4.6 Article

Curative-intent Metastasis-directed Therapies for Molecularly- defined Oligorecurrent Prostate Cancer: A Prospective Phase II Trial Testing the Oligometastasis Hypothesis

Journal

EUROPEAN UROLOGY
Volume 80, Issue 3, Pages 374-382

Publisher

ELSEVIER
DOI: 10.1016/j.eururo.2021.02.031

Keywords

Metastasis directed treatment; Oligometastasis; Prostate cancer; PSMA PET; SABR

Funding

  1. Terry Fox Canadian Comprehensive Cancer Centre Network (TF4CN) Pilot Project, Terry Fox Research Institute (TFRI)
  2. Abbvie CARO (Canadian Association of Radiation Oncology) Uro-Oncologic Radiation Awards (ACURA)
  3. Astellas Prostate Cancer Innovation Fund, University of Toronto
  4. Princess Margaret Cancer Foundation

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This study investigated the role of PSMA-targeted PET-MR/CT in the diagnosis and treatment of PCa patients, identifying the presence of oligorecurrent-PCa and its potential therapeutic effects in a subset of patients.
Background: The hypothesis of a curable oligometastatic prostate cancer (PCa) state remains to be clinically-proven. Conventional imaging often fails to localize early recurrences, hampering the potential for radical approaches. Objective: We hypothesize that prostate-specific membrane antigen (PSMA)-targeted PET-MR/CT allows for earlier detection and localization of oligorecurrent-PCa, unveiling a molecularly-defined state amenable to curative-intent metastasis-directed treatment (MDT). Design/setting/participants: Single-institution single-arm phase-two study. Patients with rising PSA (0.4-3.0 ng/mL) after maximal local therapy (radical prostatectomy and post-operative radiotherapy), negative conventional staging, and no prior salvage hormonal therapy (HT) were eligible. Interventions: All patients underwent [F-18]DCFPyL PET-MR/CT. Patients with molecularly-defined oligorecurrent-PCa had MDT (stereotactic ablative body radiotherapy [SABR] or surgery) without HT. Outcome measurements/statistical analysis: Primary endpoint was biochemical response (complete, i.e. biochemical 'no evidence of disease' [bNED], or partial response [100% or >= 50% PSA decline from baseline, respectively]) after MDT. Simon's two-stage design was employed (null and alternate hypotheses <5% and >20% response rate, respectively), with alpha and beta of 0.1. Results: Seventy-two patients were enrolled (May/2017-July/2019). Thirty-eight (53%) had PSMA-detected oligorecurrent-PCa amenable for MDT. Thirty-seven (51%) agreed to MDT: 10 and 27 underwent surgery and SABR, respectively. Median follow-up was 15.9 months (IQR 9.8-19.1). Of patients receiving MDT, the overall response rate was 60%, including 22% rendered bNED. One (2.7%) grade 3 toxicity (intra-operative ureteric injury) was observed. Conclusions: PSMA-defined oligorecurrent-PCa can be rendered bNED, a necessary step towards cure, in 1 of 5 patients receiving MDT alone. Randomized trials are justified to determine if MDT +/-systemic agents can expand the curative therapeutic armamentarium for PCa. Patient summary: We studied men treated for prostate cancer with rising PSA. We found PSMA imaging detected recurrent cancer in three-quarters of patients, and targeted treatment to these areas significantly decreased PSA in half of patients. (C) 2021 European Association of Urology. Published by Elsevier B.V. All rights reserved.

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