Update on Prostatectomy Versus Observation Trials

by Gerald L. Andriole, Jr., MD | Jul 2018

Gerald L. Andriole Jr., MD, presented “Update on Prostatectomy Versus Observation Trials” during the 23rd Annual Southwest Prostate Cancer Update on April 15, 2018 in Scottsdale, Arizona


How to cite: Andriole, Gerald L. “Update on Prostatectomy Versus Observation Trials” April 15, 2018. Accessed [date today]. https://dev.grandroundsinurology.com/Update-on-Prostatectomy-Versus-Observation-Trials/

Update on Prostatectomy Versus Observation TrialsSummary:

Gerald L. Andriole Jr., MD, who served on the cause of death ascertainment committee for the Prostate Intervention Versus Observation Trials (PIVOT), discusses PIVOT and criticisms to the trial design. He then analyzes similar trials testing definitive versus non-definitive treatment in low-risk disease.

PIVOT Objective and Results

In 2012, The New England Journal of Medicine published the randomized trial PIVOT. It tested whether or not the intent to treat with radical prostatectomy (RP) in men with screen-detected, clinically localized prostate cancer reduces mortality compared to observation. They published a follow-up article in 2017. Notably, the inclusion criteria required patients to have a PSA value of less than 50 ng per milliliter. Also, patients had to have had a predicted life expectancy of 10 years or longer.

Results showed that surgery did not reduce mortality in men with low PSA or low-risk prostate cancer. This observation, in conjunction with other trials, has increased urologists’ and patients’ awareness and acceptance of surveillance. On the other hand, PIVOT results support that surgery is likely beneficial for men with higher PSA and/or intermediate risk disease.  

Criticisms of PIVOT

However, the PIVOT trial had many limitations. Patient volunteers most likely had a higher severity of disease than in most RP series. Sextant biopsy determined the diagnoses for most of the patients in this trial, so some men considered to have low-risk disease likely harbored undiagnosed Gleason 4 pattern elements.

Furthermore, the trial design required 2000 patients, but only included 731 patients. Therefore, this trial was too underpowered to result in quality data. Issues with crossover and noncompliance may have diluted the trial results, as well.

Additional Prostatectomy versus Observation Studies

Additional randomized trials comparing definitive versus non-definitive treatment in early prostate cancer include The Scandinavian Prostate Cancer Group Study Number 4 (SPCG-4), the Prostate Testing for Cancer and Treatment (ProtecT) trial, and the Long-Term Follow-Up of a Large Active Surveillance Cohort of Patients With Prostate Cancer (led by Laurence Klotz, MD, FRCSC). The graphs below compare baseline characteristics and results of these three studies and PIVOT.

ABOUT THE AUTHOR

Gerald L. Andriole, Jr., MD, is the Robert K. Royce Distinguished Professor and Chief of Urologic Surgery at Barnes-Jewish Hospital, the Siteman Cancer Center, and Washington University School of Medicine in St. Louis, Missouri.

Dr. Andriole received his medical degree from Jefferson Medical College in Philadelphia, Pennsylvania. He trained in surgery at Strong Memorial Hospital and the University of Rochester and completed his Urology Residency at Brigham and Women’s Hospital and Harvard Medical School. Subsequently, he was a Fellow in Urologic Oncology at the National Cancer Institute in Bethesda, Maryland.

Dr. Andriole has over 35 years of consistent contributions in the areas of BPH and prostate cancer screening and prevention research. He has contributed well over 400 peer-reviewed publications and serves on the editorial boards of several prestigious journals. He is Chairman of the Prostate Committee of the National Cancer Institute’s Prostate, Lung, Colorectal and Ovarian (PLCO) Cancer Screening Trial, and PI of the NIDDK Multidisciplinary Approach to Urologic Pelvic Pain (MAPP) and Symptoms of Lower Urinary Tract Dysfunction Research Network (LURN). He was Chairman of the Steering Committee of the REDUCE Prostate Cancer Prevention Trial, as well as PI of both the NIDDK Medical Therapy of Prostatic Symptoms (MTOPS) BPH trial and the NIDDK Complementary and Alternative Medicine for Urinary Symptoms (CAMUS) study. He is a member of the American Urological Association, the American Association for Cancer Research, the American Society of Clinical Oncology, the American Surgical Association, the American Association of Genitourinary Surgeons, and the Clinical Society of Genitourinary Surgeons, among other societies.