| Literature DB >> 28331002 |
Chantal Pauli1,2,3, Benjamin D Hopkins4, Davide Prandi5, Reid Shaw6, Tarcisio Fedrizzi5, Andrea Sboner1,4,7, Verena Sailer1,2, Michael Augello1,4, Loredana Puca1, Rachele Rosati6, Terra J McNary1, Yelena Churakova1, Cynthia Cheung1, Joanna Triscott1, David Pisapia1,2, Rema Rao1,2, Juan Miguel Mosquera1,2, Brian Robinson1,2, Bishoy M Faltas1,8, Brooke E Emerling4, Vijayakrishna K Gadi9, Brady Bernard6, Olivier Elemento1,4,7, Himisha Beltran1,8, Francesca Demichelis1,5, Christopher J Kemp10, Carla Grandori6, Lewis C Cantley4, Mark A Rubin11,2,4.
Abstract
Precision medicine is an approach that takes into account the influence of individuals' genes, environment, and lifestyle exposures to tailor interventions. Here, we describe the development of a robust precision cancer care platform that integrates whole-exome sequencing with a living biobank that enables high-throughput drug screens on patient-derived tumor organoids. To date, 56 tumor-derived organoid cultures and 19 patient-derived xenograft (PDX) models have been established from the 769 patients enrolled in an Institutional Review Board-approved clinical trial. Because genomics alone was insufficient to identify therapeutic options for the majority of patients with advanced disease, we used high-throughput drug screening to discover effective treatment strategies. Analysis of tumor-derived cells from four cases, two uterine malignancies and two colon cancers, identified effective drugs and drug combinations that were subsequently validated using 3-D cultures and PDX models. This platform thereby promotes the discovery of novel therapeutic approaches that can be assessed in clinical trials and provides personalized therapeutic options for individual patients where standard clinical options have been exhausted.Significance: Integration of genomic data with drug screening from personalized in vitro and in vivo cancer models guides precision cancer care and fuels next-generation research. Cancer Discov; 7(5); 462-77. ©2017 AACR.See related commentary by Picco and Garnett, p. 456This article is highlighted in the In This Issue feature, p. 443. ©2017 American Association for Cancer Research.Entities:
Mesh:
Year: 2017 PMID: 28331002 PMCID: PMC5413423 DOI: 10.1158/2159-8290.CD-16-1154
Source DB: PubMed Journal: Cancer Discov ISSN: 2159-8274 Impact factor: 39.397