TY - JOUR
T1 - Findings from a large Asian chronic hepatitis C real-life study
AU - Lim, Seng Gee
AU - Phyo, Wah Wah
AU - Shah, Samir R.
AU - Win, Khin Maung
AU - Hamid, Saeed
AU - Piratvisuth, Teerha
AU - Tan, Soek Siam
AU - Dan, Yock Young
AU - Lee, Yin Mei
AU - Ahmed, Taufique
AU - Yang, Wei Lyn
AU - Chen, Kok Pun
AU - Kamat, Mrunal
AU - Wadhawan, Manav
AU - Madan, Kaushal
AU - Mehta, Rajiv
AU - Shukla, Akash
AU - Dhore, Prashant
AU - Eapen, Chundamannil E.
AU - Abraham, Priya
AU - Tyagi, Satyendra
AU - Koshy, Abraham
AU - Bwa, Aung Hlaing
AU - Jafri, Wasim
AU - Abid, Shahab
AU - Arisar, Fakhar Ali Qazi
AU - Tanwandee, Tewesak
AU - Yin, Thing Phee
AU - Tee, Hoi Poh
AU - Hj Md Said, Rosaida Binti
AU - Goh, Khean Lee
AU - Ho, Shiaw Hooi
AU - Mohamed, Rosmawati
AU - Abu Bakar, Norasiah
N1 - Funding Information:
Seng Gee Lim was a member of the Advisory Board for Gilead Sciences, Merck Sharpe and Dohme, AbbVie, Abbott; was on the Speakers’ Bureau for Gilead, AbbVie, Abbott; and has received educational/research funding from Merck Sharpe and Dohme, Gilead Sciences. Wah Wah Phyo, Khin Maung Win, Saeed Hamid, Yin Mei Lee, Kok Pun Chen, Mrunal Kamat, Manav Wadhwan, Rajiv Mehta, Akash Shukla, Prashant Dhore, C.E. Eapen, Satyendra Tyagi, Wasim Jafri, Shahab Abid, Fakhar Ali ?azi Arisar, Aung Hlaing Bwa, Yin Thing Phee, Rosaida Binti Hj Md Said, Shiaw Hooi Ho, Norasiah Abu Bakar declared no conflict of interests. Samir R. Shah was a member of Advisory Board/Speaker for Mylan, Biocon, Emcure, Natco, Cipla and has received research grants from Gilead. Teerha Piratvisuth was a member of Advisory Board for Novartis, Merck Sharpe and Dohme, Roche; was on the Speakers’ Bureau for GlaxoSmithKline, Bristol Myers Squibb, Novartis, Merck Sharpe and Dohme, Roche; and has received educational/research funding from Novartis, Roche, Bristol Myers Squibb. Soek Siam Tan was a member of Advisory Board for AbbVie. Yock Young Dan was a member of Advisory Board for Merck Sharpe and Dohme, Gilead Sciences, Bristol Myers Squibb, Novartis. Taufique Ahmed was a member of Advisory Board for Gilead. Wei Lyn Yang was a member of Advisory board for Gilead, MSD, AbbVie, BMS. Kaushal Madan was a member of Advisory boards or was a Speaker at meetings for Gilead Sciences, Mylan, Cipla, Dr Reddy’s Labs, Abbott, Zydus, Biocon, Hetero. Priya Abraham was a Speaker for Abbott Diagnostics, Ortho Diagnostic systems. Abraham Koshy was a member of Advisory Board for Torrent; was on the Speaker’s Bureau for Mylan, Cipla; and has received educational/research funding from Dr. Reddy. Tewesak Tanwandee has received educational/research funding from Merck Sharpe and Dohme, Bristol Myer Squibb, Novartis, Biotron, Roche. Tee Hoi Poh was a member of Advisory Board for AbbVie, MSD. Khean Lee Goh was a member of Advisory Board for Gilead Sciences, AbbVie (Malaysia) and was on the Speakers’ Bureau for AbbVie Malaysia, Roche Malaysia. Rosmawati Mohamed was a member of Advisory Board for Gilead Sciences, Merck Sharpe and Dohme, Abbott and was on the Speakers’ Bureau for Merck Sharpe and Dohme, Abbott.
Publisher Copyright:
© 2018 John Wiley & Sons Ltd
PY - 2018/12
Y1 - 2018/12
N2 - 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.
AB - 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.
KW - chronic hepatitis C
KW - cure
KW - genotype
KW - sustained virologic response
KW - treatment failure
KW - virologic failure
UR - http://www.scopus.com/inward/record.url?scp=85053917606&partnerID=8YFLogxK
U2 - 10.1111/jvh.12989
DO - 10.1111/jvh.12989
M3 - Article
C2 - 30141214
AN - SCOPUS:85053917606
SN - 1352-0504
VL - 25
SP - 1533
EP - 1542
JO - Journal of Viral Hepatitis
JF - Journal of Viral Hepatitis
IS - 12
ER -