses (pCRs)) with pembrolizumab, 50% (10/20; three pCRs) with sequential therapy and 80% (16/20; ten pCRs) with concurrent therapy, which met the primary outcome in each arm. Treatment-related adverse events affected 75-100% of patients during neoadjuvant treatment, with seven early discontinuations (all in the concurrent arm). At 2 years, event-free survival was 60% with pembrolizumab, 80% with sequential therapy and 71% with concurrent therapy. Recurrences after major pathological response were more common in the targeted therapy arms, suggesting a reduction in response 'quality' when targeted therapy is added to neoadjuvant immunotherapy. Risking the curative potential of immunotherapy in melanoma cannot be justified. Pending longer follow-up, we suggest that immunotherapy and targeted therapy should not be combined in the neoadjuvant setting for melanoma. ClinicalTrials.gov registration: NCT02858921 .
Insights
Adding targeted therapy to neoadjuvant immunotherapy for melanoma did not improve long-term outcomes and may reduce response quality. Combining these treatments in the neoadjuvant setting for melanoma is not recommended.
Area of Science:
- Oncology
- Immunology
- Melanoma Research
Background:
- Immune checkpoint inhibitors and BRAF-targeted therapy are established melanoma treatments.
- Early immune changes suggest potential synergy between these therapy types.
- Neoadjuvant immunotherapy aims to improve long-term survival in resectable melanoma.
Purpose of the Study:
- To evaluate if targeted therapy enhances long-term recurrence-free survival with neoadjuvant immunotherapy.
- To assess neoadjuvant combination therapy in stage III BRAF-mutant melanoma.
- To compare pembrolizumab alone versus sequential or concurrent targeted therapy with pembrolizumab.
Main Methods:
- Phase 2 NeoTrio trial randomized 60 patients with resectable stage III BRAF-mutant melanoma.
- Treatment arms: pembrolizumab alone, sequential (dabrafenib/trametinib then pembrolizumab), or concurrent (triple) therapy.
- Outcomes included pathological response, recurrence-free survival, overall survival, and safety.
Main Results:
- Pathological response rates were 55% (pembrolizumab), 50% (sequential), and 80% (concurrent).
- Concurrent therapy met the primary outcome, but 2-year event-free survival was 60% (pembrolizumab), 80% (sequential), and 71% (concurrent).
- Higher recurrence rates observed after major pathological response in targeted therapy arms, suggesting reduced response quality.
Conclusions:
- Combining targeted therapy with neoadjuvant immunotherapy in melanoma may not improve, and could potentially reduce, response quality.
- The curative potential of immunotherapy in melanoma should not be risked by combination therapies.
- Immunotherapy and targeted therapy should not be combined in the neoadjuvant setting for melanoma pending further follow-up.
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