Accurate Risk Status Assessment Critical to Prostate Cancer Care

Gina Columbus @ginacolumbusonc
Published Online: Thursday, Aug 25, 2016

Julio Pow-Sang, MD

Julio Pow-Sang, MD

Determining whether a patient with prostate cancer has low- or intermediate-risk disease is a significant distinction to make, as the 2 subsets are managed quite differently, explains Julio Pow-Sang, MD.

In a lecture at the 2016 OncLive State of the Science Summit on Genitourinary Cancers, Pow-Sang, MD, chair of Urological Oncology at Moffitt Cancer Center, discussed the significance of assessing risk status, options for patients whose risk status falls in a “grey-zone,” and how technology is helping oncologists more accurately characterize risk. He expanded on these topics in an interview with OncLive during the meeting.

OncLive: Please provide an overview of your lecture on the options for patients with low- and intermediate-risk disease.

Pow-Sang: The goal is to clarify the distinction between risk groups with localized prostate cancer because that drives a lot of the decisions in management. One of the fortunate things happening is that, with better molecular testing and imaging, one is better able to characterize the tumors. Traditionally, cancers that were localized—specifically in prostate cancer—were divided into organ-confined cancer, localized cancer, and locally extensive cancer. That was the extent of the stratification, and it was very difficult to determine what treatment to give.

As we learned more and imaging [evolved], we were able to define better risk categories. The most traditional, modern one is the D’Amico Classification System, which divides localized cancer into low, intermediate, and high risk. When we are talking about low and intermediate risk, that classification blurs a little bit because there’s an overlap between low and intermediate groups.

More importantly, at present, one of the main options for low-risk patients is to do active surveillance. Initially, the sophistication of the testing to determine that a man was really truly a low-risk patient was very rudimentary. There was an approximate 30% chance that, with further testing, the patient was actually an intermediate-risk one. That was critical because intermediate-risk patients are more likely to have cancer spread and, eventually, die from their cancer. Therefore, they need treatment. That would be the general recommendation.

We also recognize that there is a subset of men who have cancer and are never going to have problems for the rest of their life—and they start dying from something else. Newer tests and a better understanding of the behavior of the cancer have helped us determine who those men are versus the ones who might need treatment.

What are some of the key considerations for oncologists when treating patients?

One of the most important things is to define—as best as one can with the technology available—what risk that the man really falls into. That’s going to drive the discussion about potential management options—whether active surveillance is an option or not. If one defines that the man [has] very low-risk disease, one could feel very comfortable with watching that person and explaining the reasons why.

When dealing with an intermediate-risk patient, we start moving into the area of truly intermediate, high-intermediate, or even going into the high-risk territory—in which one might have to consider clinical trials because conventional treatments are not very good, or one might try to consider more aggressive local treatments, or a combination of treatments.

You mentioned the technology that’s available today. How can this technology be improved?

We have very good technology [now] compared with what we had only 5 or 10 years ago, and it keeps improving. The big push now is to better characterize the tumors by molecular markers. There are several available. There are sets of genes that one can test for and then better determine the behavior of the cancer into the future. One big field is molecular markers of different types; they are tissue, urine, or blood-based markers.




View Conference Coverage
Online CME Activities
TitleExpiration DateCME Credits
Clinical Vignette Series: 34th Annual Chemotherapy Foundation Symposium: Innovative Cancer Therapy for Tomorrow®Feb 28, 20182.0
Community Practice Connections™: Personalized Sequencing in Castration-Resistant Prostate Cancer: Bridging the Latest Evidence to the Bedside in Clinical ManagementAug 25, 20181.5
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