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Fractionated stereotactic body radiotherapy for up to five prostate cancer oligometastases: Interim outcomes of a prospective clinical trial
Authors:Patrick Bowden  Andrew W. See  Mark Frydenberg  Hodo Haxhimolla  Anthony J. Costello  Daniel Moon  Paul Ruljancich  Jeremy Grummet  Alan Crosthwaite  Ganes Pranavan  Justin S. Peters  Kevin So  Stella M. Gwini  Dean P. McKenzie  Skye Nolan  Lloyd M.L. Smyth  Craig Everitt
Affiliation:1. Icon Cancer Centre, Richmond, VIC, Australia;2. Department of Surgery, Monash University, Clayton, VIC, Australia

Australian Urology Associates, Melbourne, VIC, Australia;3. Department of Urology, The Canberra Hospital, Canberra, ACT, Australia

Australian National University, Canberra, ACT, Australia;4. Department of Surgery, University of Melbourne, Parkville, VIC, Australia;5. Department of Surgery, University of Melbourne, Parkville, VIC, Australia

Division of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia

Epworth HealthCare, Richmond, VIC, Australia;6. Epworth Eastern, Box Hill, VIC, Australia;7. Department of Surgery, Monash University, Clayton, VIC, Australia

Epworth HealthCare, Richmond, VIC, Australia;8. Department of Medical Oncology, The Canberra Hospital, Canberra, ACT, Australia;9. Department of Surgery, University of Melbourne, Parkville, VIC, Australia

Epworth HealthCare, Richmond, VIC, Australia

Department of Urology, Royal Melbourne Hospital, Parkville, VIC, Australia;10. School of Public Health and Preventive Medicine, Monash University, Clayton, VIC, Australia;11. Epworth HealthCare, Richmond, VIC, Australia

School of Public Health and Preventive Medicine, Monash University, Clayton, VIC, Australia

Abstract:Stereotactic body radiotherapy (SBRT) can delay escalation to systemic treatment in men with oligometastatic prostate cancer (PCa). However, large, prospective studies are still required to evaluate the efficacy of this approach in different patient groups. This is the interim analysis of a prospective, single institution study of men relapsing with up to five synchronous lesions following definitive local treatment for primary PCa. Our aim was to determine the proportion of patients not requiring treatment escalation following SBRT. In total, 199 patients were enrolled to receive fractionated SBRT (50 Gray in 10 fractions) to each visible lesion. Fourteen patients were castration resistant at enrolment. The proportion of patients not requiring treatment escalation 2 years following SBRT was 51.7% (95% CI: 44.1–59.3%). The median length of treatment escalation-free survival over the entire follow-up period was 27.1 months (95% CI; 21.8–29.4 months). Prior androgen deprivation therapy (ADT) predicted a significantly lower rate of freedom from treatment escalation at 2 years compared to no prior ADT (odds ratio = 0.21, 95% CI: 0.08–0.54, p = 0.001). There was no difference in the efficacy of SBRT when treating 4–5 vs. 1–3 initial lesions. A prostate-specific antigen (PSA) decline was induced in 75% of patients, with PSA readings falling to an undetectable level in six patients. No late grade three toxicities were observed. These interim results suggest that SBRT can be used to treat up to five synchronous PCa oligometastases to delay treatment escalation.
Keywords:androgen deprivation therapy  oligometastases  prostate cancer  stereotactic body radiotherapy
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