Endothelial injury and dysfunction with emerging immunotherapies in multiple myeloma, the impact of COVID-19, and endothelial protection with a focus on the evolving role of defibrotide.

Bispecific antibody CAR T-cell therapy COVID-19 Cytokine release syndrome Immune effector cell-associated neurotoxicity syndrome Multiple myeloma

Journal

Blood reviews
ISSN: 1532-1681
Titre abrégé: Blood Rev
Pays: England
ID NLM: 8708558

Informations de publication

Date de publication:
03 Jun 2024
Historique:
received: 01 05 2024
revised: 31 05 2024
accepted: 31 05 2024
medline: 9 6 2024
pubmed: 9 6 2024
entrez: 9 6 2024
Statut: aheadofprint

Résumé

Patients with multiple myeloma (MM) were among the groups impacted more severely by the COVID-19 pandemic, with higher rates of severe disease and COVID-19-related mortality. MM and COVID-19, plus post-acute sequelae of SARS-CoV-2 infection, are associated with endothelial dysfunction and injury, with overlapping inflammatory pathways and coagulopathies. Existing treatment options for MM, notably high-dose therapy with autologous stem cell transplantation and novel chimeric antigen receptor (CAR) T-cell therapies and bispecific T-cell engaging antibodies, are also associated with endothelial cell injury and mechanism-related toxicities. These pathologies include cytokine release syndrome (CRS) and neurotoxicity that may be exacerbated by underlying endotheliopathies. In the context of these overlapping risks, prophylaxis and treatment approaches mitigating the inflammatory and pro-coagulant effects of endothelial injury are important considerations for patient management, including cytokine receptor antagonists, thromboprophylaxis with low-molecular-weight heparin and direct oral anticoagulants, and direct endothelial protection with defibrotide in the appropriate clinical settings.

Identifiants

pubmed: 38852017
pii: S0268-960X(24)00051-1
doi: 10.1016/j.blre.2024.101218
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

101218

Informations de copyright

Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest C.C.M.: Advisory boards for AbbVie, Bristol Myers Squibb, GSK, Janssen, Karyopharm, Sanofi, and Takeda; consultancy for AbbVie, Janssen, Karyopharm, and Sanofi. E.R.: None. E.C.: None. F.C.: None. M.H.K.: Grants to institution for clinical trials from Bristol Myers Squibb/Celgene, Janssen, AbbVie, Arcellx/Kite, Roche and Poseida Therapeutics. R.M.B.: None. J.M.C.: Consulting and scientific advisory boards for Abbott, Anthos, Bristol Myers Squibb, Roche, Sanofi, and Werfen; research funding to the institution from CSL Behring. M.I.: None. L.-J.W.: None. A.P.R.: None. M.D.-R.: Speaker fees from Jazz Pharmaceuticals and research funding to institution from Novartis Spain, CSL Behring, and Sysmex Europe GmbH. J.M.M.: Research support from Pfizer, Gilead, Novartis, Bristol Myers Squibb, Amgen, and Roche, and advisory committees for Rocket Pharma, Jazz Pharma, Novartis, Gilead, and Sandoz. C.C.-S.: Consultancy with Sanofi, membership of the board of directors, speakers bureau, or advisory committee for ADC Therapeutics SA, Bristol Myers Squibb, Celgene, Karyopharm, Roche, and Sanofi; research funding from ADC Therapeutics SA, Roche, and Sanofi; honoraria from ADC Therapeutics SA, AstraZeneca, Bristol Myers Squibb, Incyte, Janssen Oncology, and Takeda. P.G.R.: Grants to institution for clinical trials from Bristol Myers Squibb / Celgene, Karyopharm, and Oncopeptides; advisory committees for Bristol Myers Squibb / Celgene, GSK, Karyopharm, Oncopeptides, Adaptive Biotechnologies, and Sanofi.

Auteurs

Clifton C Mo (CC)

Department of Medical Oncology, Dana-Farber Cancer Institute, Jerome Lipper Center for Multiple Myeloma Research, Harvard Medical School, Boston, MA, USA.

Edward Richardson (E)

Department of Medicine, Warren Alpert Medical School at Brown University, Providence, RI, USA.

Eleonora Calabretta (E)

Department of Biomedical Sciences, Humanitas University, and IRCCS Humanitas Research Hospital, Milan, Italy; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.

Francesco Corrado (F)

Department of Medical Oncology, Dana-Farber Cancer Institute, Jerome Lipper Center for Multiple Myeloma Research, Harvard Medical School, Boston, MA, USA; Department of Biomedical Sciences, Humanitas University, and IRCCS Humanitas Research Hospital, Milan, Italy; Broad Institute of Massachusetts Institute of Technology (MIT) and Harvard, Cambridge, MA, USA.

Mehmet H Kocoglu (MH)

Department of Medicine, University of Maryland School of Medicine, and Transplant and Cellular Therapy Program, University of Maryland Greenebaum Comprehensive Cancer Center, Baltimore, MD, USA.

Rebecca M Baron (RM)

Division of Pulmonary and Critical Care Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

Jean Marie Connors (JM)

Division of Hematology, Brigham and Women's Hospital, Boston, MA, USA.

Massimo Iacobelli (M)

Techitra S.r.l., Milan, Italy.

Lee-Jen Wei (LJ)

Department of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA, USA.

Aaron P Rapoport (AP)

Department of Medicine, University of Maryland School of Medicine, and Transplant and Cellular Therapy Program, University of Maryland Greenebaum Comprehensive Cancer Center, Baltimore, MD, USA.

Maribel Díaz-Ricart (M)

Hematopathology, Pathology Department, CDB, Hospital Clinic, and IDIBAPS, Barcelona, Spain, and Barcelona Endothelium Team, Barcelona, Spain.

José M Moraleda (JM)

Department of Medicine, Faculty of Medicine, Institute of Biomedical Research (IMIB-Pascual Parrilla), University of Murcia, Murcia, Spain.

Carmelo Carlo-Stella (C)

Department of Biomedical Sciences, Humanitas University, and IRCCS Humanitas Research Hospital, Milan, Italy.

Paul G Richardson (PG)

Department of Medical Oncology, Dana-Farber Cancer Institute, Jerome Lipper Center for Multiple Myeloma Research, Harvard Medical School, Boston, MA, USA. Electronic address: Paul_Richardson@dfci.harvard.edu.

Classifications MeSH