Optimizing pegylated asparaginase use: An institutional guideline for dosing, monitoring, and management

Author:

Bade Najeebah A12,Lu Crystal2ORCID,Patzke Ciera L34,Baer Maria R12,Duong Vu H12,Law Jennie Y12,Lee Seung T12,Sausville Edward A12,Zimrin Ann B12,Duffy Alison P25,Lawson Justin2,Emadi Ashkan12

Affiliation:

1. Division of Hematology/Oncology, Department of Medicine, University of Maryland School of Medicine, Baltimore, MD, USA

2. Marlene and Stewart Greenebaum Comprehensive Cancer Center, University of Maryland School of Medicine, Baltimore, MD, USA

3. Department of Pharmacy Practice and Administration, Ernest Mario School of Pharmacy at Rutgers, The State University of New Jersey, Piscataway, NJ, USA

4. Department of Pharmacy, Hackensack University Medical Center, Hackensack, NJ, USA

5. Department of Pharmacy Practice, University of Maryland School of Pharmacy, Baltimore, MD, USA

Abstract

The incorporation of L-asparaginase and pegylated asparaginase into pediatric-inspired regimens has conferred a survival advantage in treatment of adults with acute lymphoblastic leukemia. Use of asparaginase products requires careful prevention, monitoring, and management of adverse effects including hypersensitivity, hepatotoxicity, pancreatitis, coagulopathy, and thrombosis. Currently, there is limited published literature to offer guidance on management of these toxicities. At the University of Maryland Marlene and Stewart Greenebaum Comprehensive Cancer Center, a standard of practice guideline was created to prevent and manage asparaginase-related adverse events. By sharing our long-term experience with asparaginase products and clinical management of asparaginase-induced toxicities, this article aims to improve patient safety and optimize treatment outcomes.

Publisher

SAGE Publications

Subject

Pharmacology (medical),Oncology

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