Nelarabine: When, Where and How to Use it When Treating T-cell Acute Lymphoblastic Leukemia.


Journal

Blood advances
ISSN: 2473-9537
Titre abrégé: Blood Adv
Pays: United States
ID NLM: 101698425

Informations de publication

Date de publication:
30 Jun 2023
Historique:
accepted: 28 06 2023
received: 31 05 2023
revised: 27 06 2023
medline: 30 6 2023
pubmed: 30 6 2023
entrez: 30 6 2023
Statut: aheadofprint

Résumé

T-cell acute lymphoblastic leukemia or lymphoblastic lymphoma (T-ALL/LBL) is a rare hematologic malignancy most commonly affecting adolescent and young adult (AYA) males. Outcomes are dismal for patients who relapse so improvement in treatment is needed. Nelarabine, a pro-drug of the deoxyguanosine analogue ara-G, is uniquely toxic to T-lymphoblasts, compared to B-lymphoblasts and normal lymphocytes, and has been developed for the treatment of T-ALL/LBL. Based on phase I and II trials in children and adults, single-agent nelarabine is approved for treatment of patients with R/R T-ALL/LBL, with the major adverse effect being central and peripheral neurotoxicity. Since its approval in 2005, nelarabine has been studied in combination with other chemotherapy agents for relapsed disease and is also being studied as a component of initial treatment in pediatric and adult patients. Here, we review current data with nelarabine and present our approach to the use of nelarabine in the treatment of patients with T-ALL/LBL.

Identifiants

pubmed: 37389830
pii: 496638
doi: 10.1182/bloodadvances.2023010303
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2023 American Society of Hematology.

Auteurs

Shai Shimony (S)

Dana-Farber Cancer Institute, Boston, Massachusetts, United States.

Daniel J DeAngelo (DJ)

Dana-Farber Cancer Institute, Boston, Massachusetts, United States.

Marlise R Luskin (MR)

Dana-Farber Cancer Institute, Boston, Massachusetts, United States.

Classifications MeSH