Evidence map›Paper›PMID 31767473›Full record

Trial reportRadiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology2020

A randomised assessment of image guided radiotherapy within a phase 3 trial of conventional or hypofractionated high dose intensity modulated radiotherapy for prostate cancer.

Julia Murray, Clare Griffin, Sarah Gulliford, Isabel Syndikus, John Staffurth, Miguel Panades, Christopher Scrase, Chris Parker, Vincent Khoo, Jamie Dean and 10 more

Abstract readClinical Trial, Phase IIIRandomized Controlled TrialEquivalence Trial
In one paragraph

Trial report in Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
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  5. Impact of image-guided radiation therapy with intraprostatic seeds on long-term toxicity in prostate cancer patients undergoing risk-adapted intensification therapy.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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  7. [Comparison of setup errors between two immobilization methods in prostate cancer radiotherapy based on cone-beam computed tomography].Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences · 2025
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  12. Review
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  16. Tomotherapy-based moderate hypofractionation for localized prostate cancer: a mono-institutional analysis.Reports of practical oncology and radiotherapy : journal of Greatpoland Cancer Center in Poznan and Polish Society of Radiation Oncology · 2022
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors.

Julia MurrayThe Institute of Cancer Research, London, UK; Royal Marsden NHS Foundation Trust, London, UK.
Clare GriffinThe Institute of Cancer Research, London, UK.
Sarah GullifordThe Institute of Cancer Research, London, UK; Department of Radiotherapy, University College London Hospitals NHS Foundation Trust, UK.
Isabel SyndikusClatterbridge Cancer Centre, Wirral, UK.
John StaffurthCardiff University/Velindre Cancer Centre, UK.
Miguel PanadesLincoln County Hospital, UK.
Christopher ScraseIpswich Hospital, UK.
Chris ParkerThe Institute of Cancer Research, London, UK; Royal Marsden NHS Foundation Trust, London, UK.
Vincent KhooThe Institute of Cancer Research, London, UK; Royal Marsden NHS Foundation Trust, London, UK.
Jamie DeanThe Institute of Cancer Research, London, UK.
Helen MaylesClatterbridge Cancer Centre, Wirral, UK.
Philip MaylesClatterbridge Cancer Centre, Wirral, UK.
Simon ThomasAddenbrooke's Hospital, Cambridge, UK.
Olivia NaismithRoyal Marsden NHS Foundation Trust, London, UK.
Angela BakerRoyal Berkshire Hospital, Reading, UK.
Helen MossopThe Institute of Cancer Research, London, UK.
Clare CruickshankThe Institute of Cancer Research, London, UK.
Emma HallThe Institute of Cancer Research, London, UK.
David DearnaleyThe Institute of Cancer Research, London, UK; Royal Marsden NHS Foundation Trust, London, UK. Electronic address: david.dearnaley@icr.ac.uk.
CHHiP Investigators

Funding

Cancer Research UK 10588Cancer Research UK 12518Cancer Research UK 28284Cancer Research UK 7253Cancer Research UK C1491/A15955Cancer Research UK C1491/A9895Cancer Research UK C8262/A7253Cancer Research UK SP2312/021Department of Health
6 · The paper itself

Abstract

background and purposeImage-guided radiotherapy (IGRT) improves treatment set-up accuracy and provides the opportunity to reduce target volume margins. We introduced IGRT methods using standard (IGRT-S) or reduced (IGRT-R) margins in a randomised phase 2 substudy within CHHiP trial. We present a pre-planned analysis of the impact of IGRT on dosimetry and acute/late pelvic side effects using gastrointestinal and genitourinary clinician and patient-reported outcomes (PRO) and evaluate efficacy. MATERIALS AND

methodsCHHiP is a randomised phase 3, non-inferiority trial for men with localised prostate cancer. 3216 patients were randomly assigned to conventional (74 Gy in 2 Gy/fraction (f) daily) or moderate hypofractionation (60 or 57 Gy in 3 Gy/f daily) between October 2002 and June 2011. The IGRT substudy included a second randomisation assigning to no-IGRT, IGRT-S (standard CTV-PTV margins), or IGRT-R (reduced CTV-PTV margins). Primary substudy endpoint was late RTOG bowel and urinary toxicity at 2 years post-radiotherapy.

resultsBetween June 2010 to July 2011, 293 men were recruited from 16 centres. Median follow-up is 56.9(IQR 54.3-60.9) months. Rectal and bladder dose-volume and surface percentages were significantly lower in IGRT-R compared to IGRT-S group; (p < 0.0001). Cumulative proportion with RTOG grade ≥ 2 toxicity reported to 2 years for bowel was 8.3(95% CI 3.2-20.7)%, 8.3(4.7-14.6)% and 5.8(2.6-12.4)% and for urinary 8.4(3.2-20.8)%, 4.6(2.1-9.9)% and 3.9(1.5-9.9)% in no IGRT, IGRT-S and IGRT-R groups respectively. In an exploratory analysis, treatment efficacy appeared similar in all three groups.

conclusionIntroduction of IGRT was feasible in a national randomised trial and IGRT-R produced dosimetric benefits. Overall side effect profiles were acceptable in all groups but lowest with IGRT and reduced margins. ISRCTN: 97182923.

Indexed as

AgedAged, 80 and overFiducial MarkersHumansMaleMiddle AgedNeoplasm StagingPatient Reported Outcome MeasuresProstatic NeoplasmsRadiation Dose HypofractionationRadiotherapy, Image-GuidedRadiotherapy, Intensity-ModulatedRadiotherapy Planning, Computer-AssistedRectumDosimetryImage-guided radiotherapyProstateToxicity

Identifiers

PMID31767473
PMCPMC7005673

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.