Publication:
Findings from a large Asian chronic hepatitis C real-life study

dc.contributor.authorSeng Gee Limen_US
dc.contributor.authorWah Wah Phyoen_US
dc.contributor.authorSamir R. Shahen_US
dc.contributor.authorKhin Maung Winen_US
dc.contributor.authorSaeed Hamiden_US
dc.contributor.authorTeerha Piratvisuthen_US
dc.contributor.authorSoek Siam Tanen_US
dc.contributor.authorYock Young Danen_US
dc.contributor.authorYin Mei Leeen_US
dc.contributor.authorTaufique Ahmeden_US
dc.contributor.authorWei Lyn Yangen_US
dc.contributor.authorKok Pun Chenen_US
dc.contributor.authorMrunal Kamaten_US
dc.contributor.authorManav Wadhawanen_US
dc.contributor.authorKaushal Madanen_US
dc.contributor.authorRajiv Mehtaen_US
dc.contributor.authorAkash Shuklaen_US
dc.contributor.authorPrashant Dhoreen_US
dc.contributor.authorChundamannil E. Eapenen_US
dc.contributor.authorPriya Abrahamen_US
dc.contributor.authorSatyendra Tyagien_US
dc.contributor.authorAbraham Koshyen_US
dc.contributor.authorAung Hlaing Bwaen_US
dc.contributor.authorWasim Jafrien_US
dc.contributor.authorShahab Abiden_US
dc.contributor.authorFakhar Ali Qazi Arisaren_US
dc.contributor.authorTewesak Tanwandeeen_US
dc.contributor.authorThing Phee Yinen_US
dc.contributor.authorHoi Poh Teeen_US
dc.contributor.authorRosaida Binti Hj Md Saiden_US
dc.contributor.authorKhean Lee Gohen_US
dc.contributor.authorShiaw Hooi Hoen_US
dc.contributor.authorRosmawati Mohameden_US
dc.contributor.authorNorasiah Abu Bakaren_US
dc.contributor.otherNational University Health Systemen_US
dc.contributor.otherKhoo Teck Puat Hospitalen_US
dc.contributor.otherThe Aga Khan Universityen_US
dc.contributor.otherYong Loo Lin School of Medicineen_US
dc.contributor.otherFortis Escorts Heart Institute & Research Centreen_US
dc.contributor.otherUniversity of Malaya Medical Centreen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherPrince of Songkla Universityen_US
dc.contributor.otherTan Tock Seng Hospitalen_US
dc.contributor.otherLokmanya Tilak Municipal Medical Collegeen_US
dc.contributor.otherChristian Medical College, Velloreen_US
dc.contributor.otherKailashi Superspeciality Hospitalen_US
dc.contributor.otherYangon GI & Liver Centreen_US
dc.contributor.otherSime Darby Medical Centreen_US
dc.contributor.otherSurat Institute of Digestive Sciencesen_US
dc.contributor.otherGlobal Hospital Superspeciality and Transplant Centeren_US
dc.contributor.otherHospital Raja Perempuan Zainab IIen_US
dc.contributor.otherLakeshore Hospitalen_US
dc.contributor.otherHospital Ampangen_US
dc.contributor.otherArtemis Health Instituteen_US
dc.contributor.otherHospital Selayangen_US
dc.contributor.otherHospital Tengku Ampuan Afzanen_US
dc.date.accessioned2019-08-23T11:16:26Z
dc.date.available2019-08-23T11:16:26Z
dc.date.issued2018-12-01en_US
dc.description.abstract© 2018 John Wiley & Sons Ltd There is a paucity of information on chronic hepatitis C (CHC) patients treated with direct antiviral agents (DAAs) in Asia. We invited Asia-Pacific physicians to collate databases of patients enrolled for CHC treatment, recording baseline clinical, virologic and biochemical characteristics, sustained virologic response at week 12 (SVR12) and virologic failure. SVR12 outcome was based on intention to treat (ITT). Multivariate analysis was used to assess independent risk factors for SVR12 using SPSS version 20. A total of 2171 patients from India (n = 977), Myanmar (n = 552), Pakistan (n = 406), Thailand (n = 139), Singapore (n = 72) and Malaysia (n = 25) were collected. At baseline, mean age was 49 years, 50.2% were males, and 41.8% had cirrhosis. Overall, SVR12 was 89.5% and by genotype (GT) based on ITT and treatment completion, respectively, was 91% and 92% for GT1, 100% and 100% for GT2, 91% and 97% for GT3, 64% and 95% for GT4, 87% and 87% for GT6 and 79% and 91% for GT untested. Patients with cirrhosis had SVR12 of 85% vs 93% for noncirrhosis (P < 0.001) (RR 2.1, 95% CI 1.4-3.1, P = 0.0002). Patients with GT1 and GT3 treated with sofosbuvir/ribavirin (SR) had 88% and 89% SVR12, respectively, but those GT6 treated with sofosbuvir/ledipasvir (SL) had only 77.6% SVR12. Multivariate analysis showed absence of cirrhosis was associated with higher SVR12 (OR 2.0, 95% CI 1.3-3.1, P = 0.002). In conclusion, patients with GT1 and GT3 with/without cirrhosis had surprisingly high efficacy using SR, suggesting that Asians may respond better to some DAAs. However, poor GT6 response to SL suggests this regimen is suboptimal for this genotype.en_US
dc.identifier.citationJournal of Viral Hepatitis. Vol.25, No.12 (2018), 1533-1542en_US
dc.identifier.doi10.1111/jvh.12989en_US
dc.identifier.issn13652893en_US
dc.identifier.issn13520504en_US
dc.identifier.other2-s2.0-85053917606en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/45941
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85053917606&origin=inwarden_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titleFindings from a large Asian chronic hepatitis C real-life studyen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85053917606&origin=inwarden_US

Files

Collections