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Use of allopurinol to manage skewed 6-mercaptopurine metabolism in pediatric maintenance acute lymphoblastic leukemia treatment.
Lines, Mandee; Kemper, Ryan M; Wallace, Jordan; Alexander, Thomas; Echols, Carmen; Garner, Lauren M; Kaplan, Jenna Bognaski; Thompson, Patrick; Crona, Daniel J; Phillips, Kynlon.
Afiliação
  • Lines M; Department of Pharmacy, University of North Carolina Medical Center, Chapel Hill, North Carolina, USA.
  • Kemper RM; Division of Pharmacotherapy and Experimental Therapeutics, UNC Eshelman School of Pharmacy, Chapel Hill, North Carolina, USA.
  • Wallace J; Department of Pharmacy, Golisano Children's Hospital, Fort Myers, Florida, USA.
  • Alexander T; Department of Pediatric Hematology/Oncology, University of North Carolina Medical Center, Chapel Hill, North Carolina, USA.
  • Echols C; UNC Lineberger Comprehensive Cancer Center, Chapel Hill, North Carolina, USA.
  • Garner LM; Department of Pharmacy, University of North Carolina Medical Center, Chapel Hill, North Carolina, USA.
  • Kaplan JB; Department of Pharmacy, University of North Carolina Medical Center, Chapel Hill, North Carolina, USA.
  • Thompson P; Department of Pharmacy, University of North Carolina Medical Center, Chapel Hill, North Carolina, USA.
  • Crona DJ; Department of Pediatric Hematology/Oncology, University of North Carolina Medical Center, Chapel Hill, North Carolina, USA.
  • Phillips K; UNC Lineberger Comprehensive Cancer Center, Chapel Hill, North Carolina, USA.
Eur J Haematol ; 2024 Jul 11.
Article em En | MEDLINE | ID: mdl-38989562
ABSTRACT

BACKGROUND:

6-mercaptopurine is a cornerstone of maintenance therapy for pediatric ALL. Response to 6MP is typically determined by the ANC. Therapeutic ANC range while receiving 6MP is between 500 and 1500/µL. In addition to desired myelosuppression, 6MP is associated with multiple adverse drug effects. Increased doses of 6MP can lead to therapeutic ANC values; however, patients may experience adverse effects before obtaining therapeutic myelosuppression, often deemed "skewed metabolism." Allopurinol may potentially correct skewed 6MP metabolism. PROCEDURE Pediatric patients with ALL with 6MMP and 6TGN metabolites drawn during maintenance therapy were analyzed for allopurinol use. The primary outcome evaluated the percentage of time spent in therapeutic ANC range before and after allopurinol initiation. In addition, the difference in 6MMP6TGN ratios before and after allopurinol initiation, incidence of hepatotoxicity, and rates of relapse, were analyzed.

RESULTS:

Ninety-five patients were included for analysis. Thirty-two (34%) patients received allopurinol. There were no significant differences in baseline demographics between the patients who received allopurinol and those who did not. When comparing ANC values pre- and post-allopurinol initiation, a statistically significant increase in the percentage of time spent in therapeutic range was observed (27% vs. 43%; p = .03). In addition, when comparing metabolite ratios pre- and post-allopurinol initiation, a statistically significant decrease in 6MMP6TGN metabolite ratio values was observed (86.7 vs. 3.6; p < .0001).

CONCLUSIONS:

Allopurinol significantly increased the percent time in therapeutic ANC range and can be safely utilized to significantly lower the ratio of 6MMP6TGN metabolites, alleviating the undesirable side effects of 6MMP, and optimizing the anti-leukemic effects associated with 6TGN.
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Texto completo: 1 Coleções: 01-internacional Temas: Geral / Tipos_de_cancer / Leucemia Base de dados: MEDLINE Idioma: En Revista: Eur J Haematol Assunto da revista: HEMATOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Temas: Geral / Tipos_de_cancer / Leucemia Base de dados: MEDLINE Idioma: En Revista: Eur J Haematol Assunto da revista: HEMATOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos