Adjuvant and salvage radiotherapy after neoadjuvant therapy and radical prostatectomy for high‐risk localized prostate cancer

Author:

Ravi Praful1ORCID,Kwak Lucia1,Devlies Wout2,Xie Wanling1,Chipidza Fallon3,Yang Xiaoyu1,Bubley Glenn4,Kaplan Irving4,Kibel Adam S.5ORCID,Nguyen Paul3,Taplin Mary‐Ellen1

Affiliation:

1. Lank Center for Genitourinary Oncology Dana‐Farber Cancer Institute Boston Massachusetts USA

2. Department of Urology KU Leuven Leuven Belgium

3. Department of Radiation Oncology Brigham & Women's Hospital Boston Massachusetts USA

4. Beth Israel Deaconess Medical Center Boston Massachusetts USA

5. Department of Urology Brigham & Women's Hospital Boston Massachusetts USA

Abstract

AbstractBackgroundWe sought to describe patterns of delivery of adjuvant (aRT) and salvage RT (sRT) in patients who underwent RP after receiving neoadjuvant androgen receptor pathway inhibitor (ARPI) before radical prostatectomy (RP) for high‐risk localized prostate cancer (HRLPC).MethodsTwo hundred eighteen patients treated on phase 2 neoadjuvant trials between 2006 and 2018 at two academic centers were evaluated. aRT and sRT were defined as receipt of RT with a PSA of ≤0.1 or >0.1 ng/mL, respectively. Primary outcomes were biochemical recurrence (BCR), defined as time from aRT/sRT to a PSA rising to >0.1 ng/mL, and metastasis‐free survival (MFS) after RT.ResultsTwenty‐three (11%) and 55 (25%) patients received aRT and sRT respectively. Median PSA at start of aRT and sRT was 0.01 and 0.16 ng/mL, and median duration from RP to RT was 5 and 14 months, respectively. All aRT patients had NCCN high‐risk disease, 30% were pN1 and 43% had positive surgical margins; 52% had prostate bed RT. Fifty‐one percent of sRT patients had biopsy Gleason 9–10, 29% were pT2 and 9% had positive surgical margins; 63% had RT to the prostate bed/pelvis. At a median follow‐up of 5.3 and 3.0 years after aRT and sRT, 3‐year freedom from BCR was 55% and 47%, and 3‐year MFS was 56% and 53%, respectively.ConclusionsaRT was infrequently used in patients who received neoadjuvant ARPI before RP for HRLPC. Outcomes of aRT and sRT were similar but generally poor. Studies evaluating intensified systemic therapy approaches with postoperative RT in this high‐risk population are needed.

Publisher

Wiley

Subject

Urology,Oncology

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