Sequential treatment of cytomegalovirus infection or disease with a short course of intravenous ganciclovir followed by oral valganciclovir: efficacy, safety, and pharmacokinetics
- PMID: 20002612
- DOI: 10.1111/j.1399-3062.2009.00481.x
Sequential treatment of cytomegalovirus infection or disease with a short course of intravenous ganciclovir followed by oral valganciclovir: efficacy, safety, and pharmacokinetics
Abstract
Oral (p.o.) or intravenous (IV) ganciclovir (GCV) has been the first-line agent for prevention and treatment of cytomegalovirus (CMV) infection and disease in solid organ transplantation (SOT). The introduction of p.o. valganciclovir, with higher bioavailability than p.o. GCV, has proven to be a suitable approach toward outpatient p.o. therapy for CMV infection/disease. The present single-arm, exploratory pilot trial performed with 21 patients investigates the efficacy and safety of a short therapeutic course (21 days) based on an initial IV treatment with GCV (5 mg/kg twice daily, for 5 days) followed by p.o. valganciclovir (900 mg twice daily, for 16 days) for CMV infection/disease in SOT patients. In all cases, doses were adjusted for renal function. Moreover, the study allowed comparison of exposure to GCV after p.o. valganciclovir with respect to IV GCV in the same patients. Response to treatment was monitored until day 180. Viral load eradication was achieved in 66.7% of patients, on day 21. Although not statistically significant, a trend was seen toward increased persistence of viral load on day 21 for patients with donor positive/recipient negative CMV serostatus or receiving either anti-rejection therapy or polyclonal anti-thymocyte globulin. CMV clinical infection recurred in 14.3% of patients, with higher recurrence rates in patients with risk factors for persistence of viremia. Exposures to GCV after using IV GCV or p.o. valganciclovir showed comparable values (P=0.054). This short course, combining initial IV GCV and subsequent p.o. valganciclovir, may provide effective exposure and therapeutic response in the treatment of CMV infection in SOT patients with adequate drug exposure and with the additional potential benefit of shortening the length of hospital stay, which may result in cost reduction and improved patient comfort.
Similar articles
-
Similar reduction of cytomegalovirus DNA load by oral valganciclovir and intravenous ganciclovir on pre-emptive therapy after renal and renal-pancreas transplantation.Antivir Ther. 2005;10(1):119-23. Antivir Ther. 2005. PMID: 15751769 Clinical Trial.
-
Valganciclovir prophylaxis versus preemptive therapy in cytomegalovirus-positive renal allograft recipients: 1-year results of a randomized clinical trial.Transplantation. 2012 Jan 15;93(1):61-8. doi: 10.1097/TP.0b013e318238dab3. Transplantation. 2012. PMID: 22094954 Clinical Trial.
-
Cytomegalovirus resistance in solid organ transplant recipients treated with intravenous ganciclovir or oral valganciclovir.Antivir Ther. 2009;14(5):697-704. Antivir Ther. 2009. PMID: 19704173 Clinical Trial.
-
Oral valganciclovir versus ganciclovir as delayed pre-emptive therapy for patients after allogeneic hematopoietic stem cell transplant: a pilot trial (04-0274) and review of the literature.Transpl Infect Dis. 2012 Jun;14(3):259-67. doi: 10.1111/j.1399-3062.2011.00689.x. Epub 2011 Oct 28. Transpl Infect Dis. 2012. PMID: 22093134 Review.
-
Valganciclovir: therapeutic role in pediatric solid organ transplant recipients.Expert Opin Pharmacother. 2013 Apr;14(6):807-15. doi: 10.1517/14656566.2013.778244. Epub 2013 Mar 8. Expert Opin Pharmacother. 2013. PMID: 23469871 Review.
Cited by
-
Comparison of Three Renal Function Formulas for Ganciclovir/Valganciclovir Dose Individualization in CMV-Infected Solid Organ Transplantation Patients Using a Population Approach.Clin Pharmacokinet. 2023 Jun;62(6):861-880. doi: 10.1007/s40262-023-01237-3. Epub 2023 May 4. Clin Pharmacokinet. 2023. PMID: 37140726 Free PMC article.
-
Optimization of Thymidine Kinase-Based Safety Switch for Neural Cell Therapy.Cells. 2022 Jan 31;11(3):502. doi: 10.3390/cells11030502. Cells. 2022. PMID: 35159311 Free PMC article.
-
Cytomegalovirus Treatment.Curr Treat Options Infect Dis. 2014;6(3):256-270. doi: 10.1007/s40506-014-0021-5. Curr Treat Options Infect Dis. 2014. PMID: 25999800 Free PMC article. Review.
-
Contribution of Population Pharmacokinetics to Dose Optimization of Ganciclovir-Valganciclovir in Solid-Organ Transplant Patients.Antimicrob Agents Chemother. 2016 Mar 25;60(4):1992-2002. doi: 10.1128/AAC.02130-15. Print 2016 Apr. Antimicrob Agents Chemother. 2016. PMID: 26824942 Free PMC article. Clinical Trial.
-
Serum ganciclovir drug exposure in children receiving standard ganciclovir dosing.Antimicrob Agents Chemother. 2024 Oct 8;68(10):e0052524. doi: 10.1128/aac.00525-24. Epub 2024 Sep 18. Antimicrob Agents Chemother. 2024. PMID: 39291998 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical