A plain language summary of the 5-year update from part 1 of the COLUMBUS study: encorafenib and binimetinib for people with BRAF V600-mutant melanoma
Abstract
What is this summary about?
Here, we summarize the 5-year results from part 1 of the COLUMBUS clinical study, which looked at the combination treatment of encorafenib plus binimetinib in people with a specific type of skin cancer called melanoma. Encorafenib (BRAFTOVI®) and binimetinib (MEKTOVI®) are medicines used to treat a type of melanoma that has a change in the BRAF gene, called advanced or metastatic BRAF V600-mutant melanoma.
Participants with advanced or metastatic BRAF V600-mutant melanoma took either encorafenib plus binimetinib together (COMBO group), compared with encorafenib alone (ENCO group) or vemurafenib (ZELBORAF®) alone (VEMU group).
What were the results?
In this 5-year update, more participants in the COMBO group were alive for longer without their disease getting worse after 5 years than those in the VEMU and ENCO groups. Patients in the COMBO group were alive for longer without their disease getting worse when they:
Had less advanced cancer
Were able to do more daily activities
Had normal lactate dehydrogenase (LDH) levels
Had fewer organs with tumors before treatment
After treatment, fewer participants in the COMBO group received additional anticancer treatment than participants in the VEMU and ENCO groups. The number of participants who reported severe side effects was similar for each treatment. The side effects caused by the drugs in the COMBO group decreased over time.
What do the results mean?
Overall, this 5-year update confirmed that people with BRAF V600-mutant melanoma that has spread to other parts of the body and who took encorafenib plus binimetinib were alive for longer without their disease getting worse than those who took vemurafenib or encorafenib alone.
Clinical Trial Registration:NCT01909453 (ClinicalTrials.gov)
This is an abstract of the Plain Language Summary of Publication article.
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Link to original article here
Acknowledgments
Pfizer would like to thank the participants and their families for participating in this study, as well as the investigators and the clinical teams for making this study possible.
Financial & competing interests disclosure
Full author disclosure information can be found in the original article in the Journal of Clinical Oncology.
Writing support was provided by Blaise Low, PhD, at MediTech Media, Nucleus Global, and was funded by Pfizer.
Open access
This work is licensed under the Attribution-NonCommercial-NoDerivatives 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/