Improved antitumor activity of immunotherapy with BRAF and MEK inhibitors in BRAF V600E melanoma
University of California, Los Angeles · Instituto de Salud Carlos III · +4 more institutions
Abstract
Combining immunotherapy and BRAF targeted therapy may result in improved antitumor activity with the high response rates of targeted therapy and the durability of responses with immunotherapy. However, the first clinical trial testing the combination of the BRAF inhibitor vemurafenib and the CTLA4 antibody ipilimumab was terminated early because of substantial liver toxicities. MEK [MAPK (mitogen-activated protein kinase) kinase] inhibitors can potentiate the MAPK inhibition in BRAF mutant cells while potentially alleviating the unwanted paradoxical MAPK activation in BRAF wild-type cells that lead to side effects when using BRAF inhibitors alone. However, there is the concern of MEK inhibitors being…
Citation impact
- FWCI
- 26.65
- Percentile
- 100%
- References
- 44
Authors
11- SHSiwen Hu‐Lieskovan
University of California, Los Angeles
- SMStephen Mok
University of California, Los Angeles
- BHBlanca Homet Moreno
University of California, Los Angeles, Instituto de Salud Carlos III, Universidad Carlos III de Madrid
- JTJennifer Tsoi
Institute for Molecular Medicine
- LRLídia Robert
University of California, Los Angeles
Topics & keywords
- Melanoma
- Immunotherapy
- Cancer research
- Medicine
- Vemurafenib
- Metastatic melanoma
- Cancer
- Internal medicine
Funding
- ACAmerican Cancer SocietyAward: RSG-12-257-01-TBE
- CCConquer Cancer Foundation
- CFConcern Foundation
- MRMelanoma Research AllianceAward: 20120279
- ASAmerican Society of Clinical Oncology
- TCTower Cancer Research Foundation
- SESociedad Española de Oncología Médica
- NINational Institutes of HealthAwards: CA086306, T32-CA009120, R21 CA169993, P50 CA086306, CA-16042, T32 CA09297, UL1TR000124, P01 CA168585, AI-28697
- CFCenter for AIDS Research, University of Washington
- NCNational Cancer InstituteAwards: P50 CA086306, CA-16042, R21 CA169993, P01 CA168585, AI-28697, UL1TR000124
- NCNational Center for Advancing Translational SciencesAward: UL1TR000124
- JCJonsson Comprehensive Cancer CenterAward: UL1TR000124
- DGDavid Geffen School of Medicine, University of California, Los AngelesAward: UL1TR000124
- CAClinical and Translational Science Institute, University of California, Los AngelesAward: UL1TR000124
- UAUCLA AIDS Institute