Salvage radiotherapy is effective in patients with PSMA-PET-negative biochemical recurrence- results of a retrospective study.


Journal

Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology
ISSN: 1879-0887
Titre abrégé: Radiother Oncol
Pays: Ireland
ID NLM: 8407192

Informations de publication

Date de publication:
07 2023
Historique:
received: 21 11 2022
revised: 12 04 2023
accepted: 17 04 2023
medline: 21 6 2023
pubmed: 6 5 2023
entrez: 5 5 2023
Statut: ppublish

Résumé

The present study aimed to assess whether SRT to the prostatic fossa should be initiated in a timely manner after detecting biochemical recurrence (BR) in patients with prostate cancer, when no correlate was identified with prostate-specific membrane antigen positron emission tomography (PSMA-PET). This retrospective, multicenter analysis included 1222 patients referred for PSMA-PET after a radical prostatectomy due to BR. Exclusion criteria were: pathological lymph node metastases, prostate-specific antigen (PSA) persistence, distant or lymph node metastases, nodal irradiation, and androgen deprivation therapy (ADT). This led to a cohort of 341 patients. Biochemical progression-free survival (BPFS) was the primary study endpoint. The median follow-up was 28.0 months. The 3-year BPFS was 71.6% in PET-negative cases and 80.8% in locally PET-positive cases. This difference was significant in univariate (p = 0.019), but not multivariate analyses (p = 0.366, HR: 1.46, 95%CI: 0.64-3.32). The 3-year BPFS in PET-negative cases was significantly influenced by age (p = 0.005), initial pT3/4 (p < 0.001), pathology scores (ISUP) ≥ 3 (p = 0.026), and doses to fossa > 70 Gy (p = 0.027) in univariate analyses. In multivariate analyses, only age (HR: 1.096, 95%CI: 1.023-1.175, p = 0.009) and PSA-doubling time (HR: 0.339, 95%CI: 0.139-0.826, p = 0.017) remained significant. To our best knowledge, this study provided the largest SRT analysis in patients without ADT that were lymph node-negative on PSMA-PET. A multivariate analysis showed no significant difference in BPFS between locally PET-positive and PET-negative cases. These results supported the current EAU recommendation to initiate SRT in a timely manner after detecting BR in PET negative patients.

Sections du résumé

BACKGROUND/PURPOSE
The present study aimed to assess whether SRT to the prostatic fossa should be initiated in a timely manner after detecting biochemical recurrence (BR) in patients with prostate cancer, when no correlate was identified with prostate-specific membrane antigen positron emission tomography (PSMA-PET).
MATERIALS AND METHODS
This retrospective, multicenter analysis included 1222 patients referred for PSMA-PET after a radical prostatectomy due to BR. Exclusion criteria were: pathological lymph node metastases, prostate-specific antigen (PSA) persistence, distant or lymph node metastases, nodal irradiation, and androgen deprivation therapy (ADT). This led to a cohort of 341 patients. Biochemical progression-free survival (BPFS) was the primary study endpoint.
RESULTS
The median follow-up was 28.0 months. The 3-year BPFS was 71.6% in PET-negative cases and 80.8% in locally PET-positive cases. This difference was significant in univariate (p = 0.019), but not multivariate analyses (p = 0.366, HR: 1.46, 95%CI: 0.64-3.32). The 3-year BPFS in PET-negative cases was significantly influenced by age (p = 0.005), initial pT3/4 (p < 0.001), pathology scores (ISUP) ≥ 3 (p = 0.026), and doses to fossa > 70 Gy (p = 0.027) in univariate analyses. In multivariate analyses, only age (HR: 1.096, 95%CI: 1.023-1.175, p = 0.009) and PSA-doubling time (HR: 0.339, 95%CI: 0.139-0.826, p = 0.017) remained significant.
CONCLUSION
To our best knowledge, this study provided the largest SRT analysis in patients without ADT that were lymph node-negative on PSMA-PET. A multivariate analysis showed no significant difference in BPFS between locally PET-positive and PET-negative cases. These results supported the current EAU recommendation to initiate SRT in a timely manner after detecting BR in PET negative patients.

Identifiants

pubmed: 37146766
pii: S0167-8140(23)00216-5
doi: 10.1016/j.radonc.2023.109678
pii:
doi:

Substances chimiques

Prostate-Specific Antigen EC 3.4.21.77
Androgen Antagonists 0
Gallium Radioisotopes 0

Types de publication

Multicenter Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

109678

Informations de copyright

Copyright © 2023 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Sophia Scharl (S)

Department of Radiation Oncology, University Hospital Ulm, Germany. Electronic address: Sophia.scharl@uniklinik-ulm.de.

Constantinos Zamboglou (C)

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

Iosif Strouthos (I)

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.

Francesca Serani (F)

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

Helena Lanzafame (H)

Division of Nuclear Medicine, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy; Department of Radiation Oncology, Royal North Shore Hospital - University of Sydney, Australia.

Alessio Giuseppe Morganti (A)

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

Christian Trapp (C)

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

Stefan A Koerber (SA)

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

Jürgen Debus (J)

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

Jan C Peeken (JC)

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

Marco M E Vogel (MME)

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

Simon K B Spohn (SKB)

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

Juri Ruf (J)

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

Anca-Ligia Grosu (AL)

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

Francesco Ceci (F)

Division of Nuclear Medicine, IEO European Institute of Oncology IRCCS, Milan, Italy.

Wolfgang P Fendler (WP)

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

Peter Bartenstein (P)

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

Stephanie G C Kroeze (SGC)

Department of Radiation Oncology, University Hospital Ulm, Germany; Radiation Oncology Center KSA-KSB, Canton Hospital of Aarau, Aarau, Switzerland.

Matthias Guckenberger (M)

Department of Radiation Oncology, University Hospital Ulm, Germany.

Manuel Krafcsik (M)

Department of Radiation Oncology, University Hospital Ulm, Germany.

Christina Klopscheck (C)

University Hospital Ulm, Ulm, Germany.

Stefano Fanti (S)

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

George Hruby (G)

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

Louise Emmett (L)

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

Claus Belka (C)

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

Christian Stief (C)

Department of Urology, University Hospital, LMU Munich, Germany.

Nina-Sophie Schmidt-Hegemann (NS)

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

Christoph Henkenberens (C)

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

Benjamin Mayer (B)

Institute for Epidemiology and Medical Biometry, University Ulm, Ulm, Germany.

Jonathan Miksch (J)

Department of Nuclear Medicine, University Hospital Ulm, University Ulm, Ulm, Germany.

Mohamed Shelan (M)

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

Daniel M Aebersold (DM)

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

Reinhard Thamm (R)

Department of Radiation Oncology, University Hospital Ulm, Germany.

Thomas Wiegel (T)

Department of Radiation Oncology, University Hospital Ulm, Germany.

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