Biological features and outcome of diffuse large B‐cell lymphoma associated with hepatitis C virus in elderly patients: Results of the prospective ‘Elderly Project’ by the Fondazione Italiana Linfomi

医学 内科学 长春新碱 弥漫性大B细胞淋巴瘤 丙型肝炎病毒 美罗华 强的松 淋巴瘤 胃肠病学 丙型肝炎 环磷酰胺 免疫学 化疗 病毒
作者
Annalisa Arcari,Valentina Tabanelli,Francesco Merli,Luigi Marcheselli,Michele Merli,Monica Balzarotti,Vittorio Ruggero Zilioli,Alberto Fabbri,Federica Cavallo,Gloria Margiotta Casaluci,Alessandra Tucci,Benedetta Puccini,Elsa Pennese,Alice Di Rocco,Manuela Zanni,Leonardo Flenghi,Guido Gini,Roberto Sartori,Annalisa Chiappella,Sara Veronica Usai,Monica Tani,Dario Marino,Luca Arcaini,Daniele Vallisa,Michele Spina
出处
期刊:British Journal of Haematology [Wiley]
卷期号:201 (4): 653-662 被引量:4
标识
DOI:10.1111/bjh.18678
摘要

Up to 10%-15% of diffuse large B-cell lymphoma (DLBCL) are related to hepatitis C virus (HCV) infection, in particular in elderly patients. The Fondazione Italiana Linfomi has recently published a multicentre prospective observational study, the 'Elderly Project', on the outcome of DLBCL in patients aged ≥65 years, evaluated using a simplified comprehensive geriatric assessment. The aim of this study was to compare biological and clinical features of HCV positive (HCV+) with HCV negative (HCV-) cases. A total of 89 HCV+ patients were identified out of 1095 evaluated for HCV serology (8.1%). The HCV+ patients were older, less fit, and had frequent extranodal involvement. The cell-of-origin determination by Nanostring showed that HCV+ cases less frequently had an activated B-cell profile compared to HCV- patients (18% vs. 43%). In all, 86% of HCV+ patients received rituximab-cyclophosphamide, doxorubicin, vincristine (Oncovin) and prednisone (R-CHOP)-like immunochemotherapy. Grade 3-4 liver toxicity occurred in 3% of cases. Among centrally reviewed cases confirmed as DLBCL, the 3-year overall survival of HCV+ patients was very similar to HCV- (63% vs. 61%, p = 0.926). In all, 20 HCV+ patients were treated with direct-acting antiviral agents (DAAs), with good tolerance and sustained virological response in all cases. The 3-year progression-free survival for this subgroup was excellent (77%), suggesting DAAs' possible role in reducing the risk of relapse by eliminating the viral trigger.
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