Efficacy of Intravenous Immunoglobulin for Preventing Infections in Patients with Multiple Myeloma.


Journal

Clinical lymphoma, myeloma & leukemia
ISSN: 2152-2669
Titre abrégé: Clin Lymphoma Myeloma Leuk
Pays: United States
ID NLM: 101525386

Informations de publication

Date de publication:
05 2021
Historique:
received: 20 10 2020
revised: 02 12 2020
accepted: 21 12 2020
pubmed: 16 3 2021
medline: 29 1 2022
entrez: 15 3 2021
Statut: ppublish

Résumé

Despite many recent advances in the treatment of multiple myeloma (MM), infection remains a major cause of morbidity and mortality. Prior studies have shown mixed results using intravenous immunoglobulin (IVIG) to prevent infections in MM and were conducted prior to most modern MM therapies. We retrospectively reviewed all patients with MM treated with IVIG at our institution from 2010 to 2017. The primary endpoint was the incidence rate ratio (IRR) of infectious events (IEs) per patient-year during IVIG versus observation. A total of 68 patients were included; 151 IEs occurred during 918 months of IVIG treatment, whereas 446 IEs occurred during 2484 months of observation. Although the annual rate of IEs was substantially higher during periods of progressive disease (PD) compared with non-PD (4.9 vs. 1.8; P < .001), most IEs occurred during periods of non-PD (75% vs. 25% during PD). There was no overall difference in the annual rate of IEs per patient between IVIG and observation (1.97 vs. 2.16; IRR, 0.92; 95% confidence interval [CI], 0.76-1.10; P = .376). The subgroup of patients with hypogammaglobulinemia and whose myeloma was in a non-PD phase had a significant reduction in all-grade IEs (1.20 vs. 1.92; IRR, 0.63; 95% CI, 0.45-0.88; P = .009) and ≥ grade 3 IEs (0.25 vs. 0.56; IRR, 0.45; 95% CI, 0.22-0.94; P = .041) with IVIG compared with observation. Although treatment with IVIG did not show benefit in the overall population, there may be subgroups of patients that derive significant benefit. Additional observational studies are needed to confirm these findings and further refine patient selection.

Identifiants

pubmed: 33716054
pii: S2152-2650(21)00053-7
doi: 10.1016/j.clml.2020.12.026
pii:
doi:

Substances chimiques

Immunoglobulins, Intravenous 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e470-e476

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Auteurs

Guido Lancman (G)

Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.

Katleen Lozada (K)

Icahn School of Medicine at Mount Sinai, New York, NY.

Nida Athar (N)

Icahn School of Medicine at Mount Sinai, New York, NY.

Samantha Jacobs (S)

Division of Infectious Diseases, Icahn School of Medicine at Mount Sinai, New York, NY.

John Doucette (J)

Biostatistics, Department of Environmental Medicine and Public Health, Icahn School of Medicine at Mount Sinai, New York, NY.

Hearn Jay Cho (HJ)

Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.

Sundar Jagannath (S)

Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.

Deepu Madduri (D)

Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.

Samir Parekh (S)

Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.

Shambavi Richard (S)

Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.

Joshua Richter (J)

Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.

Ajai Chari (A)

Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY. Electronic address: ajai.chari@mountsinai.org.

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Classifications MeSH