Evidence map›Paper›PMID 29545925›Full record

ArticleOncotarget2018

Interferon-free treatment for patients with chronic hepatitis C and autoimmune liver disease: higher SVR rates with special precautions for deterioration of autoimmune hepatitis.

Tatsuo Kanda, Shin Yasui, Masato Nakamura, Shingo Nakamoto, Koji Takahashi, Shuang Wu, Reina Sasaki, Yuki Haga, Sadahisa Ogasawara, Tomoko Saito and 9 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Hepatitis C: A Pharmacological Therapeutic Update.Journal of clinical medicine · 2021
    Review
  4. Article
  5. Article
  6. Article
  7. Article
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

19 authors at 2 institutions in 1 country.

Tatsuo KandaDivision of Gastroenterology and Hepatology, Department of Medicine, Nihon University School of Medicine, Tokyo 173-8610, Japan.
Shin YasuiDepartment of Gastroenterology, Chiba University, Graduate School of Medicine, Chiba 260-8670, Japan.
Masato NakamuraDepartment of Gastroenterology, Chiba University, Graduate School of Medicine, Chiba 260-8670, Japan.
Shingo NakamotoDepartment of Gastroenterology, Chiba University, Graduate School of Medicine, Chiba 260-8670, Japan.
Koji TakahashiDepartment of Gastroenterology, Chiba University, Graduate School of Medicine, Chiba 260-8670, Japan.
Shuang WuDepartment of Gastroenterology, Chiba University, Graduate School of Medicine, Chiba 260-8670, Japan.
Reina SasakiDepartment of Gastroenterology, Chiba University, Graduate School of Medicine, Chiba 260-8670, Japan.
Yuki HagaDepartment of Gastroenterology, Chiba University, Graduate School of Medicine, Chiba 260-8670, Japan.
Sadahisa OgasawaraDepartment of Gastroenterology, Chiba University, Graduate School of Medicine, Chiba 260-8670, Japan.
Tomoko SaitoDepartment of Gastroenterology, Chiba University, Graduate School of Medicine, Chiba 260-8670, Japan.
Kazufumi KobayashiDepartment of Gastroenterology, Chiba University, Graduate School of Medicine, Chiba 260-8670, Japan.
Soichiro KiyonoDepartment of Gastroenterology, Chiba University, Graduate School of Medicine, Chiba 260-8670, Japan.
Yoshihiko OokaDepartment of Gastroenterology, Chiba University, Graduate School of Medicine, Chiba 260-8670, Japan.
Eiichiro SuzukiDepartment of Gastroenterology, Chiba University, Graduate School of Medicine, Chiba 260-8670, Japan.
Tetsuhiro ChibaDepartment of Gastroenterology, Chiba University, Graduate School of Medicine, Chiba 260-8670, Japan.
Hitoshi MaruyamaDepartment of Gastroenterology, Chiba University, Graduate School of Medicine, Chiba 260-8670, Japan.
Fumio ImazekiDepartment of Gastroenterology, Chiba University, Graduate School of Medicine, Chiba 260-8670, Japan.
Mitsuhiko MoriyamaDivision of Gastroenterology and Hepatology, Department of Medicine, Nihon University School of Medicine, Tokyo 173-8610, Japan.
Naoya KatoDepartment of Gastroenterology, Chiba University, Graduate School of Medicine, Chiba 260-8670, Japan.
Chiba University · JPNihon University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInterferon-free treatment can achieve higher sustained virological response (SVR) rates, even in patients in whom hepatitis C virus (HCV) could not be eradicated in the interferon treatment era. Immune restoration in the liver is occasionally associated with HCV infection. We examined the safety and effects of interferon-free regimens on HCV patients with autoimmune liver diseases.

resultsAll 7 HCV patients with autoimmune hepatitis (AIH) completed treatment and achieved SVR. Three patients took prednisolone (PSL) at baseline, and 3 did not take PSL during interferon-free treatment. In one HCV patient with AIH and cirrhosis, PSL were not administered at baseline, but she needed to take 40 mg/day PSL at week 8 for liver dysfunction. She also complained back pain and was diagnosed with vasospastic angina by coronary angiography at week 11. However, she completed interferon-free treatment. All 5 HCV patients with primary biliary cholangitis (PBC) completed treatment and achieved SVR. Three of these HCV patients with PBC were treated with UDCA during interferon-free treatment.

conclusionsInterferon-free regimens could result in higher SVR rates in HCV patients with autoimmune liver diseases. As interferon-free treatment for HCV may have an effect on hepatic immunity and activity of the autoimmune liver diseases, careful attention should be paid to unexpected adverse events in their treatments.

methodsTotal 12 patients with HCV and autoimmune liver diseases [7 AIH and PBC], who were treated with interferon-free regimens, were retrospectively analyzed.

Indexed as

autoimmune hepatitisdirect-acting antiviralshepatitis C virusprimary biliary cholangitissustained virological response

Identifiers

PMID29545925
PMCPMC5837765
OpenAlexW2792724662

What OpenQuestion holds

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LicenceCC BY
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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.