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.

The Journal of Dermatology
|November 12, 2020
PubMed

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.

Related Concept Videos

Combination Therapies and Personalized Medicine02:50

Combination Therapies and Personalized Medicine

Combining two or more treatment methods increases the life span of cancer patients while reducing damage to vital organs or tissue from the overuse of a single treatment. Combination therapy also targets different cancer-inducing pathways, thus reducing the chances of developing resistance to treatment.
The combination of the drug acetazolamide and sulforaphane is a good example of combination therapy to treat cancer. The cells in the interior of a large tumor often die due to the hypoxic and...
5.6K
Targeted Cancer Therapies02:57

Targeted Cancer Therapies

The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against...
8.2K
Treatment Resistant Cancers02:56

Treatment Resistant Cancers

Cancer is the second leading cause of death in the United States. A cancer cell is genetically unstable and hence can mutate faster. They can also modify their microenvironment and escape immune surveillance. The difficulties in treating cancer are further compounded by the emergence of rapid resistance to anticancer drugs. The most common ways to attain resistance in cancer cells include alteration in drug transport and metabolism, modification of drug target, elevated DNA damage response, or...
3.5K