Genomic drivers of resistance to ar therapies

Genomic drivers of resistance to ar therapies


Play all audios:


Access through your institution Buy or subscribe Researchers in Canada have identified genomic drivers of resistance to androgen-receptor (AR)-directed therapies in men with metastatic


castration-resistant prostate cancer (mCRPC). Annala _ et al_. performed whole-exome and/or deep targeted sequencing of plasma-derived cell-free DNA samples from 202 treatment-naive men with


mCRPC randomly assigned to abiraterone or enzalutamide. Defects in _BRCA2_ and _ATM_ were associated with poor clinical outcomes independently of clinical prognostic factors and abundance


of circulating tumour DNA. Deleterious alterations in _TP53_ were also associated with reduced time to progression. This is a preview of subscription content, access via your institution


ACCESS OPTIONS Access through your institution Access Nature and 54 other Nature Portfolio journals Get Nature+, our best-value online-access subscription $29.99 / 30 days cancel any time


Learn more Subscribe to this journal Receive 12 print issues and online access $209.00 per year only $17.42 per issue Learn more Buy this article * Purchase on SpringerLink * Instant access


to full article PDF Buy now Prices may be subject to local taxes which are calculated during checkout ADDITIONAL ACCESS OPTIONS: * Log in * Learn about institutional subscriptions * Read our


FAQs * Contact customer support REFERENCES * Annala, M. _ et al_. Circulating tumor DNA genomics correlate with resistance to abiraterone and enzalutamide in prostate cancer. _Cancer


Discov._ https://doi.org/10.1158/2159-8290.CD-17-0937 (2018) Article  CAS  Google Scholar  Download references Authors * Rebecca Kelsey View author publications You can also search for this


author inPubMed Google Scholar RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Kelsey, R. Genomic drivers of resistance to AR therapies. _Nat Rev Urol_


15, 202 (2018). https://doi.org/10.1038/nrurol.2018.18 Download citation * Published: 13 February 2018 * Issue Date: April 2018 * DOI: https://doi.org/10.1038/nrurol.2018.18 SHARE THIS


ARTICLE Anyone you share the following link with will be able to read this content: Get shareable link Sorry, a shareable link is not currently available for this article. Copy to clipboard


Provided by the Springer Nature SharedIt content-sharing initiative