Characteristics and incidence of infections in patients with multiple myeloma treated by bispecific antibodies: a national retrospective study on the behalf of G2I and IFM.

Adverse event Bispecific antibodies Epidemiology Infections Multicentric Multiple myeloma Retrospective

Journal

Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases
ISSN: 1469-0691
Titre abrégé: Clin Microbiol Infect
Pays: England
ID NLM: 9516420

Informations de publication

Date de publication:
01 Mar 2024
Historique:
received: 21 11 2023
revised: 10 02 2024
accepted: 27 02 2024
medline: 4 3 2024
pubmed: 4 3 2024
entrez: 3 3 2024
Statut: aheadofprint

Résumé

Bispecific antibodies (BsAbs) are an effective treatment used in relapsed/refractory multiple myeloma. Despite a well-tolerated safety profile, infectious events appeared to be frequent in clinical trials. Real-world data on epidemiology, characteristics, risk factors and outcomes of infections in patients treated with BsAb are still needed. A retrospective, multicenter study in BsAb-treated MM patients was conducted in 14 French centers from December 2020 to February 2023. The primary objective was to describe the incidence of infections that required hospitalization, specific treatment, or adaptation in BsAb administration. Among 229 MM patients treated with BsAb, 153 (67%) received teclistamab, 47 (20%) received elranatamab and 29 (13%) talquetamab. We reported a total of 234 infections, including 123 (53%) of grade ≥3. Predominant infections affected the respiratory tract (n=116, 50%) followed by bacteremias (n=36, 15%). Hospitalization rate was 56% (n=131), and 20 (9%) infections resulted in death. Global cumulative incidence of first infection was 70% in all patients, 73% in patients treated with BCMA-targeting and 51% with GPRC5D-targeting BsAb. In univariate analyses, corticosteroids for CRS/ICANS were associated with a higher risk of first infection (HR=2.13; 95CI:1.38-3.28), while GPRC5D-targeting BsAb and antibacterial prophylaxis were associated with lower risk (HR=0.53; 95CI:0.3-0.94 and HR=0.65; 95CI:0.46-0.9). Fine and Gray multivariate model found that only corticosteroids for CRS/ICANS were correlated with a higher risk of first infection (HR=2.01; 95CI:1.27-3.19). The implementation of preventive measures that aim to mitigate the risk of infection under BsAb is pivotal, notably in patients who received corticosteroids for CRS/ICANS.

Identifiants

pubmed: 38432433
pii: S1198-743X(24)00098-3
doi: 10.1016/j.cmi.2024.02.023
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Ltd.

Auteurs

Aurélie Jourdes (A)

Service de maladies infectieuses et tropicales, Centre Hospitalo-universitaire (CHU) de Toulouse, France.

Elise Cellerin (E)

Service d'hématologie, Centre Hospitalo-universitaire (CHU) de Tours, France.

Cyrille Touzeau (C)

Service d'hématologie, Centre Hospitalo-universitaire (CHU) Hôtel Dieu, Nantes, France.

Stéphanie Harel (S)

Service d'immuno-hématologie, Hôpital St-Louis, AP-HP, Paris, France.

Blandine Denis (B)

Service de maladies infectieuses et tropicales, Hôpital St-Louis, AP-HP, Paris, France.

Guillaume Escure (G)

Service d'hématologie, Centre Hospitalo-universitaire (CHU) de Lille, France.

Emmanuel Faure (E)

Service d'hématologie, Centre Hospitalo-universitaire (CHU) de Lille, France; U1019-UMR 9017-Centre d'Infection et d'Immunité de Lille, INSERM, Centre National de la Recherche Scientifique, Institut Pasteur de Lille, Université de Lille, Lille, France.

Simon Jamard (S)

Service de Médecine infectieuse et tropicale, Centre Hospitalo-Universitaire (CHU) de Tours, France.

Francois Danion (F)

Service de maladies infectieuses et tropicales, Les Hôpitaux Universitaires de Strasbourg, Strasbourg, Grand Est, France; Laboratoire d'Immuno-rhumatologie moléculaire UMR_S 1109, INSERM, Strasbourg, Grand Est, France.

Cécile Sonntag (C)

Service d'hématologie, Institut de Cancérologie de Strasbourg Europe (ICANS), Strasbourg, France.

Florence Ader (F)

Département des Maladies infectieuses et tropicales, Hospices Civils de Lyon, F-69004,Lyon, France; Centre International de Recherche en Infectiologie (CIRI), Inserm 1111, Université Claude Bernard Lyon 1, CNRS, UMR5308, École Normale Supérieure de Lyon, Univ Lyon, F-69007, Lyon, France.

Lionel Karlin (L)

Service d'hématologie, Centre Hospitalier Lyon-Sud, Lyon, France.

Sarah Soueges (S)

Département des Maladies infectieuses et tropicales, Hospices Civils de Lyon, F-69004,Lyon, France.

Clarisse Cazelles (C)

Service d'hématologie, Hôpital Necker-Enfants Malades, AP-HP, Paris, France; Institut Cochin, Université de Paris, CNRS UMR8104, INSERM U1016, Paris, France.

Clémentine de La Porte des Vaux (C)

Service de maladies infectieuses et tropicales, Hôpital Necker-Enfants Malades, AP-HP, Paris, France.

Laurent Frenzel (L)

Service d'hématologie, Hôpital Necker-Enfants Malades, AP-HP, Paris, France; CEREMAST, Institut Imagine, INSERM U1163, AP-HP, Hôpital Necker-Enfants Malades, Université Paris Centre, Paris, France.

Fanny Lanternier (F)

Service de maladies infectieuses et tropicales, Hôpital Necker-Enfants Malades, AP-HP, Paris, France; Institut Pasteur, Université Paris Cité, Centre National de Référence Mycoses Invasives et Antifongiques, Groupe de Recherche Translationnelle en Mycologie, Département de Mycologie, Paris, Île-de-France, France.

Xavier Brousse (X)

Service de maladies infectieuses et tropicales, Centre Hospitalo-universitaire (CHU) de Bordeaux, France.

Titouan Cazaubiel (T)

Service d'hématologie, Centre Hospitalo-universitaire (CHU) de Bordeaux, France; Equipe génomique et immunologie du myélome multiple, Centre de Recherche en Cancérologie de Toulouse INSERM U1037, Université Paul Sabatier, Toulouse, France.

Pierre Berger (P)

Infectiologie Transversale, Institut Paoli-Calmettes, Marseille, France.

Aude Collignon (A)

Service d'hématologie, Institut Paoli-Calmettes, Marseille, France.

Mathieu Blot (M)

Service de maladies infectieuses et tropicales, Centre Hospitalo-universitaire (CHU) de Dijon-Bourgogne, France; INSERM, Université de Bourgogne, CIC 1432, Module Épidémiologie Clinique, Dijon, France; Equipe Lipness, INSERM LNC-UMR1231 et LabEx LipSTIC, Université de Burgundy, Dijon, France.

Andrea Pieragostini (A)

Service d'hématologie, Centre Hospitalo-universitaire (CHU) de Dijon-Bourgogne, France.

Morgane Charles (M)

Service de maladies infectieuses et tropicales, Centre Hospitalo-universitaire (CHU) d'Estaing, Clermont-Ferrand, France.

Carine Chaleteix (C)

Service d'hématologie, Centre Hospitalo-universitaire (CHU) d'Estaing, Clermont-Ferrand, France.

Alexis Redor (A)

Service de maladies infectieuses et tropicales, Centre Hospitalier de Perpignan, France.

Virginie Roland (V)

Service d'hématologie, Centre Hospitalier de Perpignan, France.

Tom Cartau (T)

Service de maladies infectieuses et tropicales, Centre Hospitalo-universitaire (CHU) Côte de Nacre, Caen, France.

Margaret Macro (M)

Service d'hématologie, Institut bas Normand d'Hématologie, CHU Caen Normandie, Caen, France.

Thomas Chalopin (T)

Service d'hématologie, Centre Hospitalo-universitaire (CHU) de Tours, France.

Nicolas Vallet (N)

Service d'hématologie, Centre Hospitalo-universitaire (CHU) de Tours, France; Equipe INSERM U1069 N2COx, groupe LNOx, Université de Tours, France.

Aurore Perrot (A)

Service de maladies infectieuses et tropicales, Centre Hospitalo-universitaire (CHU) de Bordeaux, France; Service d'hématologie, Centre Hospitalo-universitaire (CHU) de Toulouse, Institut Universitaire du Cancer de Toulouse-Oncopole (IUCT-O), Toulouse, France.

Guillaume Martin-Blondel (G)

Service de maladies infectieuses et tropicales, Centre Hospitalo-universitaire (CHU) de Toulouse, France; Institut Toulousain des Maladies Infectieuses et Inflammatoires (Infinity) INSERM, Université Toulouse III, Toulouse, France. Electronic address: martin-blondel.g@chu-toulouse.fr.

Classifications MeSH