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dc.date.accessioned2022-12-13T18:24:03Z
dc.date.available2022-12-13T18:24:03Z
dc.date.issued2022
dc.identifier.urihttps://hdl.handle.net/1721.1/146862
dc.description.abstractMolecular profiling studies have enabled discoveries for metastatic prostate cancer (MPC) but have predominantly occurred in academic medical institutions and involved non-representative patient populations. We established the Metastatic Prostate Cancer Project (MPCproject, mpcproject.org), a patient-partnered initiative to involve patients with MPC living anywhere in the US and Canada in molecular research. Here, we present results from our partnership with the first 706 MPCproject participants. While 41% of patient partners live in rural, physician-shortage, or medically underserved areas, the MPCproject has not yet achieved racial diversity, a disparity that demands new initiatives detailed herein. Among molecular data from 333 patient partners (572 samples), exome sequencing of 63 tumor and 19 cell-free DNA (cfDNA) samples recapitulated known findings in MPC, while inexpensive ultra-low-coverage sequencing of 318 cfDNA samples revealed clinically relevant AR amplifications. This study illustrates the power of a growing, longitudinal partnership with patients to generate a more representative understanding of MPC.en_US
dc.language.isoen
dc.publisherElsevier BVen_US
dc.relation.isversionof10.1016/J.XGEN.2022.100169en_US
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourceElsevieren_US
dc.titleA patient-driven clinicogenomic partnership for metastatic prostate canceren_US
dc.typeArticleen_US
dc.identifier.citation2022. "A patient-driven clinicogenomic partnership for metastatic prostate cancer." Cell Genomics, 2 (9).
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.relation.journalCell Genomicsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2022-12-13T17:08:59Z
dspace.orderedauthorsCrowdis, J; Balch, S; Sterlin, L; Thomas, BS; Camp, SY; Dunphy, M; Anastasio, E; Shah, S; Damon, AL; Ramos, R; Sosa, DM; Small, IK; Tomson, BN; Nguyen, CM; McGillicuddy, M; Chastain, PS; He, MX; Cheung, ATM; Wankowicz, S; Tewari, AK; Kim, D; AlDubayan, SH; Dowdye, A; Zola, B; Nowak, J; Manarite, J; Gunn, IH; Olson, B; Lander, ES; Painter, CA; Wagle, N; Van Allen, EMen_US
dspace.date.submission2022-12-13T17:09:01Z
mit.journal.volume2en_US
mit.journal.issue9en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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