Five-year outcomes of SABR in intermediate- and high-risk prostate cancer without ADT.

N Nidal Salim (European Medical Center, Moscow, Russian Federation) K Kristina Tumanova (European Medical Center, Moscow, Russian Federation) D Daria Zvereva (European Medical Center, Moscow, Russian Federation) A Alexey Popodko (European Medical Center, Moscow, Russian Federation) P Pavel Koposov (European Medical Center, Moscow, Russian Federation) N Nikolay Grigoriev (European Medical Center, Moscow, Russian Federation) E Eugene Libson (Hadassah Medical Center, Jerusalem, Israel)

Abstract

5101 Background: Stereotactic ablative body radiotherapy (SABR) is emerging as a prominent treatment option for localized prostate cancer (PCa). Most existing studies have primarily focused on low- and intermediate-risk PCa patients, who typically have favorable prognoses regardless of treatment. Additionally, the necessity of adding androgen deprivation therapy (ADT) remains a subject of ongoing debate, given its associated side effects and limited impact on overall survival (OS). In this study, we present the long-term outcomes of patients predominantly with intermediate- and high-risk PCa who were treated with SABR without ADT. Methods: This was a single-center prospective study of 87 patients with localized PCa who underwent SABR without subsequent ADT. SABR was delivered in an ultra-hypofractionation regimen (36.0 – 42.7 Gy) using Varian TrueBeam/EDGE linear accelerators between July 2015 and June 2024. The primary endpoint was biochemical recurrence-free survival (bRFS), with secondary endpoints including toxicity and overall survival (OS). Results: A total of 87 patients, with a median age of 68.8 years (range: 50–86 years), were included. The median follow-up period was 31 months (range: 3–105 months). The distribution of patients by risk group was as follows: low-risk (21.8%), intermediate-risk (55.1%), and high-risk (17.9%). The 1-, 3-, and 5-year bRFS rates were 97.6%, 92.2%, and 90.0%, respectively. Importantly, no patient died as a result of PCa progression during the observation period. No clinically significant toxicity was reported. Conclusions: The findings of this study suggest that SABR as a standalone treatment modality is a safe and effective approach for localized PCa, providing durable biochemical control without significant toxicity. However, further investigations involving larger patient cohorts and longer follow-up periods are needed to confirm these results and enhance their reliability.

Article Details

Volume / Issue Vol. 43, Issue 16_suppl
Published June 01, 2025
Pages 5101-5101
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (7)

N

Nidal Salim

European Medical Center, Moscow, Russian Federation

K

Kristina Tumanova

European Medical Center, Moscow, Russian Federation

D

Daria Zvereva

European Medical Center, Moscow, Russian Federation

A

Alexey Popodko

European Medical Center, Moscow, Russian Federation

P

Pavel Koposov

European Medical Center, Moscow, Russian Federation

N

Nikolay Grigoriev

European Medical Center, Moscow, Russian Federation

E

Eugene Libson

Hadassah Medical Center, Jerusalem, Israel