Drug Resistance Mutations and Associated Phenotypes Detected in Clinical Trials of Maribavir for Treatment of Cytomegalovirus Infection. (29th July 2020)
- Record Type:
- Journal Article
- Title:
- Drug Resistance Mutations and Associated Phenotypes Detected in Clinical Trials of Maribavir for Treatment of Cytomegalovirus Infection. (29th July 2020)
- Main Title:
- Drug Resistance Mutations and Associated Phenotypes Detected in Clinical Trials of Maribavir for Treatment of Cytomegalovirus Infection
- Authors:
- Chou, Sunwen
Song, Kening
Wu, Jingyang
Bo, Tien
Crumpacker, Clyde - Abstract:
- Abstract: Background: In separate phase 2 trials, 120 patients received maribavir for cytomegalovirus (CMV) infection failing conventional therapy (trial 202) and 119 received maribavir for asymptomatic infection (trial 203). Overall, 172 cleared their CMV infection (CMV DNA <200 copies/mL) within 6 weeks. Methods: Baseline and posttreatment plasma samples were tested for mutations in viral genes UL97, UL54, and/or UL27 . Selected viral mutants were phenotyped for drug susceptibility. Results: Baseline samples revealed UL54 mutations newly phenotyped as conferring resistance to standard DNA polymerase inhibitor(s), including K493N, P497S, K513T, L565V, V823A, A987V, and E989D. Of 29 patients (including 25 from trial 202) who cleared but later experienced recurrent CMV infection while on maribavir, 23 had available UL97 genotyping data; 17 had known resistance mutations (T409M or H411Y) and 5 additional had UL97 C480F alone. The newly phenotyped mutation C480F conferred high-grade maribavir resistance and low-grade ganciclovir resistance. Among 25 who did not respond to >14 days of therapy, 9 showed T409M or H411Y and 4 others showed C480F alone. Conclusions: After maribavir therapy (400–1200 mg twice daily), UL97 mutations T409M, H411Y, or C480F emerge to confer maribavir resistance in patients with recurrent CMV infection while on therapy or no response to therapy. Clinical Trials Registration: NCT01611974 and EudraCT 2010-024247-32. Abstract : In phase 2 trials ofAbstract: Background: In separate phase 2 trials, 120 patients received maribavir for cytomegalovirus (CMV) infection failing conventional therapy (trial 202) and 119 received maribavir for asymptomatic infection (trial 203). Overall, 172 cleared their CMV infection (CMV DNA <200 copies/mL) within 6 weeks. Methods: Baseline and posttreatment plasma samples were tested for mutations in viral genes UL97, UL54, and/or UL27 . Selected viral mutants were phenotyped for drug susceptibility. Results: Baseline samples revealed UL54 mutations newly phenotyped as conferring resistance to standard DNA polymerase inhibitor(s), including K493N, P497S, K513T, L565V, V823A, A987V, and E989D. Of 29 patients (including 25 from trial 202) who cleared but later experienced recurrent CMV infection while on maribavir, 23 had available UL97 genotyping data; 17 had known resistance mutations (T409M or H411Y) and 5 additional had UL97 C480F alone. The newly phenotyped mutation C480F conferred high-grade maribavir resistance and low-grade ganciclovir resistance. Among 25 who did not respond to >14 days of therapy, 9 showed T409M or H411Y and 4 others showed C480F alone. Conclusions: After maribavir therapy (400–1200 mg twice daily), UL97 mutations T409M, H411Y, or C480F emerge to confer maribavir resistance in patients with recurrent CMV infection while on therapy or no response to therapy. Clinical Trials Registration: NCT01611974 and EudraCT 2010-024247-32. Abstract : In phase 2 trials of maribavir therapy, viral UL97 mutations T409M, H411Y, or C480F emerged to confer maribavir resistance in patients with recurrent CMV infection while on therapy or no response to therapy. … (more)
- Is Part Of:
- Journal of infectious diseases. Volume 226:Number 4(2022)
- Journal:
- Journal of infectious diseases
- Issue:
- Volume 226:Number 4(2022)
- Issue Display:
- Volume 226, Issue 4 (2022)
- Year:
- 2022
- Volume:
- 226
- Issue:
- 4
- Issue Sort Value:
- 2022-0226-0004-0000
- Page Start:
- 576
- Page End:
- 584
- Publication Date:
- 2020-07-29
- Subjects:
- cytomegalovirus -- maribavir -- antiviral therapy -- antiviral drug resistance -- kinase
Communicable diseases -- Periodicals
Diseases -- Causes and theories of causation -- Periodicals
Medicine -- Periodicals
Communicable Diseases -- Periodicals
Electronic journals
616.9 - Journal URLs:
- http://jid.oxfordjournals.org/content/by/year ↗
http://www.journals.uchicago.edu/JID/journal/ ↗
http://www.jstor.org/journals/00221899.html ↗
http://ukcatalogue.oup.com/ ↗ - DOI:
- 10.1093/infdis/jiaa462 ↗
- Languages:
- English
- ISSNs:
- 0022-1899
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- Legaldeposit
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