Evidence map›Paper›PMID 26202029›Full record

ArticleHepatology international2013

The virological response in Koreans infected with HCV genotype 1 did not differ between groups treated with a full dose or reduced dose (≥80 % full dose) of peginterferon alfa-2a: a prospective randomized multicenter trial.

Jung Hyun Kwon, Si Hyun Bae, Youn Jae Lee, Jin-Woo Lee, Young Seok Kim, Jae Seok Hwang, Won Young Tak, Jeong Won Jang, Byung Seok Lee, June Sung Lee and 8 more

Abstract read
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In one paragraph

Article in Hepatology international, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 46% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors at 14 institutions in 1 country.

Jung Hyun KwonDepartment of Internal Medicine, Incheon St. Mary's Hospital, The Catholic University of Korea, Incheon, Korea. doctorkwon@catholic.ac.kr.
Si Hyun BaeDepartment of Internal Medicine, Seoul St. Mary's Hospital, The Catholic University of Korea, 505 Banpo-dong, Seocho-gu, Seoul, 137-040, Korea. baesh@catholic.ac.kr.
Youn Jae LeeDepartment of Internal Medicine, Pusan Paik Hospital, Inje University of Korea, Gaegum-dong 633-165, Busanjin-gu, Pusan, 614-735, Korea. yiyh0105@inje.ac.kr.
Jin-Woo LeeDepartment of Internal Medicine, Inha University School of Medicine, Incheon, Korea. jin@inha.ac.kr.
Young Seok KimDepartment of Internal Medicine, Bucheon Soonchunhyang Hospital, Soonchunhyang University of Korea, Bucheon, Korea. liverkys@schmc.ac.kr.
Jae Seok HwangDepartment of Internal Medicine, Dongsan Hospital, Keimyung University of Korea, Taegu, Korea. gastro@dsmc.or.kr.
Won Young TakDepartment of Internal Medicine, Kyungpook National University Hospital, Kyungpook National University of Korea, Taegu, Korea. wytak@knu.ac.kr.
Jeong Won JangDepartment of Internal Medicine, Seoul St. Mary's Hospital, The Catholic University of Korea, 505 Banpo-dong, Seocho-gu, Seoul, 137-040, Korea. garden@catholic.ac.kr.
Byung Seok LeeDepartment of Internal Medicine, Chungnam National University Hospital, Chungnam National University of Korea, Taejon, Korea. gie001@cnuh.co.kr.
June Sung LeeDepartment of Internal Medicine, Ilsan Paik Hospital, Inje University of Korea, Ilsan, Korea. jsleemd@paik.ac.kr.
Chun Kyon LeeDepartment of Internal Medicine, National Health Insurance Corporation Ilsan Hospital, Ilsan, Korea. cklee33@nhimc.or.kr.
Soon Koo BaikDepartment of Internal Medicine, Wonju Christian Hospital, Yonsei University of Korea, Wonju, Korea. baiksk@yonsei.ac.kr.
Neung Hwa ParkDepartment of Internal Medicine, Ulsan University Hospital, Ulsan University of Korea, Ulsan, Korea. nhpark@uuh.ulsan.kr.
Tae Hee LeeDepartment of Internal Medicine, Konyang University Hospital, Konyang University of Korea, Taejon, Korea. green740@naver.com.
Dong Joon KimDepartment of Internal Medicine, Chuncheon Sacred Heart Hospital, Hallym University of Korea, Chuncheon, Korea. djkim@hallym.ac.kr.
Jae-Seok ChoiDepartment of Pharmacology and PharmacoGenomics Research Center, Inje University of Korea, Pusan, Korea. karis@hanmail.net.
Jae-Gook ShinDepartment of Pharmacology and PharmacoGenomics Research Center, Inje University of Korea, Pusan, Korea. phshinjg@gmail.com.
Hyeon Woo YimClinical Research Coordinating Center for Catholic Medical Center, The Catholic University of Korea, Seoul, Korea. y1693@catholic.ac.kr.
Inje University · KRCatholic University of Korea · KRChungnam National University Hospital · KRHallym University · KRInha University · KRKeimyung University · KRKonyang University Hospital · KRKyungpook National University Hospital · KRNational Health Insurance Service Ilsan Hospital · KRSoonchunhyang University · KRThe Catholic University of Korea Incheon St. Mary's Hospital · KRThe Catholic University of Korea Seoul St. Mary's Hospital · KRUlsan University Hospital · KRWonju Severance Christian Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeA high rate of sustained viral response (SVR) in Koreans with chronic hepatitis C (CHC) is related to a favorable IL28B genotype. We compared two dosing strategies for peginterferon alfa-2a in Koreans with CHC and defined the combined effect of polymorphisms and dosing on the virological response.

methodsA total of 178 treatment-naïve patients with CHC genotype 1 were prospectively enrolled. All patients were randomly assigned to treatment with one of two peginterferon alfa-2a regimens: 180 μg per week for 48 weeks (full-dose group) or 180 μg per week during the first 12 weeks followed by 135 μg per week for the next 36 weeks (dose-reduction group). Polymorphisms related to IL28B, ITPA, C20orf194 and SLC29A1 were studied.

resultsSVR rates did not differ between the full-dose and dose-reduction groups (56.5 and 51.2 %, respectively, p = 0.474). The frequency of additional reductions of the peginterferon dose because of adverse events was higher in the full-dose group than in the dose-reduction group. SVR rates in patients homozygous for the IL28B major allele were higher than those in patients for the other IL28B alleles. For patients with unfavorable IL28B genotypes, SVR was less likely to be achieved in the dose-reduction group than in the full-dose group.

conclusionsIn Koreans with HCV genotype 1, the virological response to treatment did not differ between a full dose and reduced dose (≥80 % of full dose) of peginterferon alfa-2a. However, in the patients with unfavorable IL28B genotypes, the full-dose treatment of peginterferon alfa-2a may be beneficial.

Indexed as

Chronic hepatitis CGenotype 1IL28BInterferon dosingPolymorphism

Identifiers

PMID26202029
OpenAlexW1999063732

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.