본문으로 건너뛰기
← 뒤로

Primary Endpoint Analysis of the Phase 2 DESTINATION-MRL Trial for Patients With Intermediate-Risk Prostate Cancer.

International journal of radiation oncology, biology, physics 2026 Vol.125(1) p. 257-265 🌐 cited 1 🔓 OA Prostate Cancer Diagnosis and Treatm
TL;DR While toxicity-minimizing radiotherapy in online adaptive MRI-guided SBRT for PCa was feasible in 2 of the 3 institutes, robust coverage of the GTV and CTV could not be assured in the absence of a gating strategy.
OpenAlex 토픽 · Prostate Cancer Diagnosis and Treatment Advanced Radiotherapy Techniques Prostate Cancer Treatment and Research

Dassen MG, Tree AC, Wiersema L, Neijndorff B, de Ruiter P, van der Linden J, Mitchell A, Dunlop A, Alexander S, Breitkreutz DY, Cooper S, Janssen T, Pos F, Vesprini D, van der Heide UA

📝 환자 설명용 한 줄

While toxicity-minimizing radiotherapy in online adaptive MRI-guided SBRT for PCa was feasible in 2 of the 3 institutes, robust coverage of the GTV and CTV could not be assured in the absence of a gat

이 논문을 인용하기

BibTeX ↓ RIS ↓
APA Mathijs G. Dassen, Alison Tree, et al. (2026). Primary Endpoint Analysis of the Phase 2 DESTINATION-MRL Trial for Patients With Intermediate-Risk Prostate Cancer.. International journal of radiation oncology, biology, physics, 125(1), 257-265. https://doi.org/10.1016/j.ijrobp.2025.11.028
MLA Mathijs G. Dassen, et al.. "Primary Endpoint Analysis of the Phase 2 DESTINATION-MRL Trial for Patients With Intermediate-Risk Prostate Cancer.." International journal of radiation oncology, biology, physics, vol. 125, no. 1, 2026, pp. 257-265.
PMID 41314554

Abstract

[PURPOSE] Escalating dose to the gross tumor volume (GTV) while de-escalating dose to the prostate clinical target volume (CTV) and using a 0-mm planning target volume margin can potentially minimize toxicity without compromising biochemical control in patients with intermediate-risk prostate cancer. We evaluated the technical feasibility of this approach in online adaptive magnetic resonance imaging (MRI)-guided stereotactic body radiation therapy.

[METHODS AND MATERIALS] The DESTINATION-MRL trial ran as 3 parallel single-center phase 2 non-randomized trials in 3 different institutes. Each institute enrolled 20 patients who were all treated on a 1.5T Unity MR-linear accelerator (MR-Linac). The GTV was defined as tumor(s) visible on multiparametric MRI. The CTV was defined as the whole prostate. The proximal 1-2 cm of the seminal vesicles were included in the CTV at the clinician's discretion. An intraprostatic margin of 4 mm was applied to the GTV to account for delineation and pathological uncertainty (GTV 4 mm) and no planning target volume margin was applied to the CTV. All patients were treated with 30 Gy in 5 fractions to the CTV and an isotoxic boost of 45 Gy to the GTV 4 mm. The primary endpoint was technical feasibility, defined as an accumulated GTV D90% of >42 Gy on the post-treatment MRI in ≥90% of the patients.

[RESULTS] Between May 2023 and September 2024, 60 patients were treated, of which 54 were included for analysis. An accumulated GTV D90% of >42 Gy was reached in 46 patients (85%). Analysis per institute showed that this criterion was reached in 10 of 14 patients (71%) in institute 1 and in 18 of 20 patients (90%) in both institutes 2 and 3.

[CONCLUSIONS] Although toxicity-minimizing radiation therapy in online adaptive MRI-guided stereotactic body radiation therapy for prostate cancer was feasible in 2 of the 3 institutes, robust coverage of the GTV and CTV could not be assured in the absence of a gating strategy.

MeSH Terms

Humans; Male; Prostatic Neoplasms; Radiosurgery; Aged; Radiotherapy, Image-Guided; Magnetic Resonance Imaging; Feasibility Studies; Middle Aged; Tumor Burden; Radiotherapy Planning, Computer-Assisted; Radiotherapy Dosage; Aged, 80 and over; Organs at Risk; Endpoint Determination

같은 제1저자의 인용 많은 논문 (1)