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    Timing of radiotherapy (RT) after radical prostatectomy (RP): long-term outcomes in the RADICALS-RT trial (NCT00541047)

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    Authors
    Parker, C. C.
    Petersen, P. M.
    Cook, A. D.
    Clarke, Noel W
    Catton, C.
    Cross, W. R.
    Kynaston, H.
    Parulekar, W. R.
    Persad, R. A.
    Saad, F.
    Bower, L.
    Durkan, G. C.
    Logue, John
    Maniatis, C.
    Noor, D.
    Payne, H.
    Anderson, J.
    Bahl, A. K.
    Bashir, F.
    Bottomley, D. M.
    Brasso, K.
    Capaldi, L.
    Chung, C.
    Cooke, P. W.
    Donohue, J. F.
    Eddy, B.
    Heath, C. M.
    Henderson, A.
    Henry, A.
    Jaganathan, R.
    Jakobsen, H.
    James, N. D.
    Joseph, J.
    Lees, K.
    Lester, J.
    Lindberg, H.
    Makar, A.
    Morris, S. L.
    Oommen, N.
    Ostler, P.
    Owen, L.
    Patel, P.
    Pope, A.
    Popert, R.
    Raman, R.
    Ramani, V.
    Røder, A.
    Sayers, I.
    Simms, M.
    Srinivasan, V.
    Sundaram, S.
    Tarver, K. L.
    Tran, A.
    Wells, P.
    Wilson, J.
    Zarkar, A. M.
    Parmar, M. K. B.
    Sydes, M. R.
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    Affiliation
    Department of Urology, The Christie NHS Foundation Trust, Manchester; Manchester Cancer Research Centre, The University of Manchester, Manchester
    Issue Date
    2024
    
    Metadata
    Show full item record
    Abstract
    BACKGROUND: 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. PATIENTS AND METHODS: 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 fractions) and treatment centre. The primary outcome measure was freedom-from-distant-metastasis (FFDM), designed with 80% power to detect an improvement from 90% with Salvage-RT (control) to 95% at 10 years with Adjuvant-RT. Secondary outcome measures were biochemical progression-free survival, freedom from non-protocol hormone therapy, safety and patient-reported outcomes. Standard survival analysis methods were used; hazard ratio (HR)<1 favours Adjuvant-RT. RESULTS: Between October 2007 and December 2016, 1396 participants from UK, Denmark, Canada and Ireland were randomised: 699 Salvage-RT, 697 Adjuvant-RT. Allocated groups were balanced with a median age of 65 years. Ninety-three percent (649/697) Adjuvant-RT reported RT within 6 months after randomisation; 39% (270/699) Salvage-RT reported RT during follow-up. Median follow-up was 7.8 years. With 80 distant metastasis events, 10-year FFDM was 93% for Adjuvant-RT and 90% for Salvage-RT: HR=0.68 [95% confidence interval (CI) 0.43-1.07, P=0.095]. Of 109 deaths, 17 were due to prostate cancer. Overall survival was not improved (HR=0.980, 95% CI 0.667-1.440, P=0.917). Adjuvant-RT reported worse urinary and faecal incontinence 1 year after randomisation (P=0.001); faecal incontinence remained significant after 10 years (P=0.017). CONCLUSION: Long-term results from RADICALS-RT confirm adjuvant RT after radical prostatectomy increases the risk of urinary and bowel morbidity, but does not meaningfully improve disease control. An observation policy with salvage RT for PSA failure should be the current standard after radical prostatectomy. TRIAL IDENTIFICATION: RADICALS, RADICALS-RT, ISRCTN40814031, NCT00541047.
    Citation
    Parker CC, Petersen PM, Cook AD, Clarke NW, Catton C, Cross WR, et al. Timing of radiotherapy (RT) after radical prostatectomy (RP): long-term outcomes in the RADICALS-RT trial (NCT00541047). Annals of oncology : official journal of the European Society for Medical Oncology. 2024 Jul;35(7):656-66. PubMed PMID: 38583574. Epub 2024/04/08. eng.
    Journal
    Annals of Oncology
    URI
    http://hdl.handle.net/10541/627054
    DOI
    10.1016/j.annonc.2024.03.010
    PubMed ID
    38583574
    Additional Links
    https://dx.doi.org/10.1016/j.annonc.2024.03.010
    Type
    Article
    Language
    en
    ae974a485f413a2113503eed53cd6c53
    10.1016/j.annonc.2024.03.010
    Scopus Count
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