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Clinical Trial
. 2020 May 1;6(5):650-659.
doi: 10.1001/jamaoncol.2020.0147.

Outcomes of Observation vs Stereotactic Ablative Radiation for Oligometastatic Prostate Cancer: The ORIOLE Phase 2 Randomized Clinical Trial

Ryan Phillips  1 , William Yue Shi  2 , Matthew Deek  1 , Noura Radwan  1 , Su Jin Lim  3 , Emmanuel S Antonarakis  3 , Steven P Rowe  4   5 , Ashley E Ross  5 , Michael A Gorin  4   5 , Curtiland Deville  1 , Stephen C Greco  1 , Hailun Wang  1 , Samuel R Denmeade  3 , Channing J Paller  3 , Shirl Dipasquale  1 , Theodore L DeWeese  1   3   5 , Daniel Y Song  1   3   5 , Hao Wang  3 , Michael A Carducci  3 , Kenneth J Pienta  3   5 , Martin G Pomper  4   5 , Adam P Dicker  6 , Mario A Eisenberger  3 , Ash A Alizadeh  7 , Maximilian Diehn  2 , Phuoc T Tran  1   3   5
Affiliations
Clinical Trial

Outcomes of Observation vs Stereotactic Ablative Radiation for Oligometastatic Prostate Cancer: The ORIOLE Phase 2 Randomized Clinical Trial

Ryan Phillips et al. JAMA Oncol. .

Abstract

Importance: Complete metastatic ablation of oligometastatic prostate cancer may provide an alternative to early initiation of androgen deprivation therapy (ADT).

Objective: To determine if stereotactic ablative radiotherapy (SABR) improves oncologic outcomes in men with oligometastatic prostate cancer.

Design, setting, and participants: The Observation vs Stereotactic Ablative Radiation for Oligometastatic Prostate Cancer (ORIOLE) phase 2 randomized study accrued participants from 3 US radiation treatment facilities affiliated with a university hospital from May 2016 to March 2018 with a data cutoff date of May 20, 2019, for analysis. Of 80 men screened, 54 men with recurrent hormone-sensitive prostate cancer and 1 to 3 metastases detectable by conventional imaging who had not received ADT within 6 months of enrollment or 3 or more years total were randomized.

Interventions: Patients were randomized in a 2:1 ratio to receive SABR or observation.

Main outcomes and measures: The primary outcome was progression at 6 months by prostate-specific antigen level increase, progression detected by conventional imaging, symptomatic progression, ADT initiation for any reason, or death. Predefined secondary outcomes were toxic effects of SABR, local control at 6 months with SABR, progression-free survival, Brief Pain Inventory (Short Form)-measured quality of life, and concordance between conventional imaging and prostate-specific membrane antigen (PSMA)-targeted positron emission tomography in the identification of metastatic disease.

Results: In the 54 men randomized, the median (range) age was 68 (61-70) years for patients allocated to SABR and 68 (64-76) years for those allocated to observation. Progression at 6 months occurred in 7 of 36 patients (19%) receiving SABR and 11 of 18 patients (61%) undergoing observation (P = .005). Treatment with SABR improved median progression-free survival (not reached vs 5.8 months; hazard ratio, 0.30; 95% CI, 0.11-0.81; P = .002). Total consolidation of PSMA radiotracer-avid disease decreased the risk of new lesions at 6 months (16% vs 63%; P = .006). No toxic effects of grade 3 or greater were observed. T-cell receptor sequencing identified significant increased clonotypic expansion following SABR and correlation between baseline clonality and progression with SABR only (0.082085 vs 0.026051; P = .03).

Conclusions and relevance: Treatment with SABR for oligometastatic prostate cancer improved outcomes and was enhanced by total consolidation of disease identified by PSMA-targeted positron emission tomography. SABR induced a systemic immune response, and baseline immune phenotype and tumor mutation status may predict the benefit from SABR. These results underline the importance of prospective randomized investigation of the oligometastatic state with integrated imaging and biological correlates.

Trial registration: ClinicalTrials.gov Identifier: NCT02680587.

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Conflict of interest statement

Conflict of Interest Disclosures: Dr Phillips reported receiving consulting fees and honoraria from RefleXion Medical outside the submitted work. Mr Shi reported receiving support from the Alpha Omega Alpha Carolyn L. Kuckein Student Research Fellowship. Dr Antonarakis reported receiving research grants to his institution from Dendreon, Genentech, Novartis, Janssen, Johnson & Johnson, Sanofi, Bristol-Myers Squibb, Pfizer, AstraZeneca, Celgene, Merck & Co, Bayer, and Clovis; serving as a paid consultant/advisor to Astellas Pharma, Janssen, Pfizer, Sanofi, Dendreon, Bayer, Bristol-Myers Squibb, Amgen, Merck & Co, AstraZeneca, and Clovis outside the submitted work; and holding a patent to a biomarker technology licensed to Qiagen. Drs Rowe and Gorin reported receiving research funding and consulting fees from Progenics Pharmaceuticals, the licensee of 18F-DCFPyL, outside the submitted work. Dr Carducci reported receiving personal fees from Pfizer and Roche/Genentech for serving on data safety monitoring boards outside the submitted work. Dr Pienta reported receiving grants from Progenics Pharmaceuticals and the Prostate Cancer Foundation, consulting fees and stock options from Cue Biopharma, and consulting fees from GloriousMed Technology outside the submitted work. Dr Pomper reported receiving grants and other from Progenics Pharmaceuticals and grants from the National Institutes of Health during the conduct of the study, as well as holding a patent (US 8,778,305 B2) covering 18F-DCFPyL with royalties paid (Progenics Pharmaceuticals). Dr Dicker reported receiving grants from the Prostate Cancer Foundation, the National Cancer Institute, and NRG Oncology during the conduct of the study; receiving advisor fees from Janssen, Cybrexa Therapeutics, Self Care Catalysts, OncoHost, ThirdBridge, Noxopharm, Celldex Therapeutics, EMD Serono, and Roche; providing expert testimony on intellectual property for Wilson Sonsini; and serving as an unpaid advisor for Google LaunchPad Accelerator, Dreamit Ventures, and Evolution Road outside the submitted work. Dr Alizadeh reported receiving consulting fees from Roche, Genentech, Chugai Pharmaceutical Co, and Pharmacyclics outside the submitted work; having equity in Forty Seven and CiberMed; and being a coinventor on patent applications related to CAPP-Seq. Dr Diehn reported receiving grants and personal fees from Illumina; receiving consulting fees from Roche, AstraZeneca, BioNTech, Novartis, Varian Medical Systems, and Quanticel Pharmaceuticals; receiving honoraria from RefleXion Medical; and having equity in CiberMed outside the submitted work, as well as being a coinventor and having pending and issued patents related to CAPP-Seq. Dr Tran reported receiving grants from RefleXion Medical, the Prostate Cancer Foundation, and Movember Foundation during the conduct of the study; receiving grants from Astellas Pharma and Bayer and personal fees from Noxopharm and RefleXion Medical outside the submitted work; and holding a licensed patent related to ablative radiotherapy compounds and methods (Natsar Pharmaceuticals).

Figures

Figure 1.
Figure 1.. CONSORT Diagram
Figure 2.
Figure 2.. Clinical Outcomes of Stereotactic Ablative Radiotherapy (SABR) Compared With Observation and Benefit of Total Consolidation of Prostate-Specific Membrane Antigen Radiotracer-Avid Lesions
A, Composite progression-free survival (PFS) stratified by study arm. B, Biochemical PFS stratified by study arm. C, Composite PFS and (D) distant metastasis–free survival (DMFS) for patients treated by SABR stratified by presence of untreated lesions detected by prostate-specific membrane antigen–positron emission tomography.
Figure 3.
Figure 3.. Baseline and Dynamic Immunologic Features Suggesting Interplay Between Stereotactic Ablative Radiotherapy (SABR) and the Immune System
A, Changes in T-cell clonotype abundance at day 90 from baseline. B, Baseline Simpson clonality stratified by progression at 180 days. C, Clustered T-cell receptor sequences identified at day 90 in 3 patients treated with SABR.
Figure 4.
Figure 4.. Association of High-Risk Mutation Status With Progression-Free Survival (PFS) After Stereotactic Ablative Radiotherapy (SABR)
A, Patient characteristics and tumor mutations for patients with detectable circulating tumor DNA via CAPP-Seq or pathogenic germline mutations. B, PFS stratified by treatment arm for patients without high-risk mutations (n = 15). C, PFS stratified by treatment arm for patients with high-risk mutations (n = 7).
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