<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Parker CC</submitter><funding>Cancer Research Campaign</funding><funding>Cancer Research UK</funding><funding>Canadian Cancer Society</funding><funding>UKRI Medical Research Council</funding><funding>Medical Research Council</funding><pagination>656-666</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7617161</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>35(7)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The optimal timing of radiotherapy (RT) after radical prostatectomy for prostate cancer has been uncertain. RADICALS-RT compared efficacy and safety of adjuvant RT versus an observation policy with salvage RT for prostate-specific antigen (PSA) failure.&lt;h4>Patients and methods&lt;/h4>RADICALS-RT was a randomised controlled trial enrolling patients with ≥1 risk factor (pT3/4, Gleason 7-10, positive margins, preoperative PSA≥10 ng/ml) for recurrence after radical prostatectomy. Patients were randomised 1:1 to adjuvant RT ('Adjuvant-RT') or an observation policy with salvage RT for PSA failure ('Salvage-RT') defined as PSA≥0.1 ng/ml or three consecutive rises. Stratification factors were Gleason score, margin status, planned RT schedule (52.5 Gy/20 fractions or 66 Gy/33 fracti</pubmed_abstract><journal>Annals of oncology : official journal of the European Society for Medical Oncology</journal><pubmed_title>Timing of radiotherapy (RT) after radical prostatectomy (RP): long-term outcomes in the RADICALS-RT trial (NCT00541047).</pubmed_title><pmcid>PMC7617161</pmcid><funding_grant_id>MC_UU_12023/28</funding_grant_id><funding_grant_id>MC_UU_00004/02</funding_grant_id><funding_grant_id>6381</funding_grant_id><pubmed_authors>Kynaston H</pubmed_authors><pubmed_authors>Sundaram S</pubmed_authors><pubmed_authors>Wells P</pubmed_authors><pubmed_authors>Wilson J</pubmed_authors><pubmed_authors>Bahl AK</pubmed_authors><pubmed_authors>Parmar MKB</pubmed_authors><pubmed_authors>Brasso K</pubmed_authors><pubmed_authors>Morris SL</pubmed_authors><pubmed_authors>Simms M</pubmed_authors><pubmed_authors>Patel P</pubmed_authors><pubmed_authors>Owen L</pubmed_authors><pubmed_authors>Lees K</pubmed_authors><pubmed_authors>Makar A</pubmed_authors><pubmed_authors>Pope A</pubmed_authors><pubmed_authors>Cook AD</pubmed_authors><pubmed_authors>Jaganathan R</pubmed_authors><pubmed_authors>James ND</pubmed_authors><pubmed_authors>Clarke NW</pubmed_authors><pubmed_authors>Lester J</pubmed_authors><pubmed_authors>Tarver KL</pubmed_authors><pubmed_authors>Zarkar AM</pubmed_authors><pubmed_authors>Cross WR</pubmed_authors><pubmed_authors>Ramani V</pubmed_authors><pubmed_authors>Cooke PW</pubmed_authors><pubmed_authors>Oommen N</pubmed_authors><pubmed_authors>Henderson A</pubmed_authors><pubmed_authors>Lindberg H</pubmed_authors><pubmed_authors>Bower L</pubmed_authors><pubmed_authors>Noor D</pubmed_authors><pubmed_authors>Henry A</pubmed_authors><pubmed_authors>Jakobsen H</pubmed_authors><pubmed_authors>Sydes MR</pubmed_authors><pubmed_authors>Donohue JF</pubmed_authors><pubmed_authors>Saad F</pubmed_authors><pubmed_authors>Capaldi L</pubmed_authors><pubmed_authors>RADICALS investigators</pubmed_authors><pubmed_authors>Eddy B</pubmed_authors><pubmed_authors>Sayers I</pubmed_authors><pubmed_authors>Srinivasan V</pubmed_authors><pubmed_authors>Popert R</pubmed_authors><pubmed_authors>Maniatis C</pubmed_authors><pubmed_authors>Petersen PM</pubmed_authors><pubmed_authors>Ostler P</pubmed_authors><pubmed_authors>Tran A</pubmed_authors><pubmed_authors>Roder A</pubmed_authors><pubmed_authors>Bottomley DM</pubmed_authors><pubmed_authors>Raman R</pubmed_authors><pubmed_authors>Parulekar WR</pubmed_authors><pubmed_authors>Heath CM</pubmed_authors><pubmed_authors>Anderson J</pubmed_authors><pubmed_authors>Bashir F</pubmed_authors><pubmed_authors>Chung C</pubmed_authors><pubmed_authors>Payne H</pubmed_authors><pubmed_authors>Joseph J</pubmed_authors><pubmed_authors>Catton C</pubmed_authors><pubmed_authors>Persad RA</pubmed_authors><pubmed_authors>Durkan GC</pubmed_authors><pubmed_authors>Logue J</pubmed_authors><pubmed_authors>Parker CC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Timing of radiotherapy (RT) after radical prostatectomy (RP): long-term outcomes in the RADICALS-RT trial (NCT00541047).</name><description>&lt;h4>Background&lt;/h4>The optimal timing of radiotherapy (RT) after radical prostatectomy for prostate cancer has been uncertain. RADICALS-RT compared efficacy and safety of adjuvant RT versus an observation policy with salvage RT for prostate-specific antigen (PSA) failure.&lt;h4>Patients and methods&lt;/h4>RADICALS-RT was a randomised controlled trial enrolling patients with ≥1 risk factor (pT3/4, Gleason 7-10, positive margins, preoperative PSA≥10 ng/ml) for recurrence after radical prostatectomy. Patients were randomised 1:1 to adjuvant RT ('Adjuvant-RT') or an observation policy with salvage RT for PSA failure ('Salvage-RT') defined as PSA≥0.1 ng/ml or three consecutive rises. Stratification factors were Gleason score, margin status, planned RT schedule (52.5 Gy/20 fractions or 66 Gy/33 fracti</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jul</publication><modification>2026-04-22T03:14:41.992Z</modification><creation>2025-04-06T22:21:03.794Z</creation></dates><accession>S-EPMC7617161</accession><cross_references><pubmed>38583574</pubmed><doi>10.1016/j.annonc.2024.03.010</doi></cross_references></HashMap>