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dc.contributor.authorBurdett, S
dc.contributor.authorBoevé, LM
dc.contributor.authorIngleby, FC
dc.contributor.authorFisher, DJ
dc.contributor.authorRydzewska, LH
dc.contributor.authorVale, CL
dc.contributor.authorvan Andel, G
dc.contributor.authorClarke, NW
dc.contributor.authorHulshof, MC
dc.contributor.authorJames, ND
dc.contributor.authorParker, CC
dc.contributor.authorParmar, MK
dc.contributor.authorSweeney, CJ
dc.contributor.authorSydes, MR
dc.contributor.authorTombal, B
dc.contributor.authorVerhagen, PC
dc.contributor.authorTierney, JF
dc.contributor.authorSTOPCAP M1 Radiotherapy Collaborators,
dc.date.accessioned2019-06-24T08:43:36Z
dc.date.issued2019-07-01
dc.identifier.citationEuropean urology, 2019, 76 (1), pp. 115 - 124
dc.identifier.issn0302-2838
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/3264
dc.identifier.eissn1873-7560
dc.identifier.doi10.1016/j.eururo.2019.02.003
dc.description.abstractBACKGROUND: Many trials are evaluating therapies for men with metastatic hormone-sensitive prostate cancer (mHSPC). OBJECTIVE: To systematically review trials of prostate radiotherapy. DESIGN, SETTING, AND PARTICIPANTS: Using a prospective framework (framework for adaptive meta-analysis [FAME]), we prespecified methods before any trial results were known. We searched extensively for eligible trials and asked investigators when results would be available. We could then anticipate that a definitive meta-analysis of the effects of prostate radiotherapy was possible. We obtained prepublication, unpublished, and harmonised results from investigators. INTERVENTION: We included trials that randomised men to prostate radiotherapy and androgen deprivation therapy (ADT) or ADT only. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: Hazard ratios (HRs) for the effects of prostate radiotherapy on survival, progression-free survival (PFS), failure-free survival (FFS), biochemical progression, and subgroup interactions were combined using fixed-effect meta-analysis. RESULTS AND LIMITATIONS: We identified one ongoing (PEACE-1) and two completed (HORRAD and STAMPEDE) eligible trials. Pooled results of the latter (2126 men; 90% of those eligible) showed no overall improvement in survival (HR=0.92, 95% confidence interval [CI] 0.81-1.04, p=0.195) or PFS (HR=0.94, 95% CI 0.84-1.05, p=0.238) with prostate radiotherapy. There was an overall improvement in biochemical progression (HR=0.74, 95% CI 0.67-0.82, p=0.94×10-8) and FFS (HR=0.76, 95% CI 0.69-0.84, p=0.64×10-7), equivalent to ∼10% benefit at 3yr. The effect of prostate radiotherapy varied by metastatic burden-a pattern consistent across trials and outcome measures, including survival (<5, ≥5; interaction HR=1.47, 95% CI 1.11-1.94, p=0.007). There was 7% improvement in 3-yr survival in men with fewer than five bone metastases. CONCLUSIONS: Prostate radiotherapy should be considered for men with mHSPC with a low metastatic burden. PATIENT SUMMARY: Prostate cancer that has spread to other parts of the body (metastases) is usually treated with hormone therapy. In men with fewer than five bone metastases, addition of prostate radiotherapy helped them live longer and should be considered.
dc.formatPrint-Electronic
dc.format.extent115 - 124
dc.languageeng
dc.language.isoeng
dc.publisherELSEVIER
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectSTOPCAP M1 Radiotherapy Collaborators
dc.subjectHumans
dc.subjectBone Neoplasms
dc.subjectProstatic Neoplasms
dc.subjectProstate-Specific Antigen
dc.subjectDisease-Free Survival
dc.subjectOrchiectomy
dc.subjectTumor Burden
dc.subjectSurvival Rate
dc.subjectMale
dc.subjectGonadotropin-Releasing Hormone
dc.subjectRandomized Controlled Trials as Topic
dc.subjectProgression-Free Survival
dc.titleProstate Radiotherapy for Metastatic Hormone-sensitive Prostate Cancer: A STOPCAP Systematic Review and Meta-analysis.
dc.typeJournal Article
dcterms.dateAccepted2019-02-05
rioxxterms.versionofrecord10.1016/j.eururo.2019.02.003
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2019-07
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfEuropean urology
pubs.issue1
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Prostate and Bladder Cancer Research
pubs.organisational-group/ICR/Primary Group/Royal Marsden Clinical Units
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Prostate and Bladder Cancer Research
pubs.organisational-group/ICR/Primary Group/Royal Marsden Clinical Units
pubs.publication-statusPublished
pubs.volume76
pubs.embargo.termsNot known
icr.researchteamProstate and Bladder Cancer Research
dc.contributor.icrauthorJames, Nicholas


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