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Feasibility of MR-guided ultrahypofractionated radiotherapy in 5, 2 or 1 fractions for prostate cancer.

Authors :
Mohajer J
Dunlop A
Mitchell A
Goodwin E
Nill S
Oelfke U
Tree A
Source :
Clinical and translational radiation oncology [Clin Transl Radiat Oncol] 2020 Oct 27; Vol. 26, pp. 1-7. Date of Electronic Publication: 2020 Oct 27 (Print Publication: 2021).
Publication Year :
2020

Abstract

The drive towards hypofractionated prostate radiotherapy is motivated by a low alpha/beta ratio for prostate cancer (1 to 3 Gy) compared to surrounding organs at risk, implying an improved therapeutic ratio with increasing dose per fraction. Early evidence from studies of ultrahypofractionated (UHF) prostate HDR brachytherapy has shown good tolerability in terms of normal tissue toxicities and clinical outcomes similar to conventional fractionation schedules. MR-guided stereotactic body radiotherapy (SBRT) with online plan adaptation and real-time tumour imaging may enable UHF doses to be delivered to the prostate safely, without the invasiveness of brachytherapy. The feasibility of UHF prostate treatment planning for the Unity MR-Linac (MRL, Elekta AB, Stockholm) was investigated for target prescriptions and planning constraints derived from the HDR brachytherapy and SBRT literature. Monaco 5.40 (Elekta) was used to generate MRL step-and-shoot IMRT plans for three dose fractionation protocols (5, 2 and 1 fractions), for ten randomly selected previously treated prostate cancer patients. Of the ten plans per UHF scheme, all clinical goals were met in all cases for 5 fractions, and in six cases for both 2 and 1 fraction schemes. PTV D95% was compromised by up to 6.4% and 3.9% of the associated target dose for 2 and 1 fraction plans respectively. There were two cases of PTV D95% compromise greater than a 5% dose decrease for the 2 fraction plans. The study suggests feasibility of the UHF treatment planning approaches if combined with real-time motion mitigation strategies.<br /> (© 2020 The Authors.)

Details

Language :
English
ISSN :
2405-6308
Volume :
26
Database :
MEDLINE
Journal :
Clinical and translational radiation oncology
Publication Type :
Academic Journal
Accession number :
33241129
Full Text :
https://doi.org/10.1016/j.ctro.2020.10.005