Lung Master Protocol (Lung-MAP)—A Biomarker-Driven Protocol for Accelerating Development of Therapies for Squamous Cell Lung Cancer: SWOG S1400

Roy S. Herbst(Yale Cancer Center), David R. Gandara(University of California Davis Medical Center), Fred R. Hirsch(University of Colorado Hospital), Mary W. Redman(Fred Hutch Cancer Center), Michael LeBlanc(Fred Hutch Cancer Center), Philip C. Mack(University of California Davis Medical Center), Lawrence H. Schwartz(Columbia University Irving Medical Center), Everett E. Vokes(University of Illinois Chicago), Suresh S. Ramalingam(Emory University), Jeffrey D. Bradley(Washington University in St. Louis), Dana B. Sparks(SWOG Cancer Research Network), Yang Zhou(Yale Cancer Center), Crystal Miwa(SWOG Cancer Research Network), Vincent A. Miller(GlobalFoundries (United States)), Roman Yelensky(GlobalFoundries (United States)), Yali Li(GlobalFoundries (United States)), Jeff Allen(Friends of Cancer Research), Ellen V. Sigal(Friends of Cancer Research), David Wholley(Foundation for the National Institutes of Health), Caroline C. Sigman(CCS Associates (United States)), Gideon M. Blumenthal(Center for Drug Evaluation and Research), Shakun Malik(National Cancer Institute), Gary J. Kelloff(National Cancer Institute), Jeffrey S. Abrams(National Cancer Institute), Charles D. Blanke(Oregon Health & Science University), Vassiliki A. Papadimitrakopoulou(The University of Texas MD Anderson Cancer Center)
Clinical Cancer Research
February 14, 2015
Cited by 239Open Access
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Abstract

The Lung Master Protocol (Lung-MAP, S1400) is a groundbreaking clinical trial designed to advance the efficient development of targeted therapies for squamous cell carcinoma (SCC) of the lung. There are no approved targeted therapies specific to advanced lung SCC, although The Cancer Genome Atlas project and similar studies have detected a significant number of somatic gene mutations/amplifications in lung SCC, some of which are targetable by investigational agents. However, the frequency of these changes is low (5%-20%), making recruitment and study conduct challenging in the traditional clinical trial setting. Here, we describe our approach to development of a biomarker-driven phase II/II multisubstudy "Master Protocol," using a common platform (next-generation DNA sequencing) to identify actionable molecular abnormalities, followed by randomization to the relevant targeted therapy versus standard of care.


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