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Published on: May 7, 2012
Safety and tolerability of cidofovir in high-risk pediatric patients
V A Bhadri1, L Lee-Horn, P J Shaw
1Oncology, Children's Hospital at Westmead, New South Wales, Australia.
Insights
Cidofovir is a primary treatment for adenovirus infections post-hematopoietic stem cell transplant. This study shows cidofovir is safe and well-tolerated in pediatric patients, with acceptable kidney safety despite other medications.
Area of Science:
- Hematology
- Infectious Diseases
- Pediatric Oncology
Background:
- Adenovirus (ADV) infection poses a significant threat after hematopoietic stem cell transplantation (HSCT), leading to considerable illness and death.
- Cidofovir is the main treatment for ADV infections, but potential kidney toxicity restricts its use.
Purpose of the Study:
- To evaluate the safety and tolerability of cidofovir in pediatric patients undergoing HSCT.
- To assess the incidence of nephrotoxicity associated with cidofovir treatment in this high-risk population.
Main Methods:
- Retrospective analysis of 234 cidofovir infusions administered to 23 pediatric patients at a single institution.
- Monitoring for adverse events, including nephrotoxicity, during cidofovir therapy.
- Evaluation of concomitant use of other nephrotoxic agents.
Main Results:
- Cidofovir was administered safely across 234 infusions in 23 pediatric patients.
- Adverse events were infrequent, with only three patients experiencing issues, two linked to the hydration protocol.
- Evidence suggests acceptable kidney safety, even with concurrent use of other nephrotoxic medications.
Conclusions:
- Cidofovir demonstrates a favorable safety and tolerability profile in pediatric patients at high risk post-HSCT.
- The drug can be administered with acceptable kidney safety, mitigating concerns about nephrotoxicity in this vulnerable group.
Abstract:
Adenovirus (ADV) infection is a serious complication after hematopoietic stem cell transplantation with significant morbidity and mortality. Cidofovir has emerged as the primary therapy for ADV infection, but its use has been limited by concerns of nephrotoxicity. We report the safety and tolerability of 234 cidofovir infusions in 23 patients at a single institution, and demonstrate evidence of acceptable nephrotoxicity despite concomitant use of other nephrotoxic agents. Three patients suffered adverse events, two related to the hydration regimen associated with cidofovir administration. We conclude that cidofovir is a safe and mostly well tolerated drug in a high-risk pediatric population.
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