Postradical prostatectomy prostate‐specific antigen outcomes after 6 versus 18 months of perioperative androgen‐deprivation therapy in men with localized, unfavorable intermediate–risk or high‐risk prostate cancer: Results of part 2 of a randomized phase 2 trial

Author:

McKay Rana R.12ORCID,Xie Wanling3,Yang Xiaoyu4,Acosta Andres5,Rathkopf Dana6,Laudone Vincent P.7,Bubley Glenn J.3,Einstein David J.8,Chang Peter9,Wagner Andrew A.9,Kane Christopher J.2,Preston Mark A.10,Kilbridge Kerry4,Chang Steven L.10,Choudhury Atish D.4,Pomerantz Mark M.4ORCID,Trinh Quoc‐Dien10,Kibel Adam S.10,Taplin Mary‐Ellen4

Affiliation:

1. Department of Medicine University of California San Diego La Jolla California USA

2. Department of Urology University of California San Diego La Jolla California USA

3. Department of Data Science Dana‐Farber Cancer Institute Boston Massachusetts USA

4. Department of Medical Oncology Dana‐Farber Cancer Institute Boston Massachusetts USA

5. Department of Pathology Brigham and Women’s Hospital Boston Massachusetts USA

6. Department of Medicine Memorial Sloan Kettering Cancer Center New York New York USA

7. Department of Surgery Memorial Sloan Kettering Cancer Center New York New York USA

8. Department of Medicine Beth Israel Deaconess Medical Center Boston Massachusetts USA

9. Department of Surgery Beth Israel Deaconess Medical Center Boston Massachusetts USA

10. Department of Surgery Brigham and Women’s Hospital Boston Massachusetts USA

Abstract

AbstractBackgroundPatients with localized, unfavorable intermediate–risk and high‐risk prostate cancer have an increased risk of relapse after radical prostatectomy (RP). The authors previously reported on part 1 of this phase 2 trial testing neoadjuvant apalutamide, abiraterone, prednisone, plus leuprolide (AAPL) or abiraterone, prednisone, and leuprolide (APL) for 6 months followed by RP. The results demonstrated favorable pathologic responses (tumor <5 mm) in 20.3% of patients (n = 24 of 118). Herein, the authors report the results of part 2.MethodsFor part 2, patients were randomized 1:1 to receive either AAPL for 12 months (arm 2A) or observation (arm 2B), stratified by neoadjuvant therapy and pathologic tumor classification. The primary end point was 3‐year biochemical progression‐free survival. Secondary end points included safety and testosterone recovery (>200 ng/dL).ResultsOverall, 82 of 118 patients (69%) enrolled in part 1 were randomized to part 2. A higher proportion of patients who were not randomized to adjuvant therapy had a favorable prostatectomy pathologic response (32.3% in nonrandomized patients compared with 17.1% in randomized patients). In the intent‐to‐treat analysis, the 3‐year biochemical progression‐free survival rate was 81% for arm 2A and 72% for arm 2B (hazard ratio, 0.81; 90% confidence interval, 0.43–1.49). Of the randomized patients, 81% had testosterone recovery in the AAPL group compared with 95% in the observation group, with a median time to recovery of <12 months in both arms.ConclusionsIn this study, because 30% of patients declined adjuvant treatment, part B was underpowered to detect differences between arms. Future perioperative studies should be biomarker‐directed and include strategies for investigator and patient engagement to ensure compliance with protocol procedures.

Publisher

Wiley

Subject

Cancer Research,Oncology

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