Valacyclovir and acyclovir pharmacokinetics in immunocompromised children
Lisa Bomgaars1, Patrick Thompson, Stacey Berg
1Texas Children's Cancer Center, Baylor College of Medicine, Houston, Texas, USA. lbomgaars@txccc.org
Insights
Oral valacyclovir demonstrates good bioavailability and tolerability in immunocompromised children, supporting its use for herpes zoster treatment. This study provides key pharmacokinetic data for pediatric patients.
Area of Science:
- Pharmacology and Therapeutics
- Pediatric Infectious Diseases
Background:
- Valacyclovir, an oral prodrug of acyclovir, is used for herpes simplex and zoster infections.
- Limited pharmacokinetic and safety data exist for valacyclovir in pediatric populations.
- This study addresses the need for data on acyclovir pharmacokinetics after valacyclovir administration in immunocompromised children.
Purpose of the Study:
- To describe acyclovir pharmacokinetics following oral valacyclovir in immunocompromised pediatric patients.
- To compare pharmacokinetic parameters of oral valacyclovir versus intravenous acyclovir.
- To assess the efficacy of valacyclovir in treating active herpes zoster infections in children.
Main Methods:
- Thirty-seven immunocompromised children were enrolled in two studies.
- Pharmacokinetic data were collected from 32 patients after receiving oral valacyclovir (15 mg/kg).
- Eleven patients also underwent pharmacokinetic sampling after intravenous acyclovir administration; three received valacyclovir for herpes zoster.
Main Results:
- Mean C(max) for acyclovir after oral valacyclovir was 18.8 +/- 7 microM, with a total exposure of 4,106 +/- 1,519 microM min.
- Acyclovir bioavailability from valacyclovir was approximately 64%.
- The only reported toxicity was Grade 1 nausea and emesis in five patients; two of three herpes zoster patients showed complete lesion scabbing by day 9.
Conclusions:
- Oral valacyclovir (15 mg/kg) was well-tolerated and showed excellent bioavailability in pediatric patients.
- The findings support considering oral valacyclovir for treating herpes zoster in clinically stable pediatric oncology patients.
- Further research into valacyclovir's use in pediatric populations is warranted.
Background:
Valacyclovir, an orally administered pro-drug of acyclovir, is utilized in the therapy of herpes simplex and herpes zoster infections. Little data regarding the pharmacokinetics, safety and tolerability are available for pediatric patients. This report describes acyclovir pharmacokinetics following valacyclovir administration in immunocompromised pediatric patients, compares pharmacokinetic parameters following oral valacyclovir and IV acyclovir, and provides a limited assessment of efficacy in the setting of active herpes zoster infection.
Procedure:
A total of 37 immunocompromised children were enrolled on one of two studies. Pharmacokinetic data are available for 32 patients following valacyclovir (15 mg/kg) administration, 11 of whom also had pharmacokinetic sampling following IV acyclovir administration. Three patients received valacyclovir as treatment for herpes zoster infections.
Results:
Mean (+/-SD) C(max) values for acyclovir following oral valacyclovir were 18.8 +/- 7 microM with a total exposure of 4,106 +/- 1,519 microM min. The mean bioavailability of acyclovir from valacyclovir was 64%. Grade 1 nausea and emesis, which occurred in five patients was the only valacyclovir-related toxicity. Two of the three patients treated for herpes zoster had complete scabbing of lesions by day 9.
Conclusion:
Valacyclovir (15 mg/kg) was well tolerated in pediatric patients and demonstrated excellent bioavailability. Consideration should be given to the use of oral valacyclovir for the treatment of herpes zoster in clinically stable pediatric oncology patients.
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