The Veterans Affairs Cooperative Studies Program study #553 was designed to evaluate the efficacy of adjuvant chemotherapy added to the standard of care (SOC) for patients who are at high risk for relapse after prostatectomy.
To test whether addition of chemotherapy to surgery for high-risk prostate cancer improves progression-free survival (PFS).
Eligible patients after prostatectomy were randomized to the SOC group with observation or to the chemotherapy group with docetaxel and prednisone administered every 3 wk for six cycles. Randomization was stratified for prostate-specific antigen, Gleason, tumor stage, and surgical margin status.
The primary endpoint was PFS. Secondary endpoints included overall, prostate cancer-specific, and metastasis-free survival, and time to androgen deprivation therapy.
A total of 298 of the planned 636 patients were randomized. The median follow-up was 59.1 mo (0.2-103.7 mo). For the primary endpoint, the two groups did not statistically differ in PFS (median 55.5 mo in the chemotherapy group and 42.2 mo in the SOC group; test adjusted for site via gamma frailty p=0.21; adjusted hazard ratio [HR] 0.80; 95% confidence interval [CI] 0.58-1.11; p=0.18). Prespecified subgroup analyses showed benefit in PFS for patients with tumor stage ≥T3b (HR 0.54, 95% CI 0.32-0.92; p=0.022) and patients with Gleason score ≤7 (HR 0.65, 95% CI 0.43-0.99; p=0.046). Secondary endpoint analyses are hampered by low event rates. The most common adverse events (≥grade 3 related or possibly related to chemotherapy) included neutropenia (43%), hyperglycemia (20%), and fatigue (5%), with febrile neutropenia in 2%.
Adjuvant chemotherapy in high-risk prostate cancer using docetaxel and prednisone did not lead to statistically significant improvement in PFS for the intention-to-treat population as a whole. The analysis was challenged by lower power due to accrual limitation. Subgroup analyses suggest potential benefit for patients with Gleason grade ≤7 and stage≥pT3b (ClinicalTrials.gov number NCT00132301).
In this randomized trial, we tested whether addition of chemotherapy to surgery for high-risk prostate cancer decreased the risk of prostate-specific antigen rise after surgery. We found no benefit from docetaxel given after radical prostatectomy, although some subgroups of patients may benefit.
European urology. 2020 Jan 07 [Epub ahead of print]
Daniel W Lin, Mei-Chiung Shih, William Aronson, Joseph Basler, Tomasz M Beer, Mary Brophy, Matthew Cooperberg, Mark Garzotto, W Kevin Kelly, Kelvin Lee, Valerie McGuire, Yajie Wang, Ying Lu, Vivian Markle, Unyime Nseyo, Robert Ringer, Stephen J Savage, Patricia Sinnott, Edward Uchio, Claire C Yang, R Bruce Montgomery
VA Puget Sound Health Care System, Seattle, WA, USA. Electronic address: ., VA Cooperative Studies Program, Albuquerque, NM, USA., West LA VA, Los Angeles, CA, USA., San Antonio VA, San Antonio, TX, USA., Portland VA, Portland, OR, USA., San Francisco VA, San Francisco, CA, USA., West Haven VA, West Haven, CT, USA., Stanford University, Stanford, CA, USA., VA Puget Sound Health Care System, Seattle, WA, USA., Gainesville VA, Gainesville, VA, USA., Charleston VA, Charleston, SC, USA.