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DC Field | Value | Language |
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dc.contributor.author | Phunchai Charatcharoenwitthaya | en_US |
dc.contributor.author | Wattana Sukeepaisarnjaroen | en_US |
dc.contributor.author | Teerha Piratvisuth | en_US |
dc.contributor.author | Satawat Thongsawat | en_US |
dc.contributor.author | Theeranun Sanpajit | en_US |
dc.contributor.author | Soonthorn Chonprasertsuk | en_US |
dc.contributor.author | Woramon Jeamsripong | en_US |
dc.contributor.author | Ekawee Sripariwuth | en_US |
dc.contributor.author | Piyawat Komolmit | en_US |
dc.contributor.author | Tanisa Patcharatrakul | en_US |
dc.contributor.author | Rattana Boonsirichan | en_US |
dc.contributor.author | Chalermrat Bunchorntavakul | en_US |
dc.contributor.author | Supoj Tuntipanichteerakul | en_US |
dc.contributor.author | Tawesak Tanwandee | en_US |
dc.date.accessioned | 2018-09-05T03:08:01Z | - |
dc.date.available | 2018-09-05T03:08:01Z | - |
dc.date.issued | 2016-11-01 | en_US |
dc.identifier.issn | 14401746 | en_US |
dc.identifier.issn | 08159319 | en_US |
dc.identifier.other | 2-s2.0-84996565533 | en_US |
dc.identifier.other | 10.1111/jgh.13378 | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84996565533&origin=inward | en_US |
dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/56029 | - |
dc.description.abstract | © 2016 Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd Background and Aims: Peginterferon has demonstrated effectiveness in clinical trials in patients with chronic hepatitis B (CHB). However, its efficacy in real-life settings remains unclear. We investigated the efficacy of peginterferon for CHB and validated the performance of previously identified response predictors in clinical practice. Methods: We analyzed prospectively collected data from a Thai nationwide cohort of CHB patients treated with peginterferon alfa-2a (180 µg/week, 48 weeks). Results: Among a total of 233 patients, mostly with genotype B or C, sustained response was observed in 23% of 135 hepatitis B e antigen (HBeAg)-positive patients (HBeAg seroconversion with hepatitis B virus [HBV] DNA < 2000 IU/mL) and 42% of 98 HBeAg-negative patients (HBV DNA < 2000 IU/mL with aminotransferase normalization) at 24 weeks after treatment. Age, sex, presence of cirrhosis, genotype, and pretreatment levels of aminotransferase, HBV DNA, and hepatitis B surface antigen (HBsAg) were not identified as significant predictors of sustained response. In HBeAg-positive patients, HBsAg > 20 000 IU/mL at week 12 provided a good stopping rule, with a negative predictive value of 96%. In HBeAg-negative patients, the performance of 12-week stopping rules of no decline in HBsAg with a < 2log10 decline in HBV DNA and a < 10% log10 decline in HBsAg showed modest negative predictive values of 80% and 66%, respectively, for achieving sustained response. Conclusion: Outcomes in CHB patients treated with peginterferon in a clinical setting are similar to those demonstrated in clinical trials. Application of the early stopping rule based on HBsAg quantification may allow individualization of therapy, particularly in HBeAg-positive patients. | en_US |
dc.subject | Medicine | en_US |
dc.title | Treatment outcomes and validation of the stopping rule for response to peginterferon in chronic hepatitis B: A Thai nationwide cohort study | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | Journal of Gastroenterology and Hepatology (Australia) | en_US |
article.volume | 31 | en_US |
article.stream.affiliations | Mahidol University | en_US |
article.stream.affiliations | Khon Kaen University | en_US |
article.stream.affiliations | Prince of Songkla University | en_US |
article.stream.affiliations | Chiang Mai University | en_US |
article.stream.affiliations | Phramongkutklao College of Medicine | en_US |
article.stream.affiliations | Faculty of Medicine, Thammasat University | en_US |
article.stream.affiliations | Buddhachinaraj Hospital | en_US |
article.stream.affiliations | Naresuan University | en_US |
article.stream.affiliations | Chulalongkorn University | en_US |
article.stream.affiliations | Police General Hospital | en_US |
article.stream.affiliations | Vajira Hospital | en_US |
article.stream.affiliations | Rajavithi Hospital | en_US |
article.stream.affiliations | Bhumibol Adulyadej Hospital | en_US |
Appears in Collections: | CMUL: Journal Articles |
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