<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Gao LR</submitter><pubmed_abstract>&lt;h4>Objective&lt;/h4>To quantitatively characterize the dosimetric effects of long on-couch time in prostate cancer patients treated with adaptive ultra-hypofractionated radiotherapy (UHF-RT) on 1.5-Tesla magnetic resonance (MR)-linac.&lt;h4>Materials and methods&lt;/h4>Seventeen patients consecutively treated with UHF-RT on a 1.5-T MR-linac were recruited. A 36.25 Gy dose in five fractions was delivered every other day with a boost of 40 Gy to the whole prostate. We collected data for the following stages: pre-MR, position verification-MR (PV-MR) in the Adapt-To-Shape (ATS) workflow, and 3D-MR during the beam-on phase (Bn-MR) and at the end of RT (post-MR). The target and organ-at-risk contours in the PV-MR, Bn-MR, and post-MR stages were projected from the pre-MR data by deformable image registration and manually adapted by the physician, followed by dose recalculation for the ATS plan.&lt;h4>Results&lt;/h4>Overall, 290 MR scans were collected (85 pre-MR, 85 PV-MR, 49 Bn-MR and 71 post-MR scans). With a median on-couch time of 49 minutes, the mean planning target volume (PTV)-V&lt;sub>95%&lt;/sub> of all scans was 97.83 ± 0.13%. The corresponding mean clinical target volume (CTV)-V&lt;sub>100%&lt;/sub> was 99.93 ± 0.30%, 99.32 ± 1.20%, 98.59 ± 1.84%, and 98.69 ± 1.85%. With excellent prostate-V&lt;sub>100%&lt;/sub> dose coverage, the main reason for lower CTV-V&lt;sub>100%&lt;/sub> was slight underdosing of seminal vesicles (SVs). The median V&lt;sub>29 Gy&lt;/sub> change in the rectal wall was -1% (-20%-17%). The V&lt;sub>29 Gy&lt;/sub> of the rectal wall increased by >15% was observed in one scan. A slight increase in the high dose of bladder wall was noted due to gradual bladder growth during the workflow.&lt;h4>Conclusions&lt;/h4>This 3D-MR-based dosimetry analysis demonstrated clinically acceptable estimated dose coverage of target volumes during the beam-on period with adaptive ATS workflow on 1.5-T MR-linac, albeit with a relatively long on-couch time. The 3-mm CTV-PTV margin was adequate for prostate irradiation but occasionally insufficient for SVs. More attention should be paid to restricting high-dose RT to the rectal wall when optimizing the ATS plan.</pubmed_abstract><journal>Frontiers in oncology</journal><pagination>1039901</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9893501</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Assessment of delivered dose in prostate cancer patients treated with ultra-hypofractionated radiotherapy on 1.5-Tesla MR-Linac.</pubmed_title><pmcid>PMC9893501</pmcid><pubmed_authors>Gao LR</pubmed_authors><pubmed_authors>Fang H</pubmed_authors><pubmed_authors>Jing H</pubmed_authors><pubmed_authors>Wang MS</pubmed_authors><pubmed_authors>Song YW</pubmed_authors><pubmed_authors>Qi SN</pubmed_authors><pubmed_authors>Xing NZ</pubmed_authors><pubmed_authors>Chen B</pubmed_authors><pubmed_authors>Yan LL</pubmed_authors><pubmed_authors>Liu YP</pubmed_authors><pubmed_authors>Lu NN</pubmed_authors><pubmed_authors>Tian Y</pubmed_authors><pubmed_authors>Wang SL</pubmed_authors><pubmed_authors>Xia WL</pubmed_authors><pubmed_authors>Qin SR</pubmed_authors><pubmed_authors>Li YX</pubmed_authors><pubmed_authors>Tang Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Assessment of delivered dose in prostate cancer patients treated with ultra-hypofractionated radiotherapy on 1.5-Tesla MR-Linac.</name><description>&lt;h4>Objective&lt;/h4>To quantitatively characterize the dosimetric effects of long on-couch time in prostate cancer patients treated with adaptive ultra-hypofractionated radiotherapy (UHF-RT) on 1.5-Tesla magnetic resonance (MR)-linac.&lt;h4>Materials and methods&lt;/h4>Seventeen patients consecutively treated with UHF-RT on a 1.5-T MR-linac were recruited. A 36.25 Gy dose in five fractions was delivered every other day with a boost of 40 Gy to the whole prostate. We collected data for the following stages: pre-MR, position verification-MR (PV-MR) in the Adapt-To-Shape (ATS) workflow, and 3D-MR during the beam-on phase (Bn-MR) and at the end of RT (post-MR). The target and organ-at-risk contours in the PV-MR, Bn-MR, and post-MR stages were projected from the pre-MR data by deformable image registration and manually adapted by the physician, followed by dose recalculation for the ATS plan.&lt;h4>Results&lt;/h4>Overall, 290 MR scans were collected (85 pre-MR, 85 PV-MR, 49 Bn-MR and 71 post-MR scans). With a median on-couch time of 49 minutes, the mean planning target volume (PTV)-V&lt;sub>95%&lt;/sub> of all scans was 97.83 ± 0.13%. The corresponding mean clinical target volume (CTV)-V&lt;sub>100%&lt;/sub> was 99.93 ± 0.30%, 99.32 ± 1.20%, 98.59 ± 1.84%, and 98.69 ± 1.85%. With excellent prostate-V&lt;sub>100%&lt;/sub> dose coverage, the main reason for lower CTV-V&lt;sub>100%&lt;/sub> was slight underdosing of seminal vesicles (SVs). The median V&lt;sub>29 Gy&lt;/sub> change in the rectal wall was -1% (-20%-17%). The V&lt;sub>29 Gy&lt;/sub> of the rectal wall increased by >15% was observed in one scan. A slight increase in the high dose of bladder wall was noted due to gradual bladder growth during the workflow.&lt;h4>Conclusions&lt;/h4>This 3D-MR-based dosimetry analysis demonstrated clinically acceptable estimated dose coverage of target volumes during the beam-on period with adaptive ATS workflow on 1.5-T MR-linac, albeit with a relatively long on-couch time. The 3-mm CTV-PTV margin was adequate for prostate irradiation but occasionally insufficient for SVs. More attention should be paid to restricting high-dose RT to the rectal wall when optimizing the ATS plan.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023</publication><modification>2025-04-05T13:30:45.98Z</modification><creation>2025-04-05T13:30:45.98Z</creation></dates><accession>S-EPMC9893501</accession><cross_references><pubmed>36741014</pubmed><doi>10.3389/fonc.2023.1039901</doi></cross_references></HashMap>