Prognostic Value of Biochemical Recurrence Following Treatment with Curative Intent for Prostate Cancer: A Systematic Review.

Biochemical recurrence European Association of Urology Gleason score Guidelines PSA kinetics Prognostic factors Prostate cancer Radical prostatectomy Radiotherapy Systematic review

Journal

European urology
ISSN: 1873-7560
Titre abrégé: Eur Urol
Pays: Switzerland
ID NLM: 7512719

Informations de publication

Date de publication:
06 2019
Historique:
received: 25 06 2018
accepted: 03 10 2018
pubmed: 22 10 2018
medline: 24 7 2020
entrez: 22 10 2018
Statut: ppublish

Résumé

In men with prostate cancer (PCa) treated with curative intent, controversy exists regarding the impact of biochemical recurrence (BCR) on oncological outcomes. To perform a systematic review of the existing literature on BCR after treatment with curative intent for nonmetastatic PCa. Objective 1 is to investigate whether oncological outcomes differ between patients with or without BCR. Objective 2 is to study which clinical factors and tumor features in patients with BCR have an independent prognostic impact on oncological outcomes. Medline, Medline In-Process, Embase, and the Cochrane Central Register of Controlled Trials were searched. For objective 1, prospective and retrospective studies comparing survival outcomes of patients with or without BCR following radical prostatectomy (RP) or radical radiotherapy (RT) were included. For objective 2, all studies with at least 100 participants and reporting on prognostic patient and tumor characteristics in patients with BCR were included. Risk-of-bias and confounding assessments were performed according to the Quality in Prognosis Studies tool. Both a narrative synthesis and a meta-analysis were undertaken. Overall, 77 studies were included for analysis, of which 14 addressed objective 1, recruiting 20 406 patients. Objective 2 was addressed by 71 studies with 29 057, 11 301, and 4272 patients undergoing RP, RT, and a mixed population (mix of patients undergoing RP or RT as primary treatment), respectively. There was a low risk of bias for study participation, confounders, and statistical analysis. For most studies, attrition bias, and prognostic and outcome measurements were not clearly reported. BCR was associated with worse survival rates, mainly in patients with short prostate-specific antigen doubling time (PSA-DT) and a high final Gleason score after RP, or a short interval to biochemical failure (IBF) after RT and a high biopsy Gleason score. BCR has an impact on survival, but this effect appears to be limited to a subgroup of patients with specific clinical risk factors. Short PSA-DT and a high final Gleason score after RP, and a short IBF after RT and a high biopsy Gleason score are the main factors that have a negative impact on survival. These factors may form the basis of new BCR risk stratification (European Association of Urology BCR Risk Groups), which needs to be validated formally. This review looks at the risk of death in men who shows rising prostate-specific antigen (PSA) in the blood test performed after curative surgery or radiotherapy. For many men, rising PSA does not mean that they are at a high risk of death from prostate cancer in the longer term. Men with PSA that rises shortly after they were treated with radiotherapy or rapidly rising PSA after surgery and a high tumor grade for both treatment modalities are at the highest risk of death. These factors may form the basis of new risk stratification (European Association of Urology biochemical recurrence Risk Groups), which needs to be validated formally.

Identifiants

pubmed: 30342843
pii: S0302-2838(18)30752-8
doi: 10.1016/j.eururo.2018.10.011
pii:
doi:

Substances chimiques

KLK3 protein, human EC 3.4.21.-
Kallikreins EC 3.4.21.-
Prostate-Specific Antigen EC 3.4.21.77

Types de publication

Journal Article Review Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

967-987

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2018 European Association of Urology. Published by Elsevier B.V. All rights reserved.

Auteurs

Thomas Van den Broeck (T)

Department of Urology, University Hospitals Leuven, Leuven, Belgium; Laboratory of Molecular Endocrinology, KU Leuven, Leuven, Belgium. Electronic address: vandenbroeck.thomas@gmail.com.

Roderick C N van den Bergh (RCN)

Department of Urology, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Nicolas Arfi (N)

Department of Urology, Hospital Saint Luc Saint Joseph, Lyon, France.

Tobias Gross (T)

Department of Urology, University of Bern, Inselspital, Bern, Switzerland.

Lisa Moris (L)

Department of Urology, University Hospitals Leuven, Leuven, Belgium; Laboratory of Molecular Endocrinology, KU Leuven, Leuven, Belgium.

Erik Briers (E)

Hasselt, Belgium.

Marcus Cumberbatch (M)

Academic Urology Unit, University of Sheffield, Sheffield, UK.

Maria De Santis (M)

Charite Universitätsmedizin, Berlin, Germany; Department of Urology, Medical University of Vienna, Vienna, Austria.

Derya Tilki (D)

Martini-Klinik Prostate Cancer Center, University Hospital Hamburg-Eppendorf, Hamburg, Germany; Department of Urology, University Hospital Hamburg-Eppendorf, Hamburg, Germany.

Stefano Fanti (S)

Nuclear Medicine Division, Policlinico S. Orsola, University of Bologna, Italy.

Nicola Fossati (N)

Unit of Urology/Division of Oncology, URI, IRCCS Ospedale San Raffaele, Milan, Italy; Università Vita-Salute San Raffaele, Milan, Italy.

Silke Gillessen (S)

Division of Cancer Sciences, University of Manchester and The Christie, Manchester, UK; Department of Oncology and Haematology, Cantonal Hospital St Gallen, St Gallen, Switzerland; University of Bern, Bern, Switzerland.

Jeremy P Grummet (JP)

Department of Surgery, Central Clinical School, Monash University, Caulfield North, Victoria, Australia.

Ann M Henry (AM)

Leeds Cancer Centre, St. James's University Hospital and University of Leeds, Leeds, UK.

Michael Lardas (M)

Department of Urology, Leto Hospital, Athens, Greece.

Matthew Liew (M)

Department of Urology, Wrightington, Wigan and Leigh NHS Foundation Trust, Wigan, UK.

Olivier Rouvière (O)

Hospices Civils de Lyon, Radiology Department, Edouard Herriot Hospital, Lyon, France.

Jakub Pecanka (J)

Pecanka Consulting Services, Prague, Czech Republic; Department of Biomedical Data Sciences, University Medical Center, Leiden, The Netherlands.

Malcolm D Mason (MD)

Division of Cancer & Genetics, School of Medicine Cardiff University, Velindre Cancer Centre, Cardiff, UK.

Ivo G Schoots (IG)

Department of Radiology & Nuclear Medicine, Erasmus MC University Medical Center, Rotterdam, The Netherlands.

Theo H van Der Kwast (TH)

Department of Pathology, Erasmus Medical Centre, Rotterdam, The Netherlands.

Henk G van Der Poel (HG)

Department of Urology, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Thomas Wiegel (T)

Department of Radiation Oncology, University Hospital Ulm, Ulm, Germany.

Peter-Paul M Willemse (PM)

Department of Urology, University Hospital Groningen, Groningen, The Netherlands.

Yuhong Yuan (Y)

Department of Medicine, McMaster University, Hamilton, ON, Canada.

Thomas B Lam (TB)

Academic Urology Unit, University of Aberdeen, Aberdeen, UK; Department of Urology, Aberdeen Royal Infirmary, Aberdeen, UK.

Philip Cornford (P)

Royal Liverpool and Broadgreen Hospitals NHS Trust, Liverpool, UK.

Nicolas Mottet (N)

Department of Urology, University Hospital, St. Etienne, France.

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