Impact of minimal residual disease standardised assessment by FDG-PET/CT in transplant-eligible patients with newly diagnosed multiple myeloma enrolled in the imaging sub-study of the FORTE trial.

Complete metabolic response (CMR) FDG-PET/CT Minimal residual disease (MRD) Multiparameter flow cytometry (MFC) Newly diagnosed multiple myeloma (NDMM)

Journal

EClinicalMedicine
ISSN: 2589-5370
Titre abrégé: EClinicalMedicine
Pays: England
ID NLM: 101733727

Informations de publication

Date de publication:
Jun 2023
Historique:
received: 15 02 2023
revised: 03 05 2023
accepted: 08 05 2023
medline: 3 7 2023
pubmed: 3 7 2023
entrez: 3 7 2023
Statut: epublish

Résumé

18F-FDG-PET/CT is the current standard technique to define minimal residual disease (MRD) outside the bone marrow (BM) in multiple myeloma (MM), recently standardised applying the Deauville scores (DS) to focal lesions (FS) and bone marrow uptake (BMS) and defining the complete metabolic response (CMR) as uptake below the liver background (DS <4). In this analysis, we aimed at confirming the role of CMR, and complementarity with BM multiparameter flow cytometry (MFC) at 10 At B, 93% of patients had focal lesions within the bones (FS ≥4 in 89%) and 99% increased BM uptake (BMS ≥4 in 61%). At PM, CMR was achieved in 63% of patients, which was a strong predictor for prolonged PFS in univariate analysis at landmark time PM (HR 0.40, We herein confirm the applicability and validity of DS criteria to define CMR and its prognostic relevance and complementarity with MFC at the BM level. Amgen, Celgene/Bristol Myers Squibb, Italian Ministry of Health (RC-2022-2773423).

Sections du résumé

Background UNASSIGNED
18F-FDG-PET/CT is the current standard technique to define minimal residual disease (MRD) outside the bone marrow (BM) in multiple myeloma (MM), recently standardised applying the Deauville scores (DS) to focal lesions (FS) and bone marrow uptake (BMS) and defining the complete metabolic response (CMR) as uptake below the liver background (DS <4).
Methods UNASSIGNED
In this analysis, we aimed at confirming the role of CMR, and complementarity with BM multiparameter flow cytometry (MFC) at 10
Findings UNASSIGNED
At B, 93% of patients had focal lesions within the bones (FS ≥4 in 89%) and 99% increased BM uptake (BMS ≥4 in 61%). At PM, CMR was achieved in 63% of patients, which was a strong predictor for prolonged PFS in univariate analysis at landmark time PM (HR 0.40,
Interpretation UNASSIGNED
We herein confirm the applicability and validity of DS criteria to define CMR and its prognostic relevance and complementarity with MFC at the BM level.
Funding UNASSIGNED
Amgen, Celgene/Bristol Myers Squibb, Italian Ministry of Health (RC-2022-2773423).

Identifiants

pubmed: 37396807
doi: 10.1016/j.eclinm.2023.102017
pii: S2589-5370(23)00194-3
pmc: PMC10314158
doi:

Types de publication

Journal Article

Langues

eng

Pagination

102017

Informations de copyright

© 2023 The Author(s).

Déclaration de conflit d'intérêts

EZ receives honoraria from Janssen, Bristol-Myers Squibb, Amgen, Takeda. SO has received honoraria from Amgen, Celgene/Bristol Myers Squibb, and Janssen; has served on the advisory boards for Adaptive Biotechnologies, Janssen, Amgen, and Takeda. FG has received honoraria from Amgen, Celgene, Janssen, Takeda, Bristol Myers Squibb, AbbVie, and GlaxoSmithKline; has served on the advisory boards for Amgen, Celgene, Janssen, Takeda, Bristol Myers Squibb, AbbVie, GlaxoSmithKline, Roche, Adaptive Biotechnologies, Oncopeptides, bluebird bio, and Pfizer. MD has received honoraria for lectures from GlaxoSmithKline, Sanofi, and Janssen; has served on the advisory boards for GlaxoSmithKline, Sanofi, and Bristol Myers Squibb. AB has served on the advisory board for Amgen, Janssen, Takeda, Celgene, GlaxoSmithKline. MGa has received honoraria from Janssen, Bristol-Myers Squibb, Amgen, Takeda, GlaxoSmithKline. RZ has served on the advisory boards for Amgen, Celgene, Janssen, Takeda, Bristol Myers Squibb, GlaxoSmithKline, and Pfizer. BG has received honoraria from Amgen, Bristol Myers Squibb, Janssen, and Takeda; has served on the advisory boards for Amgen, Bristol Myers Squibb, GlaxoSmithKline, Janssen, Sanofi, and Takeda. AV received honoraria from Novartis, Advanced Accelerator Applications and GE Healthcare. FP receives honoraria and travel accommodation support from Celgene, Janssen, Takeda and has served on the advisory boards for Celgene BMS, Janssen, Amgen, GlaxoSmithKline. PT has received honoraria from Janssen, Celgene, Bristol Myers Squibb, Amgen, Takeda, AbbVie, Sanofi, GlaxoSmithKline, and Pfizer; has served on the data safety monitoring boards or advisory boards for Janssen, Celgene, Bristol Myers Squibb, and Amgen. KM has received honoraria from Celgene, Takeda, Amgen, Sanofi, Janssen. MB has received honoraria from Sanofi, Celgene, Amgen, Janssen, Novartis, Bristol Myers Squibb, and AbbVie; has served on the advisory boards for Janssen and GlaxoSmithKline; has received research funding from Sanofi, Celgene, Amgen, Janssen, Novartis, Bristol Myers Squibb, and Mundipharma. PM has received honoraria from and/or served on scientific boards for AbbVie, Alexion, Amgen, AstraZeneca, Astellas, BeiGene, Bristol-Myers Squibb/Celgene, Gilead, GlaxoSmithKline, Incyte, Janssen, Jazz, Novartis, Pfizer, Roche, Sanofi, and Takeda. MC has received honoraria from Janssen, Celgene, Amgen, Bristol Myers Squibb, GlaxoSmithKline, Takeda, AbbVie, Sanofi, Pfizer, and Adaptive Biotechnologies; has served on the advisory boards for Janssen, Bristol Myers Squibb, Sanofi, Amgen, GlaxoSmithKline, and Pfizer; has served on the speakers’ bureaus for Janssen, Celgene, and Sanofi. CN has been PET revisor for Keosys-Sanofi. The other authors declare no competing financial interests.

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Auteurs

Elena Zamagni (E)

IRCCS Azienda Ospedaliero-Universitaria di Bologna, Istituto di Ematologia "Seràgnoli", Bologna, Italy.
Dipartimento di Scienze Mediche e Chirurgiche, Università di Bologna, Bologna, Italy.

Stefania Oliva (S)

Division of Hematology, Azienda Ospedaliero-Universitaria Città della Salute e della Scienza di Torino, Torino, Italy.

Francesca Gay (F)

Division of Hematology, Azienda Ospedaliero-Universitaria Città della Salute e della Scienza di Torino, Torino, Italy.
Division of Hematology, Department of Molecular Biotechnology and Health Sciences, University of Torino, Torino, Italy.

Andrea Capra (A)

Division of Hematology, Department of Molecular Biotechnology and Health Sciences, University of Torino, Torino, Italy.

Delia Rota-Scalabrini (D)

Multidisciplinary Oncology Outpatient Clinic, Candiolo Cancer Institute, FPO-IRCCS, Torino, Italy.

Mattia D'Agostino (M)

Division of Hematology, Azienda Ospedaliero-Universitaria Città della Salute e della Scienza di Torino, Torino, Italy.
Division of Hematology, Department of Molecular Biotechnology and Health Sciences, University of Torino, Torino, Italy.

Angelo Belotti (A)

Department of Hematology, ASST Spedali Civili di Brescia, Brescia, Italy.

Monica Galli (M)

UO Hematology, ASST Papa Giovanni XXIII, Bergamo, Italy.

Manuela Racca (M)

Nuclear Medicine Unit, Candiolo Cancer Institute, FPO-IRCCS, Candiolo, Italy.

Renato Zambello (R)

Department of Medicine (DIMED), Hematology and Clinical Immunology, Padua University, Padua, Italy.

Barbara Gamberi (B)

Azienda USL - IRCCS di Reggio Emilia, Reggio Emilia, Italy.

Domenico Albano (D)

Nuclear Medicine Department, University of Brescia and ASST Spedali Civili Brescia, Brescia, Italy.

Luca Bertamini (L)

Division of Hematology, Azienda Ospedaliero-Universitaria Città della Salute e della Scienza di Torino, Torino, Italy.
Division of Hematology, Department of Molecular Biotechnology and Health Sciences, University of Torino, Torino, Italy.

Annibale Versari (A)

Nuclear Medicine Unit, Azienda Unità Sanitaria Locale-IRCCS di Reggio Emilia, Reggio Emilia, Italy.

Mariella Grasso (M)

Azienda Ospedaliera S. Croce-Carle, Cuneo, Italy.

Nicola Sgherza (N)

Hematology and Stem Cell Transplantation Unit, AOU Consorziale Policlinico, Bari, Italy.

Claudia Priola (C)

Division of Hematology, Department of Molecular Biotechnology and Health Sciences, University of Torino, Torino, Italy.

Francesca Fioritoni (F)

Ospedale Santo Spirito, Pescara, Italy.

Francesca Patriarca (F)

Hematologic Clinic and Transplant Center, University Hospital of Central Friuli, DAME, University of Udine, Udine, Italy.

Gabriella De Cicco (G)

IRCCS Azienda Ospedaliero-Universitaria di Bologna, Istituto di Ematologia "Seràgnoli", Bologna, Italy.
Dipartimento di Scienze Mediche e Chirurgiche, Università di Bologna, Bologna, Italy.

Tania Villanova (T)

Division of Hematology, Department of Molecular Biotechnology and Health Sciences, University of Torino, Torino, Italy.

Anna Pascarella (A)

UOC Ematologia, Ospedale dell'Angelo, Venezia Mestre, Italy.

Pietro Zucchetta (P)

Nuclear Medicine Unit, Department of Medicine DIMED, University-Hospital of Padova, Padova, Italy.

Paola Tacchetti (P)

IRCCS Azienda Ospedaliero-Universitaria di Bologna, Istituto di Ematologia "Seràgnoli", Bologna, Italy.

Stefano Fanti (S)

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

Katia Mancuso (K)

IRCCS Azienda Ospedaliero-Universitaria di Bologna, Istituto di Ematologia "Seràgnoli", Bologna, Italy.
Dipartimento di Scienze Mediche e Chirurgiche, Università di Bologna, Bologna, Italy.

Simona Barbato (S)

IRCCS Azienda Ospedaliero-Universitaria di Bologna, Istituto di Ematologia "Seràgnoli", Bologna, Italy.
Dipartimento di Scienze Mediche e Chirurgiche, Università di Bologna, Bologna, Italy.

Mario Boccadoro (M)

Division of Hematology, Department of Molecular Biotechnology and Health Sciences, University of Torino, Torino, Italy.

Pellegrino Musto (P)

Hematology and Stem Cell Transplantation Unit, AOU Consorziale Policlinico, Bari, Italy.
Department of Precision and Regenerative Medicine and Ionian Area, "Aldo Moro" University School of Medicine, Bari, Italy.

Michele Cavo (M)

IRCCS Azienda Ospedaliero-Universitaria di Bologna, Istituto di Ematologia "Seràgnoli", Bologna, Italy.
Dipartimento di Scienze Mediche e Chirurgiche, Università di Bologna, Bologna, Italy.

Cristina Nanni (C)

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

Classifications MeSH