Evidence map›Paper›PMID 28939993›Full record

Trial reportAnnals of hematology2017

Efficacy and prognosis of antiviral therapy on hepatitis C following treatment of lymphoma in HCV-positive diffuse large-cell lymphoma.

Yutaka Tsutsumi, Chie Nakayama, Koki Kamada, Ryo Kikuchi, Daiki Kudo, Shinichi Ito, Satomi Matsuoka, Souichi Shiratori, Yoshiya Yamamoto, Hirohito Naruse and 1 more

Open access · hybridAbstract readClinical Trial
In one paragraph

Trial report in Annals of hematology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

6 citing papers in PubMed, 15 citations in OpenAlex.

  1. Viral oncogenesis in cancer: from mechanisms to therapeutics.Signal transduction and targeted therapy · 2025
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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

11 authors at 1 institution in 1 country.

Yutaka TsutsumiDepartment of Hematology, Hakodate Municipal Hospital 1-10-1, Minato-Cho, Hakodate, 041-8680, Japan. yutsutsu@shore.ocn.ne.jp.
Chie NakayamaDepartment of Hematology, Hakodate Municipal Hospital 1-10-1, Minato-Cho, Hakodate, 041-8680, Japan.
Koki KamadaDepartment of Hematology, Hakodate Municipal Hospital 1-10-1, Minato-Cho, Hakodate, 041-8680, Japan.
Ryo KikuchiDepartment of Hematology, Hakodate Municipal Hospital 1-10-1, Minato-Cho, Hakodate, 041-8680, Japan.
Daiki KudoDepartment of Gastroenterology, Hakodate Municipal Hospital, Hakodate, Japan.
Shinichi ItoDepartment of Hematology, Hakodate Municipal Hospital 1-10-1, Minato-Cho, Hakodate, 041-8680, Japan.
Satomi MatsuokaDepartment of Hematology, Hakodate Municipal Hospital 1-10-1, Minato-Cho, Hakodate, 041-8680, Japan.
Souichi ShiratoriDepartment of Hematology, Hokkaido Graduate School of Medicine, Sapporo, Japan.
Yoshiya YamamotoDepartment of Gastroenterology, Hakodate Municipal Hospital, Hakodate, Japan.
Hirohito NaruseDepartment of Gastroenterology, Hakodate Municipal Hospital, Hakodate, Japan.
Takanori TeshimaDepartment of Hematology, Hokkaido Graduate School of Medicine, Sapporo, Japan.
Hakodate National Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The purpose of this study is to study the usefulness of post-remission antiviral therapy in cases of HCV-RNA-positive diffuse large-cell lymphoma. Antiviral therapy against HCV was performed after remission using CHOP or CHOP-like chemotherapy in combination with rituximab in five successive cases of HCV-RNA-positive diffuse large-cell lymphoma. The control groups consisted of a group of HCV-RNA-positive diffuse large-cell lymphoma cases prior to this trial (control 1), and a group of cases that tested negative for HIV, HCV, and HBV (control 2). All the cases were in remission at the time of initial treatment. There were no significant differences between the three groups in terms of age, sex, treatment, stage, or International Prognosis Index (IPI). When HCV antiviral therapy was performed after treatment for diffuse large-cell lymphoma, we observed no recurrence or deaths, and the 2-year overall survival and progression-free survival rates were significantly greater than those in the control 1 group (P = 0.0246). It is possible that a better prognosis can be achieved by performing HCV antiviral therapy after achieving remission in cases of HCV-RNA-positive diffuse large-cell lymphoma through the use of R-CHOP or similar treatments.

Indexed as

Hepatitis CLymphoma, Large B-Cell, DiffuseAdultAgedAged, 80 and overAntibodies, Monoclonal, Murine-DerivedAntineoplastic Combined Chemotherapy ProtocolsAntiviral AgentsCyclophosphamideDisease-Free SurvivalDoxorubicinFemaleHepacivirusHumansMaleMiddle AgedAntibodies, Monoclonal, Murine-DerivedAntiviral AgentsCyclophosphamideDoxorubicinPrednisoneR-CHOP protocolRituximabRNA, ViralVincristineDiffuse large B cell lymphoma (DLBCL)Direct-acting antiviral agents (DAAs)HCV

Identifiers

PMID28939993
PMCPMC5691112
OpenAlexW2758351365

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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.