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Original Article: Clinical

Levocarnitine for asparaginase-induced hepatic injury: a multi-institutional case series and review of the literature

ORCID Icon, , , , , , & ORCID Icon show all
Pages 2360-2368 | Received 04 Oct 2017, Accepted 23 Jan 2018, Published online: 12 Feb 2018
 

Abstract

Asparaginase, an important treatment component for acute lymphoblastic leukemia (ALL), causes severe hepatotoxicity in some patients. Levocarnitine is a mitochondrial co-factor that can potentially ameliorate the mitochondrial toxicity of asparaginase. In this retrospective case series, we describe the clinical presentation and management of six pediatric and young adult patients (mean age 12.7, range 9–24 years) with ALL who developed Grade 3–4 hyperbilirubinemia following administration of asparaginase as part of induction/re-induction therapy. Five of these patients were treated with levocarnitine with subsequent improvement of hyperbilirubinemia, while one patient was given levocarnitine prophylactically during induction and developed Grade 3 hyperbilirubinemia, but did not require therapy adjustments or delays. Increased awareness in the pediatric oncology community regarding asparaginase-associated hepatic toxicity and the potential role of levocarnitine in management is warranted.

Acknowledgements

M. J. B. is the Consultant for Shire Pharmaceuticals, JAZZ Pharmaceuticals, Speaker’s Bureau for Shire Pharmaceuticals and JAZZ Pharmaceuticals.

Potential conflict of interest

Disclosure forms provided by the authors are available with the full text of this article online at https://doi.org/10.1080/10428194.2018.1435873.

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