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Meeting report

Inside prostate cancer news from the 2021 ASCO Genitourinary Cancers Symposium

, , , , , & show all
Pages 1207-1210 | Received 03 May 2021, Accepted 24 Aug 2021, Published online: 09 Sep 2021
 

ABSTRACT

Background

Prostate cancer (PC) is a heterogeneous disease that requires a personalized treatment approach for proper patient management.

Aim

We analyzed a selected overview of the most important news recently presented at the 2021 ASCO genitourinary cancer symposium.

Results

In particular, we focused on the identification of predictive biomarkers as potential targets for therapy. Molecular signatures of increased T cell activity, proliferation, and hormone dependence were associated with greater probability of response to apalutamide in non-metastatic CRPC. Pathogenic variants of DDR genes mutations detected with circulating tumor DNA (ctDNA) analysis, which had a high concordance with tumor tissue analysis, might represent a useful way for selecting mutated patients for poly (adenosine diphosphate [ADP]-ribose) polymerase (PARP) inhibitors therapy. Loss of PTEN could be a target for ipatasertib (a pan-AKT inhibitor) associated with abiraterone in mCRPC patients.

Conclusions

The 2021 ASCO Genitourinary Cancers Symposium significantly contributed to the complex research goal of intimately understanding PC carcinogenesis with the ultimate aim of improving patient outcomes.

Declaration of interest

R. Lacovelli has served as an advisory board member for Pfizer, Janssen, Sanofi, IPSEN, MSD, Novartis. G. Tortora has served as an advisory board member for BMS and Novartis. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.

Reviewer disclosures

Peer reviewers on this manuscript have no relevant financial or other relationships to disclose.

Additional information

Funding

This paper received no funding.

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