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Updated: Nov 30, 2025

Screening for Melanoma Modifiers using a Zebrafish Autochthonous Tumor Model
Published on: November 13, 2012
Case series of BRAF-mutated advanced melanoma treated with encorafenib plus binimetinib combination therapy
Taku Fujimura1, Koji Yoshino2, Hiroshi Kato3
1Department of Dermatology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Abstract:
The efficacy of encorafenib plus binimetinib (E + B) combination therapy for BRAF-mutated advanced melanoma as second-line therapy and beyond is still unknown. In this report, we investigated 22 cases of BRAF-mutated advanced melanoma treated with E + B combination therapy. The objective response rate (ORR) for the total cohort was 68.4%. Notably, the ORR for the second-line and beyond cohort was 73.3%, suggesting that the therapeutic effect of E + B combination therapy is comparable with that of first-line targeted therapy. In contrast, overall survival and progress-free survival in our present cohort was worse than that in a previous clinical trial. Notably, although the incidence rate of severe adverse events was higher than that in a previous report, our present study suggested that E + B combination therapy is a well-tolerated antimelanoma regimen. Our present study suggested that the efficacy and safety profile of E + B combination therapy as a second-line therapy and beyond is comparable with that of first-line targeted therapy.
Insights
Encorafenib plus binimetinib (E+B) shows a 73.3% objective response rate in advanced BRAF-mutated melanoma as second-line treatment. This combination therapy is well-tolerated and comparable to first-line treatments.
Area of Science:
- Oncology
- Dermatology
- Pharmacology
Background:
- Advanced melanoma with BRAF mutations presents treatment challenges.
- The efficacy of encorafenib plus binimetinib (E+B) as second-line therapy is not well-established.
- Understanding treatment outcomes for E+B in later lines of therapy is crucial.
Purpose of the Study:
- To evaluate the efficacy and safety of encorafenib plus binimetinib (E+B) in patients with BRAF-mutated advanced melanoma receiving second-line or later treatment.
- To compare the objective response rate (ORR) of E+B in this cohort with first-line targeted therapy outcomes.
- To assess the safety profile and tolerability of E+B in a real-world setting.
Main Methods:
- Retrospective analysis of 22 cases of BRAF-mutated advanced melanoma treated with E+B.
- Calculation of objective response rate (ORR) for the entire cohort and the second-line and beyond subgroup.
- Evaluation of overall survival (OS) and progression-free survival (PFS).
- Assessment of severe adverse events (SAEs).
Main Results:
- The overall objective response rate (ORR) was 68.4%.
- For the second-line and beyond cohort, the ORR was 73.3%, comparable to first-line targeted therapy.
- Overall survival and progression-free survival were worse compared to a previous clinical trial.
- The incidence of severe adverse events was higher than previously reported, but E+B was deemed well-tolerated.
Conclusions:
- Encorafenib plus binimetinib (E+B) demonstrates significant efficacy as a second-line or later treatment for BRAF-mutated advanced melanoma.
- The therapeutic effect of E+B in later lines is comparable to first-line targeted therapy, with a notable ORR.
- Despite a higher incidence of severe adverse events, E+B is considered a well-tolerated regimen for advanced melanoma.
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