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Drug Resistance Assessed in a Phase 3 Clinical Trial of Maribavir Therapy for Refractory or Resistant Cytomegalovirus Infection in Transplant Recipients
被引:45
作者:
Chou, Sunwen
[1
,2
,14
]
Alain, Sophie
[3
,4
]
Cervera, Carlos
[5
]
Chemaly, Roy F.
[6
]
Kotton, Camille N.
[7
]
Lundgren, Jens
[8
]
Papanicolaou, Genovefa A.
[9
,10
]
Pereira, Marcus R.
[11
]
Wu, Jingyang J.
[12
]
Murray, Rose Ann
[12
]
Buss, Neil E.
[13
]
Fournier, Martha
[12
,15
]
机构:
[1] Oregon Hlth & Sci Univ, Div Infect Dis, Portland, OR USA
[2] Vet Affairs Portland Hlth Care Syst, Res & Dev Serv, Portland, OR USA
[3] Univ Limoges, Limoges Univ Hosp, Dept Virol, Limoges, France
[4] Univ Limoges, Limoges Univ Hosp, Natl Reference Ctr Herpesviruses, Inserm,UMR 1092, Limoges, France
[5] Univ Alberta, Dept Med, Div Infect Dis, Edmonton, AB, Canada
[6] Univ Texas MD Anderson Canc Ctr, Dept Infect Dis Infect Control & Employee Hlth, Houston, TX USA
[7] Harvard Med Sch, Massachusetts Gen Hosp, Infect Dis Div, Transplant & Immunocompromised Host Infect Dis, Boston, MA USA
[8] Univ Copenhagen, Rigshosp, Ctr Hlth & Infect Dis Res, Dept Infect Dis, Copenhagen, Denmark
[9] Mem Sloan Kettering Canc Ctr, Dept Med, Infect Dis Serv, New York, NY USA
[10] Weill Cornell Med, Dept Med, New York, NY USA
[11] Columbia Univ, Med Ctr, Dept Med, New York, NY USA
[12] Takeda Dev Ctr Amer Inc, Lexington, MA USA
[13] Med Express, Solothurn, Switzerland
[14] Oregon Hlth & Sci Univ, Div Infect Dis L457, 3181 SW Sam Jackson Pk Rd, Portland, OR 97239 USA
[15] Takeda Dev Ctr Amer Inc, 300 Shire Way, Lexington, MA 02421 USA
基金:
美国国家卫生研究院;
关键词:
antiviral drug resistance;
antiviral therapy;
cytomegalovirus;
maribavir;
IN-VITRO;
MUTATIONS;
GANCICLOVIR;
LETERMOVIR;
INHIBITION;
EVOLUTION;
KINASE;
D O I:
10.1093/infdis/jiad293
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Background This drug resistance analysis of a randomized trial includes 234 patients receiving maribavir and 116 receiving investigator-assigned standard therapy (IAT), where 56% and 24%, respectively, cleared cytomegalovirus DNA at week 8 (treatment responders).Methods Baseline and posttreatment plasma samples were tested for mutations conferring drug resistance in viral genes UL97, UL54, and UL27.Results At baseline, genotypic testing revealed resistance to ganciclovir, foscarnet, or cidofovir in 56% of patients receiving maribavir and 68% receiving IAT, including 9 newly phenotyped mutations. Among them, 63% (maribavir) and 21% (IAT) were treatment responders. Detected baseline maribavir resistance mutations were UL27 L193F (n = 1) and UL97 F342Y (n = 3). Posttreatment, emergent maribavir resistance mutations were detected in 60 (26%) of those randomized to maribavir, including 49 (48%) of 103 nonresponders and 25 (86%) of the 29 nonresponders where viral DNA initially cleared then rebounded while on maribavir. The most common maribavir resistance mutations were UL97 T409M (n = 34), H411Y (n = 26), and C480F (n = 21), first detected 26 to 130 (median 56) days after starting maribavir.Conclusions Baseline maribavir resistance was rare. Drug resistance to standard cytomegalovirus antivirals did not preclude treatment response to maribavir. Rebound in plasma cytomegalovirus DNA while on maribavir strongly suggests emerging drug resistance.Clinical Trials Registration NCT02931539. Resistance to existing cytomegalovirus antiviral therapy did not preclude a treatment response to maribavir. Emergent maribavir resistance developed in 26% of 234 treated patients including 86% of 29 patients where viral DNA initially cleared then rebounded while on maribavir.
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页码:413 / 421
页数:9
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