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  • [Lancet Oncol.] Conventional versus hypofractionated high-dose intensity-modulated radiotherapy for prostate cancer: 5-year outcomes of the randomised, non-inferiority, phase 3 CHHiP trial.

    The Institute of Cancer Research / David Dearnaley*

  • 출처
    Lancet Oncol.
  • 등재일
    2016 Aug
  • 저널이슈번호
    17(8):1047-60. doi: 10.1016/S1470-2045(16)30102-4. Epub 2016 Jun 20.
  • 내용

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    Abstract

    BACKGROUND:

    Prostate cancer might have high radiation-fraction sensitivity that would give a therapeutic advantage to hypofractionated treatment. We present a pre-planned analysis of the efficacy and side-effects of a randomised trial comparing conventional and hypofractionated radiotherapy after 5 years follow-up.

     

    METHODS:

    CHHiP is a randomised, phase 3, non-inferiority trial that recruited men with localised prostate cancer (pT1b-T3aN0M0). Patients were randomly assigned (1:1:1) to conventional (74 Gy delivered in 37 fractions over 7·4 weeks) or one of two hypofractionated schedules (60 Gy in 20 fractions over 4 weeks or 57 Gy in 19 fractions over 3·8 weeks) all delivered with intensity-modulated techniques. Most patients were given radiotherapy with 3-6 months of neoadjuvant and concurrent androgen suppression. Randomisation was by computer-generated random permuted blocks, stratified by National Comprehensive Cancer Network (NCCN) risk group and radiotherapy treatment centre, and treatment allocation was not masked. The primary endpoint was time to biochemical or clinical failure; the critical hazard ratio (HR) for non-inferiority was 1·208. Analysis was by intention to treat. Long-term follow-up continues. The CHHiP trial is registered as an International Standard Randomised Controlled Trial, number ISRCTN97182923.

     

    FINDINGS:

    Between Oct 18, 2002, and June 17, 2011, 3216 men were enrolled from 71 centres and randomly assigned (74 Gy group, 1065 patients; 60 Gy group, 1074 patients; 57 Gy group, 1077 patients). Median follow-up was 62·4 months (IQR 53·9-77·0). The proportion of patients who were biochemical or clinical failure free at 5 years was 88·3% (95% CI 86·0-90·2) in the 74 Gy group, 90·6% (88·5-92·3) in the 60 Gy group, and 85·9% (83·4-88·0) in the 57 Gy group. 60 Gy was non-inferior to 74 Gy (HR 0·84 [90% CI 0·68-1·03], pNI=0·0018) but non-inferiority could not be claimed for 57 Gy compared with 74 Gy (HR 1·20 [0·99-1·46], pNI=0·48). Long-term side-effects were similar in the hypofractionated groups compared with the conventional group. There were no significant differences in either the proportion or cumulative incidence of side-effects 5 years after treatment using three clinician-reported as well as patient-reported outcome measures. The estimated cumulative 5 year incidence of Radiation Therapy Oncology Group (RTOG) grade 2 or worse bowel and bladder adverse events was 13·7% (111 events) and 9·1% (66 events) in the 74 Gy group, 11·9% (105 events) and 11·7% (88 events) in the 60 Gy group, 11·3% (95 events) and 6·6% (57 events) in the 57 Gy group, respectively. No treatment-related deaths were reported.

     

    INTERPRETATION:

    Hypofractionated radiotherapy using 60 Gy in 20 fractions is non-inferior to conventional fractionation using 74 Gy in 37 fractions and is recommended as a new standard of care for external-beam radiotherapy of localised prostate cancer.


    FUNDING:

    Cancer Research UK, Department of Health, and the National Institute for Health Research Cancer Research Network. 

     

    Author information

    Dearnaley D1, Syndikus I2, Mossop H3, Khoo V4, Birtle A5, Bloomfield D6, Graham J7, Kirkbride P8, Logue J9, Malik Z2, Money-Kyrle J10, O'Sullivan JM11, Panades M12, Parker C4, Patterson H13, Scrase C14, Staffurth J15, Stockdale A16, Tremlett J6, Bidmead M17, Mayles H2, Naismith O17, South C10, Gao A4, Cruickshank C3, Hassan S3, Pugh J3, Griffin C3, Hall E3; CHHiP Investigators.

    1The Institute of Cancer Research, London, UK; Royal Marsden NHS Foundation Trust, London, UK. Electronic address: David.Dearnaley@icr.ac.uk.

    2Clatterbridge Cancer Centre, Wirral, UK.

    3The Institute of Cancer Research, London, UK.

    4The Institute of Cancer Research, London, UK; Royal Marsden NHS Foundation Trust, London, UK.

    5Rosemere Cancer Centre, Royal Preston Hospital, Preston, UK.

    6Brighton and Sussex University Hospitals, Brighton, UK.

    7Beacon Centre, Musgrove Park Hospital, Taunton, UK.

    8Sheffield Teaching Hospitals Foundation Trust, Sheffield, UK.

    9Christie Hospital, Manchester, UK.

    10Royal Surrey County Hospital, Guildford, UK.

    11Queen's University Belfast, Belfast, UK.

    12Lincoln County Hospital, Lincoln, UK.

    13Addenbrooke's Hospital, Cambridge, UK.

    14Ipswich Hospital, Ipswich, UK.

    15Cardiff University/Velindre Cancer Centre, Cardiff, UK.

    16University Hospital Coventry, Coventry, UK.

    17Royal Marsden NHS Foundation Trust, London, UK.

     

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