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Expert Sheds Light on Prostate Cancer Screening Trial

Danielle Bucco
Published: Wednesday, Nov 08, 2017

E. David Crawford, MD
E. David Crawford, MD
The European Randomized Study of Screening for Prostate Cancer (ERSPC) and United States Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial (PLCO) showed varying results in mortality when investigating screening for men with prostate cancer.

These randomized, controlled trials evaluated the effects of screening versus no screening on mortality. ERSPC found that screening reduced prostate cancer mortality, whereas the PLCO trial found no reduction.

However, a recent analysis published in the Annals of Internal Medicine concluded through statistical models accounting for differences in implementation and settings that ERSPC and PLCO offer compatible evidence that screening lowers prostate cancer mortality.

In an interview with OncLive, E. David Crawford, MD, a professor of radiation oncology at the University of Colorado, discusses the controversy surrounding the PLCO trial, as well as the role of prostate-specific antigen (PSA) testing for men with prostate cancer.

OncLive: Can you please provide some background of the PLCO study?

Crawford: We initiated the 2 big screening trials with Europe and the United States. There were 10 centers involved in the United States screening trial. It started out looking at screening for prostate cancer but got held up by the National Institutes of Health because there was an interest in adding other cancers to this screening trial. It took 3 years from the time we planned on starting this in prostate cancer for it to be launched as a PLCO trial in prostate, lung, colorectal, and ovarian cancer.  

Unfortunately, in the interim, men were getting screened with the PSA test in the United States. The population of unscreened men did not exist like it did a few years prior. Also, during the trial, when people were randomized to the usual care, which did not involve screening, they would go out and get screened. The contamination became an issue in the United States trial. We recognized that and accounted for it in the statistical analysis—accepting a 25% to 30% contamination.  

The contamination got worse, so the control arm contamination was around 50% to 90% over time. It looked at the binary statistics of doing a study like this. It was screen versus no screening, but since there were contaminations in the no-screen arm, many felt that this trial lost its power. What this study did was look at it in a different way.  

The European trial was not faced with that dilemma of screening since it was not accepted at that time. They had a population that was more urgent and did not enter screening off the protocol. They essentially had a purer no-screening arm. When these studies were originally reported at 8 years, there was no difference. However, with 10 to 15 years, the European trial showed a difference of 25% to 30% improvement in mortality.

Our trial was sort of trashed in a way by many people because of the contamination. It’s a negative trial and did not seem to be a benefit for people. Many write it off as a waste of money, time, and effort, which is both true and not true.   Myself and Dr Anthony D’Amico tried to salvage this study 7 to 8 years ago. We looked at the PLCO trial and the performance status for patients who entered the trial quite healthy and we saw a benefit.

A group got together—including myself and some of the others who were on the original trial— to look at a promising new way to analyze the data. We investigated the intensity of screening, not just an occasional PSA as an endpoint. We tried to look at the PLCO trial and reconcile it to the point where it was compared with the European trial—showing that there is more of a benefit than baseline intensity. It is important to do longer follow-up to see a benefit for prostate cancer screening. Now, there is a benefit of 10, 15, and 20 years and a 25% to 30% improvement in survival rates.

Some screening is good. We see it with the mortality rates when we look at the number of metastatic disease [cases] that occurred back in 1989 when we started screening. The incidence of metastatic disease dropped precipitously; whereas, in breast cancer over the years, there wasn’t any change in metastatic disease. In prostate cancer, we saw the drop in metastatic disease and, therefore, over enough time, we saw an improvement in survival rate. Data in the US Preventive Services Task Force (USPSTF) are focusing on the downside, which was right. There was overdiagnosis and overtreatment. However, right now, these data couldn’t come at a better time for prostate cancer.


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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