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

Thomas Van den Broeck*, Roderick C.N. van den Bergh, Nicolas Arfi, Tobias Gross, Lisa Moris, Erik Briers, Marcus Cumberbatch, Maria De Santis, Derya Tilki, Stefano Fanti, Nicola Fossati, Silke Gillessen, Jeremy P. Grummet, Ann M. Henry, Michael Lardas, Matthew Liew, Olivier Rouvière, Jakub Pecanka, Malcolm D. Mason, Ivo G. SchootsTheo H. van Der Kwast, Henk G. van Der Poel, Thomas Wiegel, Peter Paul M. Willemse, Yuhong Yuan, Thomas B. Lam, Philip Cornford, Nicolas Mottet

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

276 Citations (Scopus)

Abstract

Context: In men with prostate cancer (PCa) treated with curative intent, controversy exists regarding the impact of biochemical recurrence (BCR) on oncological outcomes. Objective: 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. Evidence acquisition: 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. Evidence synthesis: 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. Conclusions: 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. Patient summary: 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. In patients who underwent radical prostatectomy as primary treatment and who subsequently developed biochemical recurrence (BCR), the main prognostic factor for distant metastases, prostate cancer-specific mortality, and overall mortality is short prostate-specific antigen doubling time (ie, <1 yr), and to a lesser extent an increasing pathological Gleason score (GS) and a short interval to biochemical failure (IBF). The main prognostic factors for patients developing BCR following primary radiotherapy are a short IBF (<18 mo) and to a lesser extent an increasing biopsy GS.

Original languageEnglish
Pages (from-to)967-987
Number of pages21
JournalEuropean Urology
Volume75
Issue number6
Early online date17 Oct 2018
DOIs
Publication statusPublished - Jun 2019

Bibliographical note

Funding Information:
Financial disclosures: Thomas Van den Broeck certifies that all conflicts of interest, including specific financial interests and relationships and affiliations relevant to the subject matter or materials discussed in the manuscript (eg, employment/affiliation, grants or funding, consultancies, honoraria, stock ownership or options, expert testimony, royalties, or patents filed, received, or pending), are the following: Professor Dr. H.G. van Der Poel is a company consultant for Intuitive Surgical, has participated in trials for Astellas and Steba Biotech, and has received grant and research support from Astellas. P. Cornford is a company consultant for Astellas, Ipsen, and Ferring; receives company speaker honoraria from Astellas, Janssen, Ipsen, and Pfizer; participates in trials from Ferring; and receives fellowships and travel grants from Astellas and Janssen. T.B. Lam is a company consultant for and has received company speaker honoraria from Pfizer, GSK, Astellas, and Ipsen. Professor Dr. A.M. Henry is a company consultant for Nucletron-Elektra; participates in trials by Cancer Research UK and the National Institute of Health Research (UK); received travel grants from the Medical Research Council, the National Institute of Health Research (UK), and Cancer Research UK; and received research grants from Cancer Research UK and the Sir John Fisher Foundation. Professor Dr. M.D. Mason is a company consultant for Ellipses Pharma and Oncotherics. Professor Dr. T. Wiegel is a member of the advisory board for IPSEN, receives company speaker honorarium from IPSEN and Hexal, is a member of the Janssen Steering Committee, and has participated in the ATLAS/AUO trial. Professor Dr. S. Gillessen is a company consultant for AAA International, Astellas Pharma, Bayer, Bristol-Myers Squibb, Clovis, CureVac, Ferring, Innocrin Pharmaceuticals, Janssen Cilag, MaxIVAX SA, Orion, Roche, Sanofi Aventis Group, Nectar, and ProteoMediX; received speaker honorarium from Janssen and Novartis; and participates in multiple trials from different companies. O. Rouvière received company speaker honorarium from EDAP-TMS, participates in trials by ESAO-TMS and Vermon, and received research and travel grants from Philips. M. De Santis is a company consultant for Amgen, Astellas, AstraZeneca, Bayer, Birsto-Myers Squibb, Celgene, Dendreon, Eisai Inc., ESSA, Ferring, GSK, Incyte, IPSEN, Janssen Cilag, Merck, MSD, Novartis, Pfizer, Piere Fabre Oncologie, Roche, Sanofi Aventis, SeaGen, Shionogi, Synthon, Takeda, Teva, OncoGenex, and Sandoz; receives speaker honorarium from Amgen, Astellas, AstraZeneca, Bayer, Birstol-Kyers Squibb, Ferring, GSK, IPSEN, Janssen Cilag, Merck, MSD, Novartis, Pfizer, Pierre Fabre Oncologie, Roche, Sanofi Aventis, Synthon, and Takeda; participates in trials by the Technical University Munich, Amgen, Astellas, AstraZeneca, Bayer, Bristol-Myers Squivv, Celgene, Dendreon, Eisai Inc, Ferring, GSK, IPSEN, Incyte, Janssen Cilag, Merck, MSD, Novartis, Pfizer, Pierre Fabre Oncologie, Roche, Sanofi Aventis, and SOTIO; participates in various trials as a member of the EORTC GU group; received research grants from Pierre Fabre Oncologie and travel grants from Amgen, Astellas, AstraZeneca, Bayer, Bristol-Myers Squivv, Celgene, Dendreaon, Ferring, GSK, IPSEN, Incyte, Janssen Cilag, Merck, MSD, Novartis, Pfizer, Pierre Fabre Oncologie, Roche, Sanofi Aventis, SeaGen, Shionogi, Synthon, Takeda, and Teva/OncoGenex. Professor Dr. D. Tilki is a company consultant for Steba Biotech and MDx Health; has received speaker honorarium from Mundipharma, Astellas, and Ribosepharm; participates in trials by MDxHealth; received travel and research grants from Janssen; and is a member of the PIONEER consortium. Professor Dr. S. Fanti is a company consultant for Bayer and ANMI; has received speaker honorarium from Bayer, Genzyme, ANMI, and GE Healthcare; and participates in trials by Amgen, Bayer, BMS, Genzyme, Janssen, Merck, and Novartis. Professor Dr. N. Mottet is a company consultant for Janssen, GE, BMS, Sanofi, and Astellas; has received speaker honorarium from Astellas, Pierre Fabre, Steba, Janssen, and Ferring; and received fellowships and travel grants from Astellas, IPSEN, Sanofi, Janssen, and Roche. Dr. T. Van den Broeck, Dr. R.C.N. van den Bergh, Dr. N. Arfi, Dr. L. Moris, Dr. E. Briers, Mr. M. Cumberbatch, Dr. N. Fossati, Professor Dr. J.P. Grummet, Dr. M. Lardas, Mr. M. Liew, Dr. J. Pecanka, Dr. I.G. Schoots, Dr. P.P.M. Willemse, Dr. Y. Yuan, and Professor Dr. T.H. Van Der Kwast have nothing to disclose.

Publisher Copyright:
© 2018 European Association of Urology

Keywords

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

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