Background and purpose: Recently, intermediate and high-risk prostate cancer patients have been treated in a multicenter phase II trial with extremely hypofractionated prostate radiotherapy (hypo-FLAME trial). The purpose of the current study was to investigate whether a 1.5 T magnetic resonance imaging guided linear accelerator (MRI-linac) could achieve complex dose distributions of a quality similar to conventional linac stateof-the-art prostate treatments. Materials and methods: The clinically delivered treatment plans of 20 hypo-FLAME patients (volumetric modulated arc therapy, 10 MV, 5 mm leaf width) were included. Prescribed dose to the prostate was 5 × 7 Gy, with a focal tumor boost up to 5 × 10 Gy. MRI-linac treatment plans (intensity modulated radiotherapy, 7 MV, 7 mm leaf width, fixed collimator angle and 1.5 T magnetic field) were calculated. Dose distributions were compared. Results: In both conventional and MRI-linac treatment plans, the V35Gy to the whole prostate was > 99% in all patients. Mean dose to the gross tumor volume was 45 Gy for conventional and 44 Gy for MRI-linac plans, respectively. Organ at risk doses were met in the majority of plans, except for a rectal V35Gy constraint, which was exceeded in one patient, by 1 cc, for both modalities. The bladder V32Gy and V28Gy constraints were exceeded in two and one patient respectively, for both modalities. Conclusion: Planning of stereotactic radiotherapy with focal ablative boosting in prostate cancer on a high field MRI-linac is feasible with the current MRI-linac properties, without deterioration of plan quality compared to conventional treatments.Given the high fraction dose, highly conformal dose distribution and steep dose gradient seen with SBRT, accurate target volume definition and dose delivery are crucial. The use of multiparametric (mp) magnetic resonance imaging (MRI) has improved target delineation for both the prostate and organs at risk, due to its superior soft-tissue contrast compared to computed tomography (CT) [9][10][11]. A previous randomized phase III study showed that focal ablative boosting to the mp-MRI visible tumor was feasible and not associated with increased toxicity up to two years after treatment [12].Prostate targeting accuracy based on position verification using fiducial marker imaging is high [13]. However, treatment of prostate cancer patients on a fully integrated MRI-linac system could increase https://doi.