Oncological outcomes of salvage radical prostatectomy for recurrent prostate cancer in the contemporary era: A multicenter retrospective study.


Journal

Urologic oncology
ISSN: 1873-2496
Titre abrégé: Urol Oncol
Pays: United States
ID NLM: 9805460

Informations de publication

Date de publication:
05 2021
Historique:
received: 15 07 2020
revised: 22 10 2020
accepted: 01 11 2020
pubmed: 14 1 2021
medline: 15 12 2021
entrez: 13 1 2021
Statut: ppublish

Résumé

Salvage radical prostatectomy (sRP) historically yields poor functional outcomes and high complication rates. However, recent reports on robotic sRP show improved results. Our objectives were to evaluate sRP oncological outcomes and predictors of positive margins and biochemical recurrence (BCR). We retrospectively collected data of sRP for recurrent prostate cancer after local nonsurgical treatment at 18 tertiary referral centers in United States, Australia and Europe, from 2000 to 2016. SM and BCR were evaluated in a univariate and multivariable analysis. Overall and cancer-specific survival were also assessed. We included 414 cases, 63.5% of them performed after radiotherapy. Before sRP the majority of patients had biopsy Gleason score (GS) ≤7 (55.5%) and imaging negative or with prostatic bed involvement only (93.3%). Final pathology showed aggressive histology in 39.7% (GS ≥9 27.6%), with 52.9% having ≥pT3 disease and 16% pN+. SM was positive in 29.7%. Five years BCR-Free, cancer-specific survival and OS were 56.7%, 97.7% and 92.1%, respectively. On multivariable analysis pathological T (pT3a odds ratio [OR] 2.939, 95% confidence interval [CI] 1.469-5.879; ≥pT3b OR 2.428-95% CI 1.333-4.423) and N stage (pN1 OR 2.871, 95% CI 1.503-5.897) were independent predictors of positive margins. Pathological T stage ≥T3b (OR 2.348 95% CI 1.338-4.117) and GS (up to OR 7.183, 95% CI 1.906-27.068 for GS >8) were independent predictors for BCR. Limitations include the retrospective nature of the study and limited follow-up. In a contemporary series, sRP showed promising oncological control in the medium term despite aggressive pathological features. BCR risk increased in case of locally advanced disease and higher GS. Future studies are needed to confirm our findings.

Sections du résumé

BACKGROUND
Salvage radical prostatectomy (sRP) historically yields poor functional outcomes and high complication rates. However, recent reports on robotic sRP show improved results. Our objectives were to evaluate sRP oncological outcomes and predictors of positive margins and biochemical recurrence (BCR).
METHODS
We retrospectively collected data of sRP for recurrent prostate cancer after local nonsurgical treatment at 18 tertiary referral centers in United States, Australia and Europe, from 2000 to 2016. SM and BCR were evaluated in a univariate and multivariable analysis. Overall and cancer-specific survival were also assessed.
RESULTS
We included 414 cases, 63.5% of them performed after radiotherapy. Before sRP the majority of patients had biopsy Gleason score (GS) ≤7 (55.5%) and imaging negative or with prostatic bed involvement only (93.3%). Final pathology showed aggressive histology in 39.7% (GS ≥9 27.6%), with 52.9% having ≥pT3 disease and 16% pN+. SM was positive in 29.7%. Five years BCR-Free, cancer-specific survival and OS were 56.7%, 97.7% and 92.1%, respectively. On multivariable analysis pathological T (pT3a odds ratio [OR] 2.939, 95% confidence interval [CI] 1.469-5.879; ≥pT3b OR 2.428-95% CI 1.333-4.423) and N stage (pN1 OR 2.871, 95% CI 1.503-5.897) were independent predictors of positive margins. Pathological T stage ≥T3b (OR 2.348 95% CI 1.338-4.117) and GS (up to OR 7.183, 95% CI 1.906-27.068 for GS >8) were independent predictors for BCR. Limitations include the retrospective nature of the study and limited follow-up.
CONCLUSIONS
In a contemporary series, sRP showed promising oncological control in the medium term despite aggressive pathological features. BCR risk increased in case of locally advanced disease and higher GS. Future studies are needed to confirm our findings.

Identifiants

pubmed: 33436329
pii: S1078-1439(20)30571-8
doi: 10.1016/j.urolonc.2020.11.002
pii:
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

296.e21-296.e29

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2020. Published by Elsevier Inc.

Auteurs

Giancarlo Marra (G)

Department of Urology, San Giovanni Battista Hospital, Città della Salute e della Scienza, University of Turin, Turin, Italy; Department of Urology, Institut Mutualiste Montsouris, Paris, France. Electronic address: drgiancarlomarra@gmail.com.

Robert Jeffrey Karnes (RJ)

Department of Urology, Mayo Clinic, Rochester, MN.

Giorgio Calleris (G)

Department of Urology, San Giovanni Battista Hospital, Città della Salute e della Scienza, University of Turin, Turin, Italy.

Marco Oderda (M)

Department of Urology, San Giovanni Battista Hospital, Città della Salute e della Scienza, University of Turin, Turin, Italy.

Paolo Alessio (P)

Department of Urology, San Giovanni Battista Hospital, Città della Salute e della Scienza, University of Turin, Turin, Italy.

Anna Palazzetti (A)

Department of Urology, San Giovanni Battista Hospital, Città della Salute e della Scienza, University of Turin, Turin, Italy.

Antonino Battaglia (A)

Department of Urology, San Giovanni Battista Hospital, Città della Salute e della Scienza, University of Turin, Turin, Italy; Department of Urology, Leuven University Hospitals, Leuven, Belgium.

Francesca Pisano (F)

Department of Urology, San Giovanni Battista Hospital, Città della Salute e della Scienza, University of Turin, Turin, Italy; Department of Urology, Fundaciò Puigvert, Barcelona, Spain.

Stefania Munegato (S)

Department of Urology, San Giovanni Battista Hospital, Città della Salute e della Scienza, University of Turin, Turin, Italy.

Fernando Munoz (F)

Department of Radiotherapy, Pasini Hospital, Aosta, Italy.

Claudia Filippini (C)

Department of Statistics, University of Turin, Turin, Italy.

Umberto Ricardi (U)

Department of Radiotherapy and School of Medicine Chair, University of Turin, Turin, Italy.

Estefania Linares (E)

Department of Urology, Institut Mutualiste Montsouris, Paris, France.

Rafael Sanchez-Salas (R)

Department of Urology, Institut Mutualiste Montsouris, Paris, France.

Sanchia Goonewardene (S)

Department of Urology, Urology Centre, Guy's Hospital, London, UK.

Prokar Dasgupta (P)

Department of Urology, Urology Centre, Guy's Hospital, London, UK.

Ben Challacombe (B)

Department of Urology, Urology Centre, Guy's Hospital, London, UK.

Rick Popert (R)

Department of Urology, Urology Centre, Guy's Hospital, London, UK.

Declan Cahill (D)

Department of Urology, Royal Marsden Hospital, London, UK.

David Gillatt (D)

Department of Urology, Bristol NHS Foundation Trust, Bristol, UK.

Raj Persad (R)

Department of Urology, Bristol NHS Foundation Trust, Bristol, UK.

Juan Palou (J)

Department of Urology, Fundaciò Puigvert, Barcelona, Spain.

Steven Joniau (S)

Department of Urology, Leuven University Hospitals, Leuven, Belgium.

Salvatore Smelzo (S)

Department of Urology, Clinique Saint Augustin, Bordeaux, France.

Thierry Piechaud (T)

Department of Urology, Clinique Saint Augustin, Bordeaux, France.

Alexandre De La Taille (A)

Department of Urology, CHU Mondor, Créteil, France.

Morgan Roupret (M)

Department of Urology, Pitié Salpétrière Hospital University Paris 6, Paris, France.

Simone Albisinni (S)

Department of Urology, Institut Jules Bordet, Université Libre de Bruxelles, Bruxelles, Belgium.

Roland van Velthoven (R)

Department of Urology, Institut Jules Bordet, Université Libre de Bruxelles, Bruxelles, Belgium.

Alessandro Morlacco (A)

Department of Urology, Mayo Clinic, Rochester, MN.

Sharma Vidit (S)

Department of Urology, Mayo Clinic, Rochester, MN.

Giorgio Gandaglia (G)

Department of Urology, OLV Hospital, Aalst, Belgium.

Alexander Mottrie (A)

Department of Urology, OLV Hospital, Aalst, Belgium.

Joseph Smith (J)

Department of Urology, Vanderbilt University, Medical Center North, Nashville, TN, USA.

Shreyas Joshi (S)

Department of Urology, Vanderbilt University, Medical Center North, Nashville, TN, USA.

Gabriel Fiscus (G)

Department of Urology, Vanderbilt University, Medical Center North, Nashville, TN, USA.

Andre Berger (A)

Department of Urology, USC Norris Comprehensive Cancer Center and Hospital, University of Southern California, CA.

Monish Aron (M)

Department of Urology, USC Norris Comprehensive Cancer Center and Hospital, University of Southern California, CA.

Andre Abreu (A)

Department of Urology, USC Norris Comprehensive Cancer Center and Hospital, University of Southern California, CA.

Inderbir S Gill (IS)

Department of Urology, USC Norris Comprehensive Cancer Center and Hospital, University of Southern California, CA.

Henk Van Der Poel (H)

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

Derya Tilki (D)

Department of Urology, Martini Klinik, Hamburg, Germany.

Declan Murphy (D)

Department of Urology, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.

Nathan Lawrentschuk (N)

Department of Urology, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.

John Davis (J)

Department of Urology, Division of Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX.

Paolo Gontero (P)

Department of Urology, San Giovanni Battista Hospital, Città della Salute e della Scienza, University of Turin, Turin, Italy.

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