SOHO State of the Art Updates and Next Questions | Asparaginase—Understanding and Overcoming Toxicities in Adults with ALL

The adoption of pediatric-inspired regimens in young adults with newly diagnosed acute lymphoblastic leukemia (ALL) has significantly improved their survival outcomes. Pediatric-inspired regimens in ALL rely profoundly on delivering adequate dosing of non-myelosuppressive drugs of which asparaginase...

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Veröffentlicht in:Clinical lymphoma, myeloma and leukemia myeloma and leukemia, 2022-11, Vol.22 (11), p.787-794
Hauptverfasser: Aldoss, Ibrahim, Pourhassan, Hoda, Douer, Dan
Format: Artikel
Sprache:eng
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Zusammenfassung:The adoption of pediatric-inspired regimens in young adults with newly diagnosed acute lymphoblastic leukemia (ALL) has significantly improved their survival outcomes. Pediatric-inspired regimens in ALL rely profoundly on delivering adequate dosing of non-myelosuppressive drugs of which asparaginase, a bacterial derived agent, is a key component. Asparaginase therapy is associated with a spectrum of unique toxicities that are observed more frequently in adult patients compared to children with ALL, and this observation has contributed to the reluctance of adult oncologists to administer the drug to their patients. Understanding the breadth of asparaginase toxicity and the associated risk factors may help in preventing severe manifestations and allow safer treatment for adults with ALL. In this review, we will discuss the different formulations of asparaginase and the appropriate dosing in adults with ALL. We will further discuss the frequency and risk factors for individual toxicities of asparaginase along with strategies for their prevention and management. Asparaginase is a key element in modern frontline therapeutic regimens in young adults with acute lymphoblastic leukemia. Asparaginase has a unique spectrum of toxicities, however, they are usually reversible and manageable. Herein, we discuss asparaginase toxicities and our approach for prevention and management.
ISSN:2152-2650
2152-2669
DOI:10.1016/j.clml.2022.08.009