Dual MEK/AKT inhibition with trametinib and GSK2141795 does not yield clinical benefit in metastatic NRAS-mutant and wild-type melanoma
Author:
Affiliation:
1. UCSF Melanoma Oncology; San Francisco CA USA
2. UCSF Dermatology; San Francisco CA USA
3. UCSD Dermatopathology; La Jolla CA USA
4. Memorial Sloan Kettering Cancer Center; New York NY USA
Funder
National Comprehensive Cancer Network
Publisher
Wiley
Subject
Dermatology,General Biochemistry, Genetics and Molecular Biology,Oncology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/pcmr.12644/fullpdf
Reference18 articles.
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2. MEK162 for patients with advanced melanoma harbouring NRAS or Val600 BRAF mutations: A non-randomised, open-label phase 2 study;Ascierto;The Lancet. Oncology,2013
3. A phase Ib dose-escalation study of the oral pan-PI3K inhibitor buparlisib (BKM120) in combination with the oral MEK1/2 inhibitor trametinib (GSK1120212) in patients with selected advanced solid tumors;Bedard;Clinical Cancer Research: An Official Journal of the American Association for Cancer Research,2015
4. Effect of selumetinib vs chemotherapy on progression-free survival in uveal melanoma: A randomized clinical trial;Carvajal;JAMA,2014
5. BRAF/NRAS mutation frequencies among primary tumors and metastases in patients with melanoma;Colombino;Journal of Clinical Oncology: An Official Journal of the American Society of Clinical Oncology,2012
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