Evidence map›Paper›PMID 30552159›Full record

ArticleThe oncologist2019

Direct-Acting Antivirals in Hepatitis C Virus-Associated Diffuse Large B-cell Lymphomas.

Michele Merli, Marco Frigeni, Laurent Alric, Carlo Visco, Caroline Besson, Lara Mannelli, Alice Di Rocco, Angela Ferrari, Lucia Farina, Mario Pirisi and 20 more

Open access · bronzeAbstract readMulticenter Study
In one paragraph

Article in The oncologist, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
6.3field-weighted citation impact, top 2% 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

34 citing papers in PubMed, 67 citations in OpenAlex.

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  10. [Evolution of clinical outcomes following hepatitis C virus clearance].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2022
    Article
  11. Review
  12. Cancer in People with and without Hepatitis C Virus Infection: Comparison of Risk Before and After Introduction of Direct-Acting Antivirals.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2021
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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

30 authors at 20 institutions in 2 countries.

Michele MerliHematology, University Hospital Ospedale di Circolo e Fondazione Macchi-ASST Sette Laghi, University of Insubria, Varese, Italy michele.merli@asst-settelaghi.it.ORCID 0000-0002-0905-5927
Marco FrigeniDepartment of Molecular Medicine, University of Pavia, Pavia, Italy.
Laurent AlricDepartment of Internal Medicine and Digestive Diseases, University Hospital Toulouse, UMR 152 PharmaDev, IRD Toulouse 3 University, France.
Carlo ViscoCell Therapy and Hematology, Ospedale San Bortolo, Vicenza, Italy.
Caroline BessonUnit of Hematology-Oncology, Centre Hospitalier de Versailles, Le Chesnay; Université Versailles Saint Quentin en Yvelines; INSERM U1018, Centre pour la Recherche en Epidemiologie et Sante des Populations (CESP), Equipe Generations et Sante, Gustave Roussy, Villejuif, France.
Lara MannelliHematology, Azienda Ospedaliera Careggi, Florence, Italy.
Alice Di RoccoCellular Biotechnologies and Hematology, Sapienza University of Rome, Rome, Italy.
Angela FerrariHematology Unit, Azienda Unità Sanitaria Locale-IRCCS Reggio Emilia, Italy.
Lucia FarinaHematology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Mario PirisiTranslational Medicine, University of Piemonte Orientale UPO, Novara, Italy.
Francesco PiazzaMedicine-Hematology, University of Padova, Padova, Italy.
Véronique Loustaud-RattiHepatology, Centre Hospitalier Universitaire de Limoges, U-1248 INSERM, Université de Limoges, Limoges, France.
Annalisa ArcariHaematology Unit, Azienda AUSL, Piacenza, Italy.
Dario MarinoDepartment of Clinical and Experimental Oncology, Veneto Institute of Oncology, IOV IRCCS, Padova, Italy.
Antonello SicaOncology and Hematology, AOU "Luigi Vanvitelli", Naples, Italy.
Maria GoldanigaHematology, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Chiara RusconiHematology and Oncology, Niguarda Cancer Center, Ospedale Niguarda Ca' Granda, Milan, Italy.
Massimo GentileOnco-Hematology, Hematology Unit, AO of Cosenza, Cosenza, Italy.
Emanuele CenciniHematology, Azienda Ospedaliera Senese, University of Siena, Siena, Italy.
Francesco BenantiInfectious Diseases, University of Catania, Catania, Italy.
Maria Grazia RumiHepatology, Ospedale San Giuseppe IRCCS Multimedica, University of Milan, Milan, Italy.
Virginia Valeria FerrettiDepartment of Molecular Medicine, University of Pavia, Pavia, Italy.
Paolo GrossiInfectious and Tropical Diseases, University Hospital Ospedale di Circolo e Fondazione Macchi - ASST Sette Laghi, University of Insubria, Varese, Italy.
Manuel GottiDivision of Hematology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Roberta SciarraDivision of Hematology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
Maria Chiara TisiCell Therapy and Hematology, Ospedale San Bortolo, Vicenza, Italy.
Isabel CanoHematology Department, Centre Hospitalier de Versailles, Versailles, France.
Valentina ZuccaroInfectious and Tropical Diseases, Fondazione IRCCS Policlinico San Matteo, University of Pavia, Pavia, Italy.
Francesco PassamontiHematology, University Hospital Ospedale di Circolo e Fondazione Macchi-ASST Sette Laghi, University of Insubria, Varese, Italy.
Luca ArcainiDepartment of Molecular Medicine, University of Pavia, Pavia, Italy.
Istituti di Ricovero e Cura a Carattere Scientifico · ITUniversity of Pavia · ITOspedale di Circolo e Fondazione Macchi · ITOspedale San Bortolo · ITAzienda Ospedaliera di Cosenza · ITAzienda Ospedaliero-Universitaria Careggi · ITAzienda Sanitaria Unità Locale di Reggio Emilia · ITAzienda Socio Sanitaria Territoriale Grande Ospedale Metropolitano Niguarda · ITAzienda Unità Sanitaria Locale Piacenza · ITCentre de recherche en Epidémiologie et Santé des Populations · FRCentre Hospitalier de Versailles · FRFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · ITFondazione IRCCS Istituto Nazionale dei Tumori · ITInstitut de Recherche pour le Développement · FROspedale San Giuseppe · ITSapienza University of Rome · ITUniversità degli Studi del Piemonte Orientale “Amedeo Avogadro” · ITUniversité de Limoges · FRUniversity of Campania "Luigi Vanvitelli" · ITUniversity of Catania · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInternational guidelines suggest hepatitis C virus (HCV) eradication by direct-acting antivirals (DAAs) after first-line immunochemotherapy (I-CT) in patients with HCV-positive diffuse large B-cell lymphoma (DLBCL), although limited experiences substantiate this recommendation. Moreover, only a few data concerning concurrent administration of DAAs with I-CT have been reported. SUBJECTS, MATERIALS, AND

methodsWe analyzed hematological and virological outcome and survival of 47 consecutive patients with HCV-positive DLBCL treated at 23 Italian and French centers with DAAs either concurrently (concurrent cohort [

resultsMedian age was 61 years, 89% of patients had stage III/IV, and 25% presented evidence of cirrhosis. Genotype was 1 in 56% and 2 in 34% of cases. Overall, 46 of 47 patients obtained complete response to I-CT. All patients received appropriate DAAs according to genotype, mainly sofosbuvir-based regimens (

conclusionExcellent outcome of this cohort of HCV-positive DLBCL suggests benefit of HCV eradication by DAAs either after or during I-CT. Moreover, concurrent DAAs and R-CHOP administration appeared feasible, effective, and ideally preferable to deferred administration of DAAs for the prevention of hepatic toxicity. IMPLICATIONS FOR PRACTICE: Hepatitis C virus (HCV)-associated diffuse large B-cell lymphomas (DLBCLs) represent a great therapeutic challenge, especially in terms of hepatic toxicity during immune-chemotherapy (I-CT) and long-term hepatic complications. The advent of highly effective and toxicity-free direct-acting antivirals (DAAs) created an exciting opportunity to easily eradicate HCV shortly after or in concomitance with first-line immunochemotherapy (usually R-CHOP). This retrospective international study reports the real-life use of the combination of these two therapeutic modalities either in the concurrent or sequential approach (DAAs after I-CT) in 47 patients. The favorable reported results on long-term outcome seem to support the eradication of HCV with DAAs in all patients with HCV-positive DLBCL. Moreover, the results from the concurrent approach were effective and safe and displayed an advantage in preventing hepatic toxicity during I-CT.

Indexed as

AdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsAntiviral AgentsCyclophosphamideDisease-Free SurvivalDoxorubicinFemaleHepacivirusHepatitis C, ChronicHumansIncidenceItalyLymphoma, Large B-Cell, DiffuseMaleAntiviral AgentsCyclophosphamideDoxorubicinPrednisoneRituximabVincristineDiffuse large B‐cell lymphomaDirect‐acting antiviralsHepatitis C virusR‐CHOP

Identifiers

PMID30552159
PMCPMC6693710
OpenAlexW2904829109

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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.