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dc.contributor.authorKass-Iliyya, A
dc.contributor.authorJovic, G
dc.contributor.authorMurphy, C
dc.contributor.authorFisher, C
dc.contributor.authorSyndikus, I
dc.contributor.authorJose, C
dc.contributor.authorScrase, CD
dc.contributor.authorGraham, JD
dc.contributor.authorNicol, D
dc.contributor.authorSydes, MR
dc.contributor.authorDearnaley, D
dc.date.accessioned2018-03-01T14:43:53Z
dc.date.issued2018-06-01
dc.identifier.citationEuropean urology, 2018, 73 (6), pp. 968 - 976
dc.identifier.issn0302-2838
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/1470
dc.identifier.eissn1873-7560
dc.identifier.doi10.1016/j.eururo.2017.12.017
dc.description.abstractBACKGROUND: The importance of 2-yr postradiotherapy prostate biopsy status remains uncertain. OBJECTIVE: To assess the value of 2 year post treatment biopsies in a randomised trial of radiotherapy dose escalation. DESIGN, SETTING, AND PARTICIPANTS: Between 1998 and 2001, 843 men with localised prostate cancer were randomised to receive either control-64Gy or escalated-74Gy conformal radiotherapy (CFRT) in the MRC RT01 trial in combination with 3-6-mo neoadjuvant androgen deprivation therapy. Prostate biopsies were planned at 2 yr from start of CFRT in suitable men. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: Prostate biopsy results and prostate-specific antigen (PSA) levels performed at 2 yr post-CFRT were evaluated with long-term biochemical progression free survival (bPFS) and overall survival. Outcome measures were timed from the 2-yr biopsy using a landmark approach. RESULTS AND LIMITATIONS: A 2-yr biopsy was performed in 312/843 patients. One hundred and seventy-seven patients were included in the per-protocol group with median follow-up of 7.8 yr from biopsy. Median PSA at biopsy was 0.5ng/ml. Sixty-four bPFS events were reported: 46/145 (32%) in patients with negative, 6/18 (33%) suspicious, and 12/14 (86%) positive biopsies. A positive biopsy was prognostic of worse bPFS, going forward, compared with negative and suspicious biopsies, hazard ratio (HR)=4.81 (95% confidence interval [CI]: 2.50-9.26, p<0.001). The estimate for survival was HR=1.58 (95% CI: 0.52-4.78, p=0.42). PSA values at 2 yr between 1.01ng/ml and 2.09ng/ml were also associated with subsequent PSA failures (HR=2.71, 95% CI: 1.98-3.71), bPFS events (HR=2.45, 95% CI: 1.81-3.32), and prostate cancer-specific survival (HR=2.87, 95% CI: 1.08-7.64) compared with PSA ≤1.0ng/ml. CONCLUSIONS: Two-year postradiotherapy prostate biopsies have limited value in patients with PSA control but both positive biopsy and higher PSA status are strongly associated with future bPFS events. A policy of selected biopsy may provide an opportunity for early salvage interventions. PATIENT SUMMARY: Routine 2-yr postradiotherapy biopsy is not recommended but can be considered in selected patients with unfavourable post-treatment prostate-specific antigen levels who are suitable for early salvage treatments.
dc.formatPrint-Electronic
dc.format.extent968 - 976
dc.languageeng
dc.language.isoeng
dc.publisherELSEVIER SCIENCE BV
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectProstate
dc.subjectHumans
dc.subjectProstatic Neoplasms
dc.subjectAndrogen Antagonists
dc.subjectProstate-Specific Antigen
dc.subjectBiopsy
dc.subjectNeoadjuvant Therapy
dc.subjectRadiotherapy Dosage
dc.subjectSurvival Rate
dc.subjectFollow-Up Studies
dc.subjectAged
dc.subjectMiddle Aged
dc.subjectMale
dc.subjectRandomized Controlled Trials as Topic
dc.subjectProgression-Free Survival
dc.titleTwo-years Postradiotherapy Biopsies: Lessons from MRC RT01 Trial.
dc.typeJournal Article
dcterms.dateAccepted2017-12-14
rioxxterms.versionofrecord10.1016/j.eururo.2017.12.017
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2018-06
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfEuropean urology
pubs.issue6
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/Closed research teams
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Closed research teams/Clinical Academic Radiotherapy (Dearnaley)
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/Closed research teams
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Closed research teams/Clinical Academic Radiotherapy (Dearnaley)
pubs.publication-statusPublished
pubs.volume73
pubs.embargo.termsNot known
icr.researchteamClinical Academic Radiotherapy (Dearnaley)
dc.contributor.icrauthorDearnaley, David


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