Indications for and complications of pelvic lymph node dissection in prostate cancer: accuracy of available nomograms for the prediction of lymph node invasion.


Journal

BJU international
ISSN: 1464-410X
Titre abrégé: BJU Int
Pays: England
ID NLM: 100886721

Informations de publication

Date de publication:
03 2021
Historique:
pubmed: 2 9 2020
medline: 21 9 2021
entrez: 2 9 2020
Statut: ppublish

Résumé

To externally validate the currently available nomograms for predicting lymph node invasion (LNI) in patients with prostate cancer (PCa) and to assess the potential risk of complications of extended pelvic lymph node dissection (ePLND) when using the recommended threshold. A total of 14 921 patients, who underwent radical prostatectomy with ePLND at eight European tertiary referral centres, were retrospectively identified. After exclusion of patients with incomplete biopsy or pathological data, 12 009 were included. Of these, 609 had undergone multiparametic magnetic resonance imaging-targeted biopsies. Among ePLND-related complications we included lymphocele, lymphoedema, haemorrhage, infection and sepsis. The performances of the Memorial Sloan Kettering Cancer Centre (MSKCC), Briganti 2012, Briganti 2017, Briganti 2019, Partin 2016 and Yale models were evaluated using receiver-operating characteristic curve analysis (area under the curve [AUC]), calibration plots, and decision-curve analysis. Overall, 1158 patients (9.6%) had LNI, with a mean of 17.7 and 3.2 resected and positive nodes, respectively. No significant differences in AUCs were observed between the MSKCC (0.79), Briganti 2012 (0.79), Partin 2016 (0.78), Yale (0.80), Briganti 2017 (0.81) and Briganti 2019 (0.76) models. A direct comparison of older models showed that better discrimination was achieved with the MSKCC and Briganti 2012 nomograms. A tendency for underestimation was seen for all the older models, whereas the Briganti 2017 and 2019 nomograms tended to overestimate LNI risk. Decision-curve analysis showed a net benefit for all models, with a lower net benefit for the Partin 2016 and Briganti 2019 models. ePLND-related complications were experienced by 1027 patients (8.9%), and 12.6% of patients with pN1 disease. The currently available nomograms have similar performances and limitations in the prediction of LNI. Miscalibration was present, however, for all nomograms showing a net benefit. In patients with only systematic biopsy, the MSKCC and Briganti 2012 nomograms were superior in the prediction of LNI.

Identifiants

pubmed: 32869940
doi: 10.1111/bju.15220
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Validation Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

318-325

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© 2020 The Authors BJU International © 2020 BJU International Published by John Wiley & Sons Ltd.

Références

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Auteurs

Marco Oderda (M)

Division of Urology, Città della Salute e della Scienza, Molinette Hospital, University of Turin, Torino, Italy.

Romain Diamand (R)

Urology Department, Hôpital Erasme, University Clinics of Brussels, Université Libre de Bruxelles, Brussels, Belgium.

Simone Albisinni (S)

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

Giorgio Calleris (G)

Division of Urology, Città della Salute e della Scienza, Molinette Hospital, University of Turin, Torino, Italy.

Antonio Carbone (A)

Urology Unit, Department of Medico-Surgical Sciences and Biotechnologies, Sapienza University of Rome, Latina, Italy.

Marco Falcone (M)

Division of Urology, Città della Salute e della Scienza, Molinette Hospital, University of Turin, Torino, Italy.

Gaelle Fiard (G)

Urology Department, CHU de Grenoble, Grenoble, France.

Giorgio Gandaglia (G)

Unit of Urology/Department of Oncology, URI, IRCCS San Raffaele Hospital, Milan, Italy.

Alessandro Marquis (A)

Division of Urology, Città della Salute e della Scienza, Molinette Hospital, University of Turin, Torino, Italy.

Giancarlo Marra (G)

Division of Urology, Città della Salute e della Scienza, Molinette Hospital, University of Turin, Torino, Italy.
Department of Urology, Institut Mutualiste Montsouris, Université Paris Descartes, Paris, France.

Cinzia Parola (C)

Division of Urology, Città della Salute e della Scienza, Molinette Hospital, University of Turin, Torino, Italy.

Antonio Pastore (A)

Urology Unit, Department of Medico-Surgical Sciences and Biotechnologies, Sapienza University of Rome, Latina, Italy.

Alexandre Peltier (A)

Urology Department, Hôpital Erasme, University Clinics of Brussels, Université Libre de Bruxelles, Brussels, Belgium.

Guillaume Ploussard (G)

Quint Fonsegrives and Institut Universitaire du Cancer, La Croix du Sud Hospital, Toulouse, France.

Thierry Roumeguère (T)

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

Rafael Sanchez-Salas (R)

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

Giuseppe Simone (G)

Urology Department, Regina Elena National Cancer Institute, Rome, Italy.

Salvatore Smelzo (S)

Urology Unit, San Raffaele Turro, Milan, Italy.

John H Witt (JH)

Department of Urology, St Antonius Hospital Gronau, Gronau, Germany.

Paolo Gontero (P)

Division of Urology, Città della Salute e della Scienza, Molinette Hospital, University of Turin, Torino, Italy.

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