Concomitant therapy with direct-acting antivirals and chemoimmunotherapy in HCV-associated diffuse large B-cell lymphoma

被引:11
作者
Occhipinti, Vincenzo [1 ]
Farina, Lucia [2 ]
Vigano, Mauro [1 ]
Capecchi, Marco [2 ]
Labanca, Sara [1 ]
Fanetti, Ilaria [1 ]
Corradini, Paolo [2 ]
Rumi, Mariagrazia [1 ]
机构
[1] Univ Milan, Hepatol Unit, San Giuseppe Hosp, Via San Vittore 12, I-20123 Milan, Italy
[2] Fdn IRCCS Ist Nazl Tumori, Dept Hematol, Milan, Italy
关键词
Chemoimmunotherapy; Diffuse large B-cell lymphoma; Direct-acting antivirals; Hepatitis C virus; Rituximab; Safety; HEPATITIS-C-VIRUS; MARGINAL ZONE LYMPHOMA; NON-HODGKIN LYMPHOMAS; INTERFERON-FREE; INFECTION; TOXICITY; REACTIVATION; REGRESSION; IMPACT; RISK;
D O I
10.1016/j.dld.2018.10.019
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Introduction: The association between hepatitis C virus (HCV) infection and B-cell non-Hodgkin's Lymphomas (NHL) is well established. Antiviral therapy (AVT) is the first-line treatment for HCV-related indolent NHL whereas diffuse large B-cell lymphoma (DLBCL) requires immediate start of chemoimmunotherapy (CIT), usually deferring AVT. However, an early HCV elimination may reduce the risk of CIT-induced liver toxicity and consequent CIT interruption or withdrawal. To date few data are available on safety and efficacy of concomitant administration of direct-acting antivirals (DAA) and CIT in HCV-associated DLBCL. Methods: 7 consecutive patients (5 males, median age 65 years) with HCV infection (four genotype 2a/2c, two genotype 1b, one genotype 4; one patient with compensated cirrhosis) and DLBCL received different DAA regimens concurrently with CIT. Results: All patients completed the scheduled AVT and CIT with neither interruption nor withdrawal of the latter. One case of neutropenia was observed during concomitant therapy, no liver toxicity occurred. All patients achieved sustained virological response and complete DLBCL response (median follow-up of 12 months). Conclusions: Concomitant administration of DAA and CIT for HCV-associated DLBCL is safe and may prevent CIT-induced liver toxicity. Large, prospective studies are needed to confirm these preliminary data and to assess prognostic implications. (C) 2018 Editrice Gastroenterologica Italiana S.r.l. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:719 / 723
页数:5
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