R
Romel Somwar
Researcher at Memorial Sloan Kettering Cancer Center
Publications - 83
Citations - 8698
Romel Somwar is an academic researcher from Memorial Sloan Kettering Cancer Center. The author has contributed to research in topics: Cancer & Medicine. The author has an hindex of 32, co-authored 62 publications receiving 7607 citations.
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Journal ArticleDOI
Acquired Resistance of Lung Adenocarcinomas to Gefitinib or Erlotinib Is Associated with a Second Mutation in the EGFR Kinase Domain
William Pao,Vincent A. Miller,Katerina Politi,Gregory J. Riely,Romel Somwar,Maureen F. Zakowski,Mark G. Kris,Harold E. Varmus +7 more
TL;DR: Biochemical analyses of transfected cells and growth inhibition studies with lung cancer cell lines demonstrate that the T790M mutation confers resistance to EGFR mutants usually sensitive to either gefitinib or erlotinib, which should help guide the search for more effective therapy against a specific subset of lung cancers.
Journal ArticleDOI
Novel D761Y and Common Secondary T790M Mutations in Epidermal Growth Factor Receptor–Mutant Lung Adenocarcinomas with Acquired Resistance to Kinase Inhibitors
Marissa Balak,Yixuan Gong,Gregory J. Riely,Romel Somwar,Allan R. Li,Maureen F. Zakowski,Anne C. Chiang,Guangli Yang,Ouathek Ouerfelli,Mark G. Kris,Marc Ladanyi,Vincent A. Miller,William Pao +12 more
TL;DR: The data suggest that the type and nature of kinase inhibitor resistance mutations may be influenced by both anatomic site and mode of binding to the kinase target.
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Optimization of Dosing for EGFR-Mutant Non–Small Cell Lung Cancer with Evolutionary Cancer Modeling
Juliann Chmielecki,Jasmine Foo,Geoffrey R. Oxnard,Katherine E. Hutchinson,Kadoaki Ohashi,Romel Somwar,Lu Wang,Katherine R. Amato,Maria E. Arcila,Martin L. Sos,Nicholas D. Socci,Agnes Viale,Elisa de Stanchina,Michelle S. Ginsberg,Roman K. Thomas,Mark G. Kris,Akira Inoue,Marc Ladanyi,Vincent A. Miller,Franziska Michor,William Pao +20 more
TL;DR: Predictive models of EGFR-mutant tumor behavior point to alternative drug dosing strategies to prevent and treat acquired resistance, and individual models based on the characteristics of diverse cancer cell types could offer clues for designing optimal treatment strategies.
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Cabozantinib in patients with advanced RET-rearranged non-small-cell lung cancer: an open-label, single-centre, phase 2, single-arm trial
Alexander Drilon,Natasha Rekhtman,Maria E. Arcila,Lu Wang,Andy Ni,Melanie Albano,Martine van Voorthuysen,Romel Somwar,Roger S. Smith,Joseph Montecalvo,Andrew J. Plodkowski,Michelle S. Ginsberg,Gregory J. Riely,Charles M. Rudin,Marc Ladanyi,Mark G. Kris +15 more
TL;DR: The study met its primary endpoint, with confirmed partial responses seen in seven of 25 response-assessable patients, and defined RET rearrangements as actionable drivers in patients with lung cancers.
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Globular adiponectin increases GLUT4 translocation and glucose uptake but reduces glycogen synthesis in rat skeletal muscle cells.
TL;DR: The present study is the first to show that globular adiponectin increases glucose uptake in skeletal muscle cells via GLUT4 translocation and subsequently reduces the rate of glycogen synthesis and shifts glucose metabolism toward lactate production.