ESTRO 2024 - Abstract Book

S2475

Clinical - Urology

ESTRO 2024

5.Arrayeh E, Westphalen AC, Kurhanewicz J, Roach M, 3rd, Jung AJ, Carroll PR, et al. Does local recurrence of prostate cancer after radiation therapy occur at the site of primary tumor? Results of a longitudinal MRI and MRSI study. Int J Radiat Oncol Biol Phys. 2012;82(5):e787-93.

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Prostate Cancer ultra-hypofractionation: single-center late tolerance analysis, two-years data

Ilaria Bonavero 1 , Giuseppe Carlo Iorio 1 , Sara Bartoncini 1 , Elena Gallio 2 , Diego Bongiovanni 1 , Sara Gaspari 1 , Valeria Chiofalo 3 , Cristiano Grossi 1 , Fabio Menegatti 1 , Edoardo Gozzelino 1 , Erica Cuffini 3 , Giuliana Petruzzelli 1 , Marzia Cerrato 1 , Bruna Lo Zito 1 , Chiara Casale 1 , Francesca Catena 1 , Eulalie Joelle Tondji Ngassam 1 , Mario Levis 1 , Parise Ramona 1 , Umberto Ricardi 1 1 University of Turin, Department of Oncology, Turin, Italy. 2 University of Turin, Department of Medical Physics, Turin, Italy. 3 University of Turin, Department of Oncology, Turin, Japan

Purpose/Objective:

Late tolerance evaluation of ultra-hypofractionated RT for localised (low- to high-risk) prostate cancer (PCa).

Material/Methods:

This late toxicity analysis pertains to a single-center cohort of patients (pts) treated with LINAC-based VMAT ultra hypofractionation (42.7 Gy/7 fractions every other day; 15-19 days). The treatment was delivered with daily IGRT (Cone-Beam CT). No fiducials nor spacers were employed. The CTV – PTV margin was 7 mm (5 mm towards the rectum). The CTV was defined as the prostate only for low-risk (LR) pts. CTV included proximal seminal vesicles (SVs) in intermediate-risk PCa and distal SVs for high-risk pts (HR). Whole SVs were included in the case of cT3b. Hormonal therapy prescription (HT) was at the physician's discretion in unfavorable-intermediate PCa (UIR) and mandatory in HR. Genitourinary (GU) and gastrointestinal (GI) toxicity were scored according to RTOG. The IPSS (≤12 or >12) was also assessed. Timepoints of the late toxicity report were: 6-, 12-, 18-, and 24-months from the RT end. Additionally, a statistical analysis (logistic regression analysis) was performed to identify the predictive risk factors of late (6- to 24- months from the RT end) GU G2+ events. Among the investigated factors: risk-group, previous TURP, baseline alpha- blocker administration, baseline IPSS value, prostate volume (≤ or > 80cc), HT administration, overall treatment time (OTT, ≤17 or >17 days), bladder V37 Gy (≤10cc, ≤15cc, ≤20cc, >20cc), GU acute toxicity.

Results:

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