Genetic Prostate Cancer Studies Are Needed to Push the Needle Forward

Commentary
Video

Robust genetic testing guidelines in the prostate cancer space must be supported by strong clinical research before they can be properly implemented, says William J. Catalona, MD.

Research into genetic testing as a tool for localized diagnosis is still in its early days across most cancer types, and prostate cancer is no exception, according to William J. Catalona, MD.

In a conversation with CancerNetwork® during the 2023 Society of Urologic Oncology (SUO) Annual Meeting, Catalona, a professor of urology at the Feinberg School of Medicine, Northwestern University, emphasized the necessity of conducting additional genetic studies in the prostate cancer space to collect firm evidence. From there, robust guidelines can be drafted and implemented.

Transcript:

We're relatively early in the phase of genetic studies of prostate cancer. Many of [our] colleagues may not be as familiar with all of the latest developments if their area is focused in, say, radiation therapy, medical oncology, or other areas. Hopefully, they [have] learned a little something about what's current in the genetics of prostate cancer [from my presentation]. The other thing is that we really need to [base] our clinical guidelines for managing patients on firm scientific evidence. Without the genetic research, that firm scientific evidence is not there. Once we have the firm scientific evidence, then we have robust guidelines. But then we have to move beyond the robust guidelines into a field called implementation science, where we have to persuade the doctors and patients out there to do the right thing because there's good scientific evidence to support adopting these guidelines.

Reference

Catalona WJ. Localized diagnosis: genetic testing. 2023 Society of Urologic Oncology (SUO) Annual Meeting; November 28-December 1, 2023; Washington, DC.

Recent Videos
Thomas Powles, MBBS, MRCP, MD, highlighted fatigue, nausea, and peripheral neuropathy as toxicities observed with enfortumab vedotin plus pembrolizumab.
Large international meetings may facilitate conversations regarding disparities of care outside of high-income countries.
Updated findings from the phase 3 EV-302 trial show enduring responses and survival improvements with enfortumab vedotin plus pembrolizumab.
AI-powered tools may help alleviate doctor burnout and give clinicians more time to directly engage with patients.
Artificial intelligence may have the potential to enrich pathology practices to help identify aspects of tumor biology not seen with the human eye.
Efficacy results from the MASAI trial preceded the creation of the UK-funded EDITH trial, assessing 5 AI platforms in 700,000 women undergoing mammography.
Related Content