Impact of Black Race on Peripheral Neuropathy in Patients With Newly Diagnosed Multiple Myeloma Receiving Bortezomib Induction.


Journal

JCO oncology practice
ISSN: 2688-1535
Titre abrégé: JCO Oncol Pract
Pays: United States
ID NLM: 101758685

Informations de publication

Date de publication:
09 2023
Historique:
pmc-release: 01 09 2024
medline: 14 9 2023
pubmed: 7 7 2023
entrez: 7 7 2023
Statut: ppublish

Résumé

The incidence of multiple myeloma (MM) is two to three times higher in Black patients compared with other races, making it the most common hematologic malignancy in this patient population. Current treatment guidelines recommend the combination of a proteasome inhibitor, an immunomodulatory agent, and a corticosteroid as preferred induction therapy. Bortezomib use comes with the risk of peripheral neuropathy (PN) and potential need for dose reduction, therapy interruption, and additional supportive medications. Known risk factors for bortezomib-induced peripheral neuropathy (BIPN) include diabetes mellitus, previous thalidomide, advanced age, and obesity. We aimed to determine the potential association between Black race and incidence of BIPN. We identified a cohort of 748 patients with newly diagnosed MM who received induction with bortezomib, lenalidomide, and dexamethasone from 2007 to 2016. One hundred forty Black patients were matched with 140 non-Black patients on age, sex, BMI, and route of bortezomib administration. Incidence of BIPN was a binary event defined as new use of a neuropathy medication, bortezomib dose reduction, dose omission, or discontinuation because of PN. The incidence of BIPN was higher in Black patients (46%) compared with non-Black patients (34%; These data indicate that Black race is an independent risk factor for the development of BIPN. Additional prevention strategies, close monitoring, and appropriate supportive care measures are warranted for these patients.

Identifiants

pubmed: 37418682
doi: 10.1200/OP.22.00781
pmc: PMC10538896
doi:

Substances chimiques

Bortezomib 69G8BD63PP
Lenalidomide F0P408N6V4
Thalidomide 4Z8R6ORS6L

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

793-798

Subventions

Organisme : NCI NIH HHS
ID : P30 CA138292
Pays : United States

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Auteurs

Laura F Sun (LF)

Department of Pharmacy, Winship Cancer Institute of Emory University, Atlanta, GA.

Kathryn T Maples (KT)

Department of Pharmacy, Winship Cancer Institute of Emory University, Atlanta, GA.

Kevin H Hall (KH)

Department of Pharmacy, Winship Cancer Institute of Emory University, Atlanta, GA.

Yuan Liu (Y)

Department of Biostatistics and Bioinformatics, Winship Cancer Institute of Emory University, Atlanta, GA.

Yichun Cao (Y)

Department of Biostatistics and Bioinformatics, Winship Cancer Institute of Emory University, Atlanta, GA.

Nisha S Joseph (NS)

Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA.

Craig C Hofmeister (CC)

Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA.

Jonathan L Kaufman (JL)

Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA.

Madhav Dhodapkar (M)

Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA.

Ajay K Nooka (AK)

Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA.

Sagar Lonial (S)

Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA.

R Donald Harvey (RD)

Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA.
Department of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, GA.

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Classifications MeSH