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Ultrahypofractionated radiotherapy for localised prostate cancer: The impact of daily MRI-guided adaptive radiotherapy on delivered dose.

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Clinical and translational radiation oncology 📖 저널 OA 100% 2021: 2/2 OA 2022: 1/1 OA 2023: 1/1 OA 2024: 6/6 OA 2025: 17/17 OA 2026: 51/51 OA 2021~2026 2025 Vol.53() p. 100985
Retraction 확인
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PICO 자동 추출 (휴리스틱, conf 3/4)

유사 논문
P · Population 대상 환자/모집단
환자: localised prostate cancer, who received ultrahypofractionated MRIgART on the Unity MR linac (Elekta, Sweden) were retrospectively analysed
I · Intervention 중재 / 시술
ultrahypofractionated MRIgART on the Unity MR linac (Elekta, Sweden) were retrospectively analysed
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
[CONCLUSION] MRIgART, offers significant dosimetric benefit for ultrahypofractionated prostate cancer compared to non-adapted strategies. Greatest benefit is expected for those with SV or high-risk of SV involvement, persistent rectal gas, prostate swelling and for the application of novel dose strategies including GTV dose escalation and non-involved prostate dose de-escalation.

Alexander SE, Mitchell RA, Dunlop A, Herbert T, Morrison K, Nartey J, Oelfke U, McNair HA, Tree AC

📝 환자 설명용 한 줄

[INTRODUCTION] Magnetic resonance image-guided adaptive radiotherapy (MRIgART) reduces uncertainties by correcting for day-to-day target and organ-at-risk deformation and motion.

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↓ .bib ↓ .ris
APA Alexander SE, Mitchell RA, et al. (2025). Ultrahypofractionated radiotherapy for localised prostate cancer: The impact of daily MRI-guided adaptive radiotherapy on delivered dose.. Clinical and translational radiation oncology, 53, 100985. https://doi.org/10.1016/j.ctro.2025.100985
MLA Alexander SE, et al.. "Ultrahypofractionated radiotherapy for localised prostate cancer: The impact of daily MRI-guided adaptive radiotherapy on delivered dose.." Clinical and translational radiation oncology, vol. 53, 2025, pp. 100985.
PMID 40534639 ↗

Abstract

[INTRODUCTION] Magnetic resonance image-guided adaptive radiotherapy (MRIgART) reduces uncertainties by correcting for day-to-day target and organ-at-risk deformation and motion. This is the first study to examine the dosimetric impact of MRIgART for ultrahypofractionated prostate cancer treatment, compared to standard-of-care image-guided non-adapted radiotherapy.

[METHODS] Twenty patients with localised prostate cancer, who received ultrahypofractionated MRIgART on the Unity MR linac (Elekta, Sweden) were retrospectively analysed. Online daily MRI was acquired for replanning (MRI) and a second for position verification before treatment (MRI). To compare delivered dose with and without adaptation, three plans were generated offline per fraction; a session plan (reference plan adapted to MRI anatomy), a verification plan (session plan recalculated on MRI anatomy), and a non-adapted plan (reference plan recalculated on MRI anatomy). Target and organ-at-risk doses were calculated, and dose difference evaluated.Secondary analysis, using deformable dose accumulation, estimated verification and non-adapted dose to primary target (CTVpsv) substructures; prostate, gross tumour volume (GTV) and proximal 1 cm of seminal vesicles (1cmSV). Impact of prostate, rectum and bladder volume changes on dose were evaluated.

[RESULTS] Median dose to 95 % of the CTVpsv was significantly higher with adaptation; 40.3, 40.0 and 38.2 Gy for session, verification, and non-adapted plans. Adaptation achieved a lower median urethra V42Gy dose but bladder V37Gy dose was lower when not adapting. Rectum V36Gy dose was similar for adapted and non-adapted plans.CTVpsv substructure dose difference was greatest for 1cmSV; 40.0 versus 37.5 Gy for verification/non-adapted plans. Adaptation achieved significantly higher prostate only, but not GTV doses. Prostate and rectal volume changes had a negative impact on non-adapted dose only.

[CONCLUSION] MRIgART, offers significant dosimetric benefit for ultrahypofractionated prostate cancer compared to non-adapted strategies. Greatest benefit is expected for those with SV or high-risk of SV involvement, persistent rectal gas, prostate swelling and for the application of novel dose strategies including GTV dose escalation and non-involved prostate dose de-escalation.

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