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Docetaxel Versus Surveillance After Radical Prostatectomy for High-risk Prostate Cancer: Results from the Prospective Randomised, Open-label Phase 3 Scandinavian Prostate Cancer Group 12 Trial.
- Source :
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European urology [Eur Urol] 2018 Jun; Vol. 73 (6), pp. 870-876. Date of Electronic Publication: 2018 Feb 01. - Publication Year :
- 2018
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Abstract
- Background: Adjuvant chemotherapy is standard treatment for other solid tumours, but to date has not proven effective in prostate cancer.<br />Objective: o evaluate whether six cycles of docetaxel alone improve biochemical disease-free survival after radical prostatectomy for high-risk prostate cancer.<br />Design, Setting, and Participants: Open-label, randomised multinational phase 3 trial. Enrolment of 459 patients after prostatectomy.<br />Inclusion Criteria: high-risk pT2 margin positive or pT3a Gleason score ≥4+3, pT3b, or lymph node positive disease Gleason score ≥3+4. Patients assigned (1:1) to either six cycles of adjuvant docetaxel 75mg/m <superscript>2</superscript> every 3 wk without daily prednisone (Arm A) or surveillance (Arm B) until endpoint was reached. Primary endpoint was prostate-specific antigen progression ≥0.5 ng/ml.<br />Intervention: Docetaxel treatment after prostatectomy.<br />Results and Limitations: Median time to progression, death, or last follow-up was 56.8 mo. Primary endpoint was reached in 190/459 patients-the risk of progression at 5 yr being 41% (45% in Arm A and 38% in Arm B). There was evidence of nonproportional hazards in Kaplan-Meier analysis, so we used the difference in restricted mean survival time as the primary estimate of effect. Restricted mean survival time to endpoint was 43 mo in Arm A versus 46 mo in Arm B (p=0.06), a nonsignificant difference of 3.2 mo (95% confidence interval: 6.7 to -1.5 mo). A total of 116 serious adverse events were recorded in Arm A and 41 in Arm B with no treatment-related deaths. Not all patients received docetaxel by protocol. The endpoint is biochemical progression and some patients received radiation treatment before the endpoint.<br />Conclusions: Docetaxel without hormonal therapy did not significantly improve biochemical disease-free survival after radical prostatectomy.<br />Patient Summary: In this randomised trial, we tested whether chemotherapy after surgery for high-risk prostate cancer decreases the risk of a rising prostate-specific antigen. We found no benefit from docetaxel given after radical prostatectomy.<br /> (Copyright © 2018 European Association of Urology. Published by Elsevier B.V. All rights reserved.)
- Subjects :
- Aged
Antineoplastic Agents adverse effects
Chemotherapy, Adjuvant
Disease Progression
Disease-Free Survival
Docetaxel adverse effects
Humans
Lymphatic Metastasis
Male
Middle Aged
Neoplasm Grading
Neoplasm, Residual
Postoperative Period
Prospective Studies
Prostate-Specific Antigen blood
Prostatectomy adverse effects
Prostatic Neoplasms blood
Risk Factors
Survival Rate
Antineoplastic Agents therapeutic use
Docetaxel therapeutic use
Prostatic Neoplasms pathology
Prostatic Neoplasms therapy
Watchful Waiting
Subjects
Details
- Language :
- English
- ISSN :
- 1873-7560
- Volume :
- 73
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- European urology
- Publication Type :
- Academic Journal
- Accession number :
- 29395502
- Full Text :
- https://doi.org/10.1016/j.eururo.2018.01.012