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Second Version of the Prostate Cancer Molecular Imaging Standardized Evaluation Framework Including Response Evaluation for Clinical Trials (PROMISE V2)

  • Robert Seifert
  • , Louise Emmett
  • , Steven P. Rowe
  • , Ken Herrmann
  • , Boris Hadaschik
  • , Jeremie Calais
  • , Frederik L. Giesel
  • , Robert Reiter
  • , Tobias Maurer
  • , Matthias Heck
  • , Andrei Gafita
  • , Michael J. Morris
  • , Stefano Fanti
  • , Wolfgang A. Weber
  • , Thomas A. Hope
  • , Michael S. Hofman
  • , Wolfgang Peter Fendler
  • , Matthias Eiber
  • University Hospital of Essen
  • St. Vincent's Hospital Sydney
  • Johns Hopkins School of Medicine
  • David Geffen School of Medicine at UCLA
  • Medical Faculty and University Hospital Düsseldorf
  • University Medical Center Hamburg-Eppendorf
  • Technische Universität München
  • Bavarian Cancer Research Center (BZKF)
  • Weill Cornell Medical College
  • IRCCS AOU di Bologna
  • University of California San Francisco
  • Peter Maccallum Cancer Centre
  • University of Melbourne
  • PET Committee of the German Society of Nuclear Medicine

Publikation: Beitrag in FachzeitschriftÜbersichtsartikelBegutachtung

220 Zitate (Scopus)

Abstract

Context: Prostate-specific membrane antigen (PSMA) targeting positron emission tomography (PET) is emerging to become a reference imaging tool for the staging and restaging of patients with prostate cancer for both clinical routine and trials. The prostate cancer molecular imaging standardized evaluation (PROMISE) criteria have been proposed as a framework for whole-body staging (molecular imaging TNM staging, denoted miTNM staging) to describe the prostate cancer disease extent on PSMA-PET. Objective: To create a comprehensive and integrated framework for PSMA-PET image interpretation and reporting. Evidence acquisition: We propose the PROMISE V2 framework, which integrates an updated miTNM system, improved assessment of local disease, and a slightly modified PSMA-expression score for clinical routine. We have added a response monitoring framework defining qualitative and quantitative parameters to be recorded for a longitudinal assessment in clinical trials. Evidence synthesis: We provide a comprehensive literature review on the current use of the PROMISE framework in clinical research and prospective trials. PROMISE variables demonstrate a clear association with survival. PSMA expression assessed by the PSMA-expression score was used in several trials, and a low PSMA-expression score is a negative prognosticator of overall survival after 177Lu-PSMA radioligand therapy. The proposed imaging parameters recorded for response assessment in clinical trials can be utilized to determine response according to PSMA-PET progression (PPP) or Response Evaluation Criteria in PSMA-PET/Computed Tomography (RECIP) frameworks, but also future response criteria. Conclusions: PROMISE V2 offers standardized reporting of disease extent for clinical routine and research. Parameters recorded within clinical trials facilitate objective response assessment. Patient summary: Prostate-specific membrane antigen (PSMA) targeting positron emission tomography (PET) has become a standard imaging examination for prostate cancer. We propose a comprehensive framework for the analysis and reporting of PSMA-PET findings that will improve the communication between imaging experts and uro-oncologists.

OriginalspracheEnglisch
Seiten (von - bis)405-412
Seitenumfang8
FachzeitschriftEuropean Urology
Jahrgang83
Ausgabenummer5
DOIs
PublikationsstatusVeröffentlicht - Mai 2023

UN SDGs

Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung

  1. SDG 3 – Gute Gesundheit und Wohlergehen
    SDG 3 – Gute Gesundheit und Wohlergehen

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