Guidelines for the Use of Antiretroviral Agents in Pediatric HIV Infection
Entry and Fusion Inhibitors
Last Updated: April 27, 2017; Last Reviewed: April 27, 2017
|Enfuvirtide (T-20, Fuzeon)
For additional information see Drugs@FDA: http://www.accessdata.fda.gov/scripts/cder/daf/
Lyophilized Powder for Injection:
|Dosing Recommendations||Selected Adverse Events|
Pediatric and Adolescent Dose (Aged 6–16 Years)
Children Aged <6 Years:
Drug Interactions (see also the Guidelines for the Use of Antiretroviral Agents in HIV-1-Infected Adults and Adolescents and http://www.hiv-druginteractions.org/)
- There are no known significant drug interactions with enfuvirtide.
- More common: Almost all patients (87% to 98%) experience local injection site reactions including pain and discomfort, induration, erythema, nodules and cysts, pruritus, and ecchymosis. Reactions are usually mild to moderate in severity but can be more severe. Average duration of local injection site reaction is 3 to 7 days, but was >7 days in 24% of patients.
- Less common (more severe): Increased rate of bacterial pneumonia (unclear association).1 Pediatric studies have lacked the statistical power to answer questions concerning enfuvirtide use and increased risk of pneumonia.
- Rare: Hypersensitivity reactions (HSRs) (<1%) including fever, nausea and vomiting, chills, rigors, hypotension, and elevated liver transaminases; immune-mediated reactions including primary immune complex reaction, respiratory distress, glomerulonephritis, and Guillain-Barre syndrome. Patients experiencing HSRs should seek immediate medical attention. Therapy should not be restarted in patients with signs and symptoms consistent with HSRs.
- Pediatric specific: Local site cellulitis requiring antimicrobial therapy (up to 11% in certain subgroups of patients in pediatric studies).2
The International Antiviral Society-USA (IAS-USA) maintains a list of updated resistance mutations (see http://iasusa.org/sites/default/files/tam/october_november_2015.pdf#page=10) and the Stanford University HIV Drug Resistance Database offers a discussion of each mutation (see http://hivdb.stanford.edu/DR/).
Resistance testing must be ordered specifically for fusion inhibitors, as it is not performed on routine genotypic or phenotypic assays.
Although enfuvirtide is Food and Drug Administration (FDA)-approved for use in children, it is not commonly used because of its high cost, need for twice-daily subcutaneous (SQ) injections, and high rate of injection site reactions. Use in deep salvage regimens3 has also declined with the availability of integrase inhibitors and other entry inhibitors (such as maraviroc).
A single-dose pharmacokinetic evaluation study of enfuvirtide, given SQ to 14 children with HIV infection aged 4 to 12 years (PACTG 1005), identified that enfuvirtide 60 mg/m2 of body surface area per dose resulted in a target trough concentration that approximated the equivalent of a 90-mg dose delivered SQ to an adult (1000 mg/mL).4 In a second pediatric study of 25 children aged 5 to 16 years, a 2-mg/kg dose (maximum 90 mg) of enfuvirtide given twice daily yielded drug concentrations similar to 60 mg/m2 of body surface area dose independent of age group, body weight, body surface area, and sexual maturation.5 The FDA-recommended dose of enfuvirtide for children aged 6 to 16 years is 2 mg/kg (maximum 90 mg) administered SQ twice daily. Further data are needed for dosing in children aged <6 years.
- Kousignian I, Launay O, Mayaud C, et al. Does enfuvirtide increase the risk of bacterial pneumonia in patients receiving combination antiretroviral therapy? J Antimicrob Chemother. 2010;65(1):138-144. Available at http://www.ncbi.nlm.nih.gov/pubmed/19903719.
- Wiznia A, Church J, Emmanuel P, et al. Safety and efficacy of enfuvirtide for 48 weeks as part of an optimized antiretroviral regimen in pediatric human immunodeficiency virus 1-infected patients. Pediatr Infect Dis J. 2007;26(9):799-805. Available at http://www.ncbi.nlm.nih.gov/pubmed/17721374.
- Feiterna-Sperling C, Walter H, Wahn V, Kleinkauf N. A 12-year-old boy with multidrug-resistant human immunodeficiency virus type 1 successfully treated with HAART including ritonavir-boosted tipranavir oral solution and enfuvirtide. Eur J Med Res. 2009;14(1):44-46. Available at http://www.ncbi.nlm.nih.gov/pubmed/19258211.
- Church JA, Cunningham C, Hughes M, et al. Safety and antiretroviral activity of chronic subcutaneous administration of T-20 in human immunodeficiency virus 1-infected children. Pediatr Infect Dis J. 2002;21(7):653-659. Available at http://www.ncbi.nlm.nih.gov/pubmed/12237598.
- Bellibas SE, Siddique Z, Dorr A, et al. Pharmacokinetics of enfuvirtide in pediatric human immunodeficiency virus 1-infected patients receiving combination therapy. Pediatr Infect Dis J. 2004;23(12):1137-1141. Available at http://www.ncbi.nlm.nih.gov/pubmed/15626952.
- Church JA, Hughes M, Chen J, et al. Long term tolerability and safety of enfuvirtide for human immunodeficiency virus 1-infected children. Pediatr Infect Dis J. 2004;23(8):713-718. Available at http://www.ncbi.nlm.nih.gov/pubmed/15295220.