Stereotactic radiotherapy for localized prostate cancer: 10-year outcomes from three prospective trials

Menée auprès de 267 patients atteints d'un cancer de la prostate de stade localisé et inclus dans 3 essais cliniques canadiens entre 2006 et 2013 (durée médiane de suivi : 10,3 ans), cette étude analyse l'efficacité, du point de vue de la survie globale et du taux de récidive biochimique, d'une radiothérapie stéréotaxique d'ablation

International journal of radiation oncology, biology, physics, sous presse, 2024, article en libre accès

Résumé en anglais

Background and purpose: Stereotactic ablative radiotherapy (SABR) is growingly accepted for the treatment of localized prostate cancer with recent randomized trials showing non-inferiority compared to conventional or moderately hypofractionated radiotherapy. The natural history of prostate cancer necessitates extended surveillance for recurrence; however, there are few prospective studies reporting long-term outcomes.

Materials and methods: This study included patients with low and intermediate risk localized prostate cancer from three Canadian clinical trials enrolled from 2006-2013. All patients received SABR to the prostate consisting of 35-40 Gy in 5 fractions over 11-29 days. PSA, distant metastasis, and vital status were prospectively recorded. Occurrence of second malignancy after treatment was assessed by chart review and classified using modified Cahan's criteria.

Results: 267 patients were included. Median follow up was 10.3 years (IQR 7.8 – 12.7). 10-year BF (95% CI) was 7.7% (3.9-11.5). 10-year OS, PCSS, and FFM were 84.1% (79.3 – 89.1%), 99.2% (98.1 – 100), and 98.8% (97.5-100), respectively. 27/267 (10.1%) patients experienced a SM, with 6/27 patients (22.2%) classified as having a SM likely (n=3) or possibly (n=3) related to prior radiotherapy. 10-year freedom from SM was 89.2%.

Conclusion: SABR shows excellent long-term disease control for low and intermediate risk localized prostate cancer. Patients treated for prostate cancer have a moderate risk of second malignancy, consistent with background rates for the population.