Evidence map›Paper›PMID 19475333›Full record

Trial reportJournal of gastroenterology2009

Lamivudine-to-entecavir switching treatment in type B chronic hepatitis patients without evidence of lamivudine resistance.

Nao Kurashige, Kazuyoshi Ohkawa, Naoki Hiramatsu, Takayuki Yakushijin, Kiyoshi Mochizuki, Tsugiko Oze, Shinichi Kiso, Tatsuya Kanto, Tetsuo Takehara, Akinori Kasahara and 12 more

Abstract readClinical TrialMulticenter Study
PubMed Publisher
In one paragraph

Trial report in Journal of gastroenterology, 2009. 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
1.7field-weighted citation impact, top 16% 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, 13 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

22 authors at 10 institutions in 1 country.

Nao KurashigeDepartment of Gastroenterology and Hepatology, Osaka University Graduate School of Medicine, Suita, Japan.
Kazuyoshi Ohkawa
Naoki Hiramatsu
Takayuki Yakushijin
Kiyoshi Mochizuki
Tsugiko Oze
Shinichi Kiso
Tatsuya Kanto
Tetsuo Takehara
Akinori Kasahara
Yoshinori Doi
Akira Yamada
Kazuto Fukuda
Masahide Oshita
Eiji Mita
Hiroyuki Fukui
Toshihiko Nagase
Harumasa Yoshihara
Yasuharu Imai
Michio Kato
Takeshi Kashihara
Norio Hayashi
Osaka University · JPIkeda Municipal Hospital · JPItami City Hospital · JPNagasaki Rousai Hospital · JPNational Hospital Organization · JPOsaka National Hospital · JPOsaka Police Hospital · JPOtemae Hospital · JPSuita Municipal Hospital · JPSumitomo Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeA considerable number of chronic hepatitis B (CH-B) patients remain under continuous lamivudine treatment, although switching treatment to entecavir could be beneficial. We investigated the antiviral efficacy of switching treatment to entecavir in CH-B patients without apparent evidence of lamivudine resistance during the preceding lamivudine treatment.

methodsForty-four CH-B patients, who underwent lamivudine treatment for more than 6 months and showed no evidence of lamivudine resistance, switched to entecavir. Serial changes in hepatitis B virus (HBV) DNA were correlated with the patients' baseline HBV DNA at the commencement of entecavir administration. The entecavir-resistant substitution was examined by PCR-direct sequencing. The median follow-up period of entecavir treatment was 20 (10-23) months.

resultsAll 31 patients with baseline HBV DNA <2.6 logcopies/ml maintained HBV DNA-negative status during entecavir treatment. Of seven patients having HBV DNA of 2.6-<4.0 logcopies/ml, all achieved undetectable HBV DNA at the end of follow-up. As for six patients having HBV DNA >or=4.0 logcopies/ml, three patients achieved undetectable HBV DNA, whereas virological breakthrough was observed in one patient at month 15. An entecavir-resistant virus having rtM204V, rtL180M and rtS202G substitutions was detected in this patient.

conclusionsThe lamivudine-to-entecavir switching treatment may be generally recommendable in CH-B patients without evidence of lamivudine resistance during the preceding lamivudine treatment. However, great care should be taken with respect to the emergence of entecavir-resistance, especially in patients who do not respond well to the preceding lamivudine treatment.

Indexed as

AdultAgedAntiviral AgentsDNA, ViralDrug Resistance, ViralFemaleFollow-Up StudiesGuanineHepatitis B, ChronicHepatitis B virusHumansLamivudineMaleMiddle AgedPolymerase Chain ReactionSequence Analysis, DNAAntiviral AgentsDNA, ViralentecavirGuanineLamivudine

Identifiers

PMID19475333
OpenAlexW1985418795

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

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.