Wong, Pok Fai
Wei, Wei
Gupta, Swati
Smithy, James W.
Zelterman, Daniel
Kluger, Harriet M.
Rimm, David L. https://orcid.org/0000-0001-5820-4397
Funding for this research was provided by:
Gruber Foundation
National Cancer Institute (P50CA196530)
National Cancer Institute (P30CA016359)
Navigate BioPharma
National Institutes of Health (R01 CA227473)
National Institutes of Health (K24CA172123)
National Institutes of Health (P50 CA121974)
Article History
Received: 21 January 2019
Accepted: 11 July 2019
First Online: 23 July 2019
Ethics approval and consent to participate
: The study was approved by the Yale Human Investigation Committee protocol #9505008219 and conducted in accordance with the Declaration of Helsinki. All patients provided written informed consent or waiver of consent in circumstances stipulated by the HIC protocol.
: Not applicable.
: D.L. Rimm has served as a consultant, advisor or served on a Scientific Advisory Board for Amgen, Astra Zeneca, Agendia, Biocept, Bristol-Meyers Squibb, Cell Signaling Technology, Cepheid, Daiichi Sankyo, GSK, Merck, NanoString, PerkinElmer, PAIGE, and Ultivue. He has received research funding from Astra Zeneca, Cepheid, Navigate/Novartis, NextCure, Lilly, Ultivue, and PerkinElmer. H.M. Kluger has served as a consultant for Corvus, Nektar, Biodesix, Genentech, Pfizer, Merck and Celldex, and has received research support from Merck, Apexigen and Bristol-Meyers Squibb. All other authors have no competing interests.