{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,1]],"date-time":"2026-10-01T08:50:27Z","timestamp":1790844627653,"version":"4.1.0"},"reference-count":29,"publisher":"Wiley","license":[{"start":{"date-parts":[[2026,9,18]],"date-time":"2026-09-18T00:00:00Z","timestamp":1789689600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"},{"start":{"date-parts":[[2026,9,18]],"date-time":"2026-09-18T00:00:00Z","timestamp":1789689600000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"funder":[{"DOI":"10.13039\/501100000664","name":"Health Technology Assessment Programme","doi-asserted-by":"publisher","award":["17\/150\/01"],"award-info":[{"award-number":["17\/150\/01"]}],"id":[{"id":"10.13039\/501100000664","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["bjui-journals.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["BJU International"],"abstract":"<jats:sec>\n                    <jats:title>Objectives<\/jats:title>\n                    <jats:p>Primary objective: to determine whether prostate gland partial ablation (PA) has non\u2010inferior oncological treatment success vs radical treatment (RT) of localised intermediate\u2010risk prostate cancer (irPCa). Secondary objectives: to compare (i) participant\u2010reported urinary and sexual dysfunction side effects, (ii) short\/medium term serious adverse events, (iii) health\u2010related quality of life (HRQoL), (iv) cost\u2010effectiveness; and to report (v) the need for repeat PA, (vi) accuracy of magnetic resonance imaging and biopsy protocols in determining suitability for PA, (vii) disease progression, local spread and metastases, (viii) medium\u2010term disease\u2010specific and overall mortality.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Participants and Methods<\/jats:title>\n                    <jats:p>The \u2018Partial prostate Ablation versus Radical Treatment\u2019 (PART; International Standard Randomised Controlled Trial Number ISRCTN17249875) is a UK\u2010wide, multicentre, pragmatic, randomised controlled trial investigating whether PA (high\u2010intensity focused ultrasound [HIFU] or irreversible electroporation [IRE]) is non\u2010inferior to RT (radical prostatectomy, radical radiotherapy, or low\u2010dose\u2010rate brachytherapy [LDR\u2010B]) in treating localised irPCa. A Qualitative Research Integrated within Trials (QuinteT) Recruitment Intervention is included to optimise recruitment and informed consent. Primary outcome treatment success for PA will be determined by prostate biopsies and imaging, and for RT using standard definitions. Participants will receive treatment according to their randomised allocation, with HIFU or IRE for PA depending on lesion location, and radical prostatectomy, radical radiotherapy, or LDR\u2010B according to patient and physician preference for RT. Based on 95% and 85% oncological treatment success for RT and PA, respectively, with a non\u2010inferiority margin of 20%, at median 3\u2009years of follow\u2010up, PART requires 275 recruited men (137 per group, randomised on a 1:1 basis), for 80% power, with a one\u2010sided alpha of 0.025. Allowing for a 10% total withdrawal or dropout rate, PART requires 306 recruited and randomised participants.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>The PART trial will provide robust prospective data and high\u2010level randomised evidence to determine oncological treatment effectiveness of PA vs RT for localised irPCa, along with comparative side effect, HRQoL, and health economics evaluations, to inform clinical decision\u2010making.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/bju.70448","type":"journal-article","created":{"date-parts":[[2026,9,19]],"date-time":"2026-09-19T00:50:16Z","timestamp":1789779016000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":1,"title":["The\n                    <scp>PART<\/scp>\n                    randomised trial protocol: Partial Ablation versus Radical Treatment for prostate cancer"],"prefix":"10.1111","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-8330-9251","authenticated-orcid":false,"given":"Richard J.","family":"Bryant","sequence":"first","affiliation":[{"name":"Department of Urology, Churchill Hospital Oxford University Hospitals NHS Foundation Trust  Oxford UK"},{"name":"Nuffield Department of Surgical Sciences University of Oxford  Oxford UK"},{"name":"Surgical Intervention Trials Unit University of Oxford  Oxford UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-4155-1840","authenticated-orcid":false,"given":"Tom","family":"Leslie","sequence":"additional","affiliation":[{"name":"Department of Urology, Churchill Hospital Oxford University Hospitals NHS Foundation Trust  Oxford UK"},{"name":"Nuffield Department of Surgical Sciences University of Oxford  Oxford 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