Development and Validation of a Multi-institutional Nomogram of Outcomes for PSMA-PET-Based Salvage Radiotherapy for Recurrent Prostate Cancer.


Journal

JAMA network open
ISSN: 2574-3805
Titre abrégé: JAMA Netw Open
Pays: United States
ID NLM: 101729235

Informations de publication

Date de publication:
01 05 2023
Historique:
medline: 25 5 2023
pubmed: 23 5 2023
entrez: 23 5 2023
Statut: epublish

Résumé

Prostate-specific antigen membrane positron-emission tomography (PSMA-PET) is increasingly used to guide salvage radiotherapy (sRT) after radical prostatectomy for patients with recurrent or persistent prostate cancer. To develop and validate a nomogram for prediction of freedom from biochemical failure (FFBF) after PSMA-PET-based sRT. This retrospective cohort study included 1029 patients with prostate cancer treated between July 1, 2013, and June 30, 2020, at 11 centers from 5 countries. The initial database consisted of 1221 patients. All patients had a PSMA-PET scan prior to sRT. Data were analyzed in November 2022. Patients with a detectable post-radical prostatectomy prostate-specific antigen (PSA) level treated with sRT to the prostatic fossa with or without additional sRT to pelvic lymphatics or concurrent androgen deprivation therapy (ADT) were eligible. The FFBF rate was estimated, and a predictive nomogram was generated and validated. Biochemical relapse was defined as a PSA nadir of 0.2 ng/mL after sRT. In the nomogram creation and validation process, 1029 patients (median age at sRT, 70 years [IQR, 64-74 years]) were included and further divided into a training set (n = 708), internal validation set (n = 271), and external outlier validation set (n = 50). The median follow-up was 32 months (IQR, 21-45 months). Based on the PSMA-PET scan prior to sRT, 437 patients (42.5%) had local recurrences and 313 patients (30.4%) had nodal recurrences. Pelvic lymphatics were electively irradiated for 395 patients (38.4%). All patients received sRT to the prostatic fossa: 103 (10.0%) received a dose of less than 66 Gy, 551 (53.5%) received a dose of 66 to 70 Gy, and 375 (36.5%) received a dose of more than 70 Gy. Androgen deprivation therapy was given to 325 (31.6%) patients. On multivariable Cox proportional hazards regression analysis, pre-sRT PSA level (hazard ratio [HR], 1.80 [95% CI, 1.41-2.31]), International Society of Urological Pathology grade in surgery specimen (grade 5 vs 1+2: HR, 2.39 [95% CI, 1.63-3.50], pT stage (pT3b+pT4 vs pT2: HR, 1.91 [95% CI, 1.39-2.67]), surgical margins (R0 vs R1+R2+Rx: HR, 0.60 [95% CI, 0.48-0.78]), ADT use (HR, 0.49 [95% CI, 0.37-0.65]), sRT dose (>70 vs ≤66 Gy: HR, 0.44 [95% CI, 0.29-0.67]), and nodal recurrence detected on PSMA-PET scans (HR, 1.42 [95% CI, 1.09-1.85]) were associated with FFBF. The mean (SD) nomogram concordance index for FFBF was 0.72 (0.06) for the internal validation cohort and 0.67 (0.11) in the external outlier validation cohort. This cohort study of patients with prostate cancer presents an internally and externally validated nomogram that estimated individual patient outcomes after PSMA-PET-guided sRT.

Identifiants

pubmed: 37219907
pii: 2805173
doi: 10.1001/jamanetworkopen.2023.14748
pmc: PMC10208140
doi:

Substances chimiques

Prostate-Specific Antigen EC 3.4.21.77
Androgen Antagonists 0
Androgens 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2314748

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Auteurs

Constantinos Zamboglou (C)

Department of Radiation Oncology, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
German Cancer Consortium (DKTK), Partner Site Freiburg, Freiburg, Germany.
Berta-Ottenstein-Programme, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
German Oncology Center, University Hospital of the European University, Limassol, Cyprus.

Jan C Peeken (JC)

Department of Radiation Oncology, Klinikum rechts der Isar, Technical University of Munich (TUM), Munich, Germany.
Institute of Radiation Medicine (IRM), Department of Radiation Sciences (DRS), Helmholtz Zentrum, München, Germany.
Deutsches Konsortium für Translationale Krebsforschung (DKTK), Partner Site Munich, Munich, Germany.

Ali Janbain (A)

Cité University, AP-HP, European Hospital Georges-Pompidou, Clinical research unit, Clinical Investigation Center 1418 Clinical Epidemiology, INSERM, INRIA, HeKA, Paris, France.

Sandrine Katsahian (S)

Cité University, AP-HP, European Hospital Georges-Pompidou, Clinical research unit, Clinical Investigation Center 1418 Clinical Epidemiology, INSERM, INRIA, HeKA, Paris, France.

Iosif Strouthos (I)

Department of Radiation Oncology, German Oncology Center, University Hospital of the European University, Limassol, Cyprus.

Konstantinos Ferentinos (K)

Department of Radiation Oncology, German Oncology Center, University Hospital of the European University, Limassol, Cyprus.

Andrea Farolfi (A)

Division of Nuclear Medicine, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.

Stefan A Koerber (SA)

Department of Radiation Oncology, Heidelberg University Hospital, Heidelberg, Germany.
Clinical Cooperation Unit Radiation Oncology, German Cancer Research Center, Heidelberg, Germany.

Juergen Debus (J)

Department of Radiation Oncology, Heidelberg University Hospital, Heidelberg, Germany.
Clinical Cooperation Unit Radiation Oncology, German Cancer Research Center, Heidelberg, Germany.

Marco E Vogel (ME)

Department of Radiation Oncology, Klinikum rechts der Isar, Technical University of Munich (TUM), Munich, Germany.
Institute of Radiation Medicine (IRM), Department of Radiation Sciences (DRS), Helmholtz Zentrum, München, Germany.
Deutsches Konsortium für Translationale Krebsforschung (DKTK), Partner Site Munich, Munich, Germany.

Stephanie E Combs (SE)

Department of Radiation Oncology, Klinikum rechts der Isar, Technical University of Munich (TUM), Munich, Germany.
Institute of Radiation Medicine (IRM), Department of Radiation Sciences (DRS), Helmholtz Zentrum, München, Germany.
Deutsches Konsortium für Translationale Krebsforschung (DKTK), Partner Site Munich, Munich, Germany.

Alexis Vrachimis (A)

Department of Nuclear Medicine, German Oncology Center, University Hospital of the European University, Limassol, Cyprus.
C.A.R.I.C. Cancer Research & Innovation Center, Limassol, Cyprus.

Alessio Giuseppe Morganti (AG)

Division of Radiation Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.

Simon K B Spohn (SKB)

Department of Radiation Oncology, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
German Cancer Consortium (DKTK), Partner Site Freiburg, Freiburg, Germany.
Berta-Ottenstein-Programme, Faculty of Medicine, University of Freiburg, Freiburg, Germany.

Mohamed Shelan (M)

Department of Radiation Oncology, Inselspital Bern, University of Bern, Bern, Switzerland.

Daniel M Aebersold (DM)

Department of Radiation Oncology, Inselspital Bern, University of Bern, Bern, Switzerland.

Anca-Ligia Grosu (AL)

Department of Radiation Oncology, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
German Cancer Consortium (DKTK), Partner Site Freiburg, Freiburg, Germany.

Francesco Ceci (F)

Division of Nuclear Medicine, IEO European Institute of Oncology IRCCS, Milan, Italy.
Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy.

Christoph Henkenberens (C)

Department of Radiotherapy and Special Oncology, Medical School Hannover, Hannover, Germany.

Stephanie G C Kroeze (SGC)

Department of Radiation Oncology, University Hospital Zürich, University of Zurich, Zurich, Switzerland.
Department of Radiation Oncology KSA-KSB, Cantonal Hospital Aarau, Aarau, Switzerland.

Matthias Guckenberger (M)

Department of Radiation Oncology, University Hospital Zürich, University of Zurich, Zurich, Switzerland.

Stefano Fanti (S)

Division of Nuclear Medicine, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.

Claus Belka (C)

Department of Radiation Oncology, University Hospital, LMU Munich, Munich, Germany.

Peter Bartenstein (P)

Department of Nuclear Medicine, University Hospital, LMU Munich, Munich, Germany.

George Hruby (G)

Department of Radiation Oncology, Royal North Shore Hospital-University of Sydney, Sydney, Australia.

Sophia Scharl (S)

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

Thomas Wiegel (T)

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

Louise Emmett (L)

Department of Theranostics and Nuclear medicine, St Vincent's Hospital Sydney, Sydney, Australia.
St Vincent's Clinical School, University of New South Wales, Sydney, Australia.

Armelle Arnoux (A)

Cité University, AP-HP, European Hospital Georges-Pompidou, Clinical research unit, Clinical Investigation Center 1418 Clinical Epidemiology, INSERM, INRIA, HeKA, Paris, France.

Nina-Sophie Schmidt-Hegemann (NS)

Department of Radiation Oncology KSA-KSB, Cantonal Hospital Aarau, Aarau, Switzerland.

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