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  5. Positron emission tomography with computed tomography (PET/CT) and minimal residual disease (MRD) for efficacy assessment in transplant-ineligible newly diagnosed myeloma (Ti NDMM) patients (pts): IMROZ analysis.

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Article
en
2025

Positron emission tomography with computed tomography (PET/CT) and minimal residual disease (MRD) for efficacy assessment in transplant-ineligible newly diagnosed myeloma (Ti NDMM) patients (pts): IMROZ analysis.

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en
2025
Vol 43 (16_suppl)
Vol. 43
DOI: 10.1200/jco.2025.43.16_suppl.7551

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Meletios A Dimopoulos
Meletios A Dimopoulos

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Elena Zamagni
Thierry Façon
Meletios A Dimopoulos
+17 more

Abstract

7551 Background: MRD is a measure of response in the bone marrow (BM) but is limited by patchy infiltration of BM plasma cells and lack of plasmacytoma assessment. Imaging-based MRD assessment, which is non-invasive, such as PET/CT, may overcome these limitations, and distinguish metabolically active MM from non-active. Isatuximab (Isa) is an anti-CD38 monoclonal antibody approved in combination with bortezomib, lenalidomide and dexamethasone (VRd) in Ti NDMM pts based on the Phase 3 IMROZ study. Here, we present an analysis of IMROZ (NCT03319667), investigating PET/CT negativity (−) with MRD− in front line efficacy assessment. Methods: In IMROZ, pts were randomized 3:2 to receive Isa-VRd or VRd as initiation, then Isa-Rd or Rd as maintenance. BM MRD was assessed by next generation sequencing at 10 -5 sensitivity at baseline (BL), then in case of complete response (CR) or very good partial response at end of initiation, and every 6 months for 2 years, then once a year until disease progression (PD). PET/CT scans were assessed by central review and performed at BL, then yearly until PD; if positive for soft tissue plasmacytoma, repeated at time of CR and/or end of induction, then following time points for MRD assessment. PET/CT positivity (+) was defined as FDG 5PS Score ≥4, and PET/CT− as FDG 5PS ≤3. Results: Across the global and China populations, 244 Isa-VRd and 162 VRd pts had PET/CT at BL, of which 153 (62.7%) and 101 (62.3%) were PET/CT+, respectively. Of these, 121 (41.6%) and 83 (43.0%) had a post-BL PET/CT assessment. 155 pts presented with plasmacytoma at BL (95 Isa-VRd, 60 VRd), with comparable BL characteristics to the global population. Among PET+ pts at BL, the double negativity rate (PET/CT FDG 5PS score ≤3 + MRD−) was significantly higher in Isa-VRd pts than VRd (odds ratio [OR] 1.54; 95% CI 1.04-2.29; p=0.0155), and similarly for double negativity + ≥CR (OR 1.60; 95% CI 1.07-2.38; p=0.0108). As shown in Table, more Isa-VRd than VRd pts with plasmacytoma reached PET/CT 5PS ≤3 and MRD−, and PET/CT 5PS ≤3 with MRD− + ≥CR. Progression-free survival (PFS) in pts PET/CT+ at BL was in favor of the Isa-VRd arm (median PFS [mPFS] not reached [NR; 95% CI 59.4-NR]) vs VRd (mPFS 49.1 [95% CI 39.1 -NR]) (hazard ratio [HR] 0.58; 95% CI 0.39-0.88; p=0.6303), and HR was comparable to the intent to treat population. PFS in pts with plasmacytoma at BL was similar to the global population (HR 0.685; 95% CI 0.40-1.18; p=0.5332). Conclusions: This analysis of IMROZ shows the prognostic value of BL PET/CT findings. More Isa-VRd pts reached double negativity than VRd, including pts with plasmacytomas. This translated to a better PFS in pts treated with Isa-VRd. Clinical trial information: NCT03319667 . Isa-VRd (n=77) VRd (n=52) PET/CT 5PS score ≤3 and MRD−, % 45.5 34.6 OR (95% CI), p 1.57 (0.76-3.26), 0.1107 PET/CT 5PS score ≤3 and MRD− + ≥CR, % 44.2 32.7 OR (95% CI), p 1.63 (0.78-3.39), 0.0966

How to cite this publication

Elena Zamagni, Thierry Façon, Meletios A Dimopoulos, Xavier P. Leleu, Meral Beksaç, Luděk Pour, Roman Hájek, Zhuogang Liu, Jiří Minařík, Philippe Moreau, Joanna Romejko‐Jarosińska, Ivan Spicka, Tom Martin, Lugui Qiu, Christos Sachpekidis, Ercem Kodas, Helgi van de Velde, Liang Zhao, Robert Orlowski, Hartmut Goldschmidt (2025). Positron emission tomography with computed tomography (PET/CT) and minimal residual disease (MRD) for efficacy assessment in transplant-ineligible newly diagnosed myeloma (Ti NDMM) patients (pts): IMROZ analysis.. , 43(16_suppl), DOI: https://doi.org/10.1200/jco.2025.43.16_suppl.7551.

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Publication Details

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Article

Year

2025

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Language

en

DOI

https://doi.org/10.1200/jco.2025.43.16_suppl.7551

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