Prostate‐specific antigen relapse‐free survival and side‐effects in 734 patients with up to 10 years of follow‐up with localized prostate cancer treated by permanent 125iodine implants
Abstract:Study Type – Therapy (case series) Level of Evidence 4
OBJECTIVE
To report our analysis of the oncological outcome, side‐effects and complications after 125I‐brachytherapy, based on 10 years of experience, as low dose‐rate (LDR) prostate brachytherapy is an accepted, effective and safe therapy for localized prostate cancer.
PATIENTS AND METHODS
Between April 1999 and December 2006, 734 consecutive patients were treated with clinically localized prostate cancer with a follow‐up of ≥30 months. No patients receiv… Show more
“…Relatively few single-center studies with a large and homogenous sample consisting of mostly low-risk patients have been reported (12,13). Moreover, of these large studies, few were European.…”
“…Relatively few single-center studies with a large and homogenous sample consisting of mostly low-risk patients have been reported (12,13). Moreover, of these large studies, few were European.…”
“…Institutional series using BT monotherapy support this finding [25,26]. Cosset EBRT plus BT as combination therapy has often been used (3, 14, [29-31]) but the additional benefit of combined EBRT over BT monotherapy remains unproven.…”
“…Shilkrut et al, retrospectively analyzed 958 high-risk PCa patients (PSA > 20 ng/ml; GS > 8; cT3-T4) treated with doseescalated EBRT (75)(76)(77)(78)(79)(80)(81) or combined EBRT/LDR-BRT, delivered with 103 Pd or 125 I [68]. ADT consisted of LH-RH analogue ± AA.…”
Section: Impact Of Adt On Clinical Outcomesmentioning
confidence: 99%
“…Almost all studies providing data on the role of combination ADT + BRT come from retrospective evaluations or retrospective secondary analysis of prospective trials with different primary endpoints (Table 4) [67][68][69][70][71][72][73][74][75][76][77][78][79][80][81][82]. Even if most of these analyses were adjusted for established PCa prognostic factors, evidence of the association between ADT and survival outcomes requires a prospective randomized trial in order to balance known and unknown prognostic between treatment arms, avoiding selection bias.…”
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