Literature DB >> 30552159

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

Michele Merli1, Marco Frigeni2, Laurent Alric3, Carlo Visco4, Caroline Besson5, Lara Mannelli6, Alice Di Rocco7, Angela Ferrari8, Lucia Farina9, Mario Pirisi10, Francesco Piazza11, Véronique Loustaud-Ratti12, Annalisa Arcari13, Dario Marino14, Antonello Sica15, Maria Goldaniga16, Chiara Rusconi17, Massimo Gentile18, Emanuele Cencini19, Francesco Benanti20, Maria Grazia Rumi21, Virginia Valeria Ferretti2, Paolo Grossi22, Manuel Gotti23, Roberta Sciarra23, Maria Chiara Tisi4, Isabel Cano24, Valentina Zuccaro25, Francesco Passamonti26, Luca Arcaini2,23.   

Abstract

BACKGROUND: International 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 METHODS: We 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 [ConC]: n = 9) or subsequently (sequential cohort [SeqC]: n = 38) to first-line I-CT (mainly rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone [R-CHOP]-like).
RESULTS: Median 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 (n = 45). Overall, 45 patients (96%) achieved sustained virological response, 8 of 9 in ConC and 37 of 38 in SeqC. DAAs were well tolerated, with only 11 patients experiencing grade 1-2 adverse events. Twenty-three patients experienced hepatic toxicity (grade 3-4 in seven) following I-CT in SeqC, compared to only one patient in ConC. At a median follow-up of 2.8 years, two patients died (2-year overall survival, 97.4%) and three progressed (2-year progression-free survival, 93.1%).
CONCLUSION: Excellent 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. © AlphaMed Press 2018.

Entities:  

Keywords:  Diffuse large B‐cell lymphoma; Direct‐acting antivirals; Hepatitis C virus; R‐CHOP

Year:  2018        PMID: 30552159      PMCID: PMC6693710          DOI: 10.1634/theoncologist.2018-0331

Source DB:  PubMed          Journal:  Oncologist        ISSN: 1083-7159


  31 in total

1.  Antiviral therapy after complete response to chemotherapy could be efficacious in HCV-positive non-Hodgkin's lymphoma.

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2.  Bayesian models identify specific lymphoproliferative disorders associated with hepatitis C virus infection.

Authors:  Luca Arcaini; Cristiana Pascutto; Francesco Passamonti; Raffaele Bruno; Michele Merli; Silvia Rizzi; Ester Orlandi; Cesare Astori; Sara Rattotti; Marco Paulli; Mario Lazzarino
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3.  Characteristics and outcome of diffuse large B-cell lymphoma in hepatitis C virus-positive patients in LNH 93 and LNH 98 Groupe d'Etude des Lymphomes de l'Adulte programs.

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6.  Hepatitis C virus and B-cell non-Hodgkin lymphomas: an Italian multicenter case-control study.

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8.  Impact of treatment-related liver toxicity on the outcome of HCV-positive non-Hodgkin's lymphomas.

Authors:  Luca Arcaini; Michele Merli; Francesco Passamonti; Raffaele Bruno; Ercole Brusamolino; Paolo Sacchi; Sara Rattotti; Ester Orlandi; Elisa Rumi; Virginia Ferretti; Silvia Rizzi; Erika Meli; Cristiana Pascutto; Marco Paulli; Mario Lazzarino
Journal:  Am J Hematol       Date:  2010-01       Impact factor: 10.047

9.  Hepatitis C and non-Hodgkin lymphoma among 4784 cases and 6269 controls from the International Lymphoma Epidemiology Consortium.

Authors:  Silvia de Sanjose; Yolanda Benavente; Claire M Vajdic; Eric A Engels; Lindsay M Morton; Paige M Bracci; John J Spinelli; Tongzhang Zheng; Yawei Zhang; Silvia Franceschi; Renato Talamini; Elizabeth A Holly; Andrew E Grulich; James R Cerhan; Patricia Hartge; Wendy Cozen; Paolo Boffetta; Paul Brennan; Marc Maynadié; Pierluigi Cocco; Ramon Bosch; Lenka Foretova; Anthony Staines; Nikolaus Becker; Alexandra Nieters
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2.  Cancer in People with and without Hepatitis C Virus Infection: Comparison of Risk Before and After Introduction of Direct-Acting Antivirals.

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4.  Cancer- and Non-cancer Related Chronic Pain: From the Physiopathological Basics to Management.

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6.  Endoscopic Treatment and Pulmonary Rehabilitation for Management of Lung Abscess in Elderly Lymphoma Patients.

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