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Prognostic value of premaintenance FDG PET/CT response in patients with newly diagnosed myeloma from the CASSIOPEIA trial

  • Françoise Kraeber-Bodéré*
  • , Bastien Jamet
  • , Sonja Zweegman
  • , Aurore Perrot
  • , Cyrille Hulin
  • , Denis Caillot
  • , Thierry Facon
  • , Xavier Leleu
  • , Karim Belhadj
  • , Emmanuel Itti
  • , Lionel Karlin
  • , Clément Bailly
  • , Mark-David Levin
  • , Monique C Minnema
  • , Caroline Bodet-Milin
  • , Bart de Keizer
  • , Jill Corre
  • , Pieter Sonneveld
  • , Philippe Moreau
  • , Thomas Carlier
  • Cyrille Touzeau
*Corresponding author for this work
  • Centre Hospitalier Universitaire de Nantes
  • Amsterdam UMC
  • Centre Hospitalier Universitaire de Toulouse
  • Bordeaux University Hospital CHU Bordeaux
  • Centre Hospitalier Universitaire Dijon
  • Université de Lille
  • Centre Hospitalier Universitaire de Poitiers
  • Aarhus University
  • Department of Nuclear Medicine
  • Centre Hospitalier Lyon-Sud Hématologie
  • Albert Schweitzer Hospital
  • University Medical Centre Utrecht
  • Laboratory of Hematology

Research output: Contribution to journalArticleAcademicpeer-review

2 Citations (Scopus)
2 Downloads (Pure)

Abstract

The CASSIOPEIA trial demonstrated superior progression-free survival (PFS) with the addition of daratumumab to bortezomib, thalidomide, and dexamethasone (D-VTd) induction/consolidation, and with daratumumab maintenance vs observation in transplant-eligible patients with newly diagnosed multiple myeloma (NDMM). The companion study, CASSIOPET, assessed the prognostic value of premaintenance (PM) positron emission tomography (PET)/computed tomography (CT) response, based on the standardized Deauville score on PFS and overall survival (OS), in addition to bone marrow (BM) minimal residual disease (MRD) detection by multiparameter flow cytometry (MFC) at 10-5 level. PM PET/CT was available for 225 patients: 112 patients treated with daratumumab after D-VTd (59) or bortezomib, thalidomide, and dexamethasone (VTd; 53), and 113 patients followed by observation after D-VTd (56) or VTd (57). At PM, 92% of the 175 baseline PET-positive patients achieved PET negativity, with a longer PFS in univariate analysis (P = .019) and a major trend of prolonged OS (P = .056). In univariate analysis, patients who achieved both PET and MFC negativity were found to have a better PFS (P < .0001) than those who had at least 1 positive result. In daratumumab-treated patients, PM PET negativity was associated with prolonged PFS and OS in univariate analysis (P = .0023 and P = .033, respectively), and double MFC and PET negativity was independently associated with PFS by multivariate analysis (P = .0006). This study confirms the prognostic relevance of a PM PET response in patients with NDMM treated with daratumumab in addition to MRD detection by MFC at the BM level. This trial was registered at ww.clinicaltrials.gov as #NCT02541383.

Original languageEnglish
Pages (from-to)3050-3058
Number of pages9
JournalBlood
Volume146
Issue number25
DOIs
Publication statusPublished - 18 Dec 2025

Bibliographical note

© 2025 American Society of Hematology. Published by Elsevier Inc. All rights are reserved, including those for text and data mining, AI training, and similar technologies.

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