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

Epidemiologic studies show an association between hepatitis C virus (HCV) and B-cell non-Hodgkin's lymphoma (NHL). Treatment and outcome of patients with diffuse large-cell lymphoma (DLCL) and HCV infection are still a matter of debate. We studied the HCV-positive patients with B-cell DLCL incl...

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Published inJournal of clinical oncology Vol. 24; no. 6; pp. 953 - 960
Main Authors Besson, Caroline, Canioni, Danielle, Lepage, Eric, Pol, Stanislas, Morel, Pierre, Lederlin, Pierre, Van Hoof, Achiel, Tilly, Hervé, Gaulard, Philippe, Coiffier, Bertrand, Gisselbrecht, Christian, Brousse, Nicole, Reyes, Félix, Hermine, Olivier
Format Journal Article
LanguageEnglish
Published Baltimore, MD American Society of Clinical Oncology 20.02.2006
Lippincott Williams & Wilkins
Subjects
Online AccessGet full text
ISSN0732-183X
1527-7755
1527-7755
DOI10.1200/JCO.2005.01.5016

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Abstract Epidemiologic studies show an association between hepatitis C virus (HCV) and B-cell non-Hodgkin's lymphoma (NHL). Treatment and outcome of patients with diffuse large-cell lymphoma (DLCL) and HCV infection are still a matter of debate. We studied the HCV-positive patients with B-cell DLCL included in the Groupe d'Etude des Lymphomes de l'Adulte (GELA) programs LNH 93 and LNH 98. They were compared with the other patients with DLCL included in these programs. HCV infection prevalence was 0.5% (26 of 5,586 patients). Histologic types of HCV-positive DLCL were more frequently transformed from low-grade lymphoma than DLCL in HCV-negative patients (32% v 6%, P = .02). This is also supported by more frequent spleen involvement in HCV-positive patients (46% v 17%, P < .001). HCV-positive patients had more frequently elevated lactate dehydrogenase levels than other patients (77% v 55%, P = .02). Outcome of HCV-positive patients was poorer for overall survival (P = .02) but not for event-free survival (P = .13). After matching on age and prognosis factors, at 2 years of follow-up, the overall survival was 56% (95% CI, 33% to 76%) among HCV-positive patients, versus 80% (70% to 89%), and the event-free survival was 53% (33% to 72%) versus 74% (64% to 84%). The short-term hepatic toxicity of chemotherapy was strongly increased among HCV-positive patients. After exclusion of the two subjects with chronic hepatitis B virus infection, the overall proportion of subjects undergoing hepatic toxicity was 65% (15 of 23 patients). HCV-positive patients with DLCL differ from other patients both at presentation and during chemotherapy. Specific protocols evaluating antiviral therapy should be designed for these patients.
AbstractList Epidemiologic studies show an association between hepatitis C virus (HCV) and B-cell non-Hodgkin's lymphoma (NHL). Treatment and outcome of patients with diffuse large-cell lymphoma (DLCL) and HCV infection are still a matter of debate. We studied the HCV-positive patients with B-cell DLCL included in the Groupe d'Etude des Lymphomes de l'Adulte (GELA) programs LNH 93 and LNH 98. They were compared with the other patients with DLCL included in these programs. HCV infection prevalence was 0.5% (26 of 5,586 patients). Histologic types of HCV-positive DLCL were more frequently transformed from low-grade lymphoma than DLCL in HCV-negative patients (32% v 6%, P = .02). This is also supported by more frequent spleen involvement in HCV-positive patients (46% v 17%, P < .001). HCV-positive patients had more frequently elevated lactate dehydrogenase levels than other patients (77% v 55%, P = .02). Outcome of HCV-positive patients was poorer for overall survival (P = .02) but not for event-free survival (P = .13). After matching on age and prognosis factors, at 2 years of follow-up, the overall survival was 56% (95% CI, 33% to 76%) among HCV-positive patients, versus 80% (70% to 89%), and the event-free survival was 53% (33% to 72%) versus 74% (64% to 84%). The short-term hepatic toxicity of chemotherapy was strongly increased among HCV-positive patients. After exclusion of the two subjects with chronic hepatitis B virus infection, the overall proportion of subjects undergoing hepatic toxicity was 65% (15 of 23 patients). HCV-positive patients with DLCL differ from other patients both at presentation and during chemotherapy. Specific protocols evaluating antiviral therapy should be designed for these patients.
Epidemiologic studies show an association between hepatitis C virus (HCV) and B-cell non-Hodgkin's lymphoma (NHL). Treatment and outcome of patients with diffuse large-cell lymphoma (DLCL) and HCV infection are still a matter of debate.PURPOSEEpidemiologic studies show an association between hepatitis C virus (HCV) and B-cell non-Hodgkin's lymphoma (NHL). Treatment and outcome of patients with diffuse large-cell lymphoma (DLCL) and HCV infection are still a matter of debate.We studied the HCV-positive patients with B-cell DLCL included in the Groupe d'Etude des Lymphomes de l'Adulte (GELA) programs LNH 93 and LNH 98. They were compared with the other patients with DLCL included in these programs. HCV infection prevalence was 0.5% (26 of 5,586 patients).PATIENTS AND METHODSWe studied the HCV-positive patients with B-cell DLCL included in the Groupe d'Etude des Lymphomes de l'Adulte (GELA) programs LNH 93 and LNH 98. They were compared with the other patients with DLCL included in these programs. HCV infection prevalence was 0.5% (26 of 5,586 patients).Histologic types of HCV-positive DLCL were more frequently transformed from low-grade lymphoma than DLCL in HCV-negative patients (32% v 6%, P = .02). This is also supported by more frequent spleen involvement in HCV-positive patients (46% v 17%, P < .001). HCV-positive patients had more frequently elevated lactate dehydrogenase levels than other patients (77% v 55%, P = .02). Outcome of HCV-positive patients was poorer for overall survival (P = .02) but not for event-free survival (P = .13). After matching on age and prognosis factors, at 2 years of follow-up, the overall survival was 56% (95% CI, 33% to 76%) among HCV-positive patients, versus 80% (70% to 89%), and the event-free survival was 53% (33% to 72%) versus 74% (64% to 84%). The short-term hepatic toxicity of chemotherapy was strongly increased among HCV-positive patients. After exclusion of the two subjects with chronic hepatitis B virus infection, the overall proportion of subjects undergoing hepatic toxicity was 65% (15 of 23 patients).RESULTSHistologic types of HCV-positive DLCL were more frequently transformed from low-grade lymphoma than DLCL in HCV-negative patients (32% v 6%, P = .02). This is also supported by more frequent spleen involvement in HCV-positive patients (46% v 17%, P < .001). HCV-positive patients had more frequently elevated lactate dehydrogenase levels than other patients (77% v 55%, P = .02). Outcome of HCV-positive patients was poorer for overall survival (P = .02) but not for event-free survival (P = .13). After matching on age and prognosis factors, at 2 years of follow-up, the overall survival was 56% (95% CI, 33% to 76%) among HCV-positive patients, versus 80% (70% to 89%), and the event-free survival was 53% (33% to 72%) versus 74% (64% to 84%). The short-term hepatic toxicity of chemotherapy was strongly increased among HCV-positive patients. After exclusion of the two subjects with chronic hepatitis B virus infection, the overall proportion of subjects undergoing hepatic toxicity was 65% (15 of 23 patients).HCV-positive patients with DLCL differ from other patients both at presentation and during chemotherapy. Specific protocols evaluating antiviral therapy should be designed for these patients.CONCLUSIONHCV-positive patients with DLCL differ from other patients both at presentation and during chemotherapy. Specific protocols evaluating antiviral therapy should be designed for these patients.
Author Achiel Van Hoof
Hervé Tilly
Stanislas Pol
Caroline Besson
Nicole Brousse
Pierre Lederlin
Danielle Canioni
Olivier Hermine
Philippe Gaulard
Eric Lepage
Christian Gisselbrecht
Félix Reyes
Pierre Morel
Bertrand Coiffier
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  organization: From the Service d'Hématologie, Service d'Anatomo-Pathologie; Service d'Hépatologie, Hôpital Necker-Enfants Malades, APHP; Université René Descartes CNRS; Institut d'Hématologie, Hôpital Saint-Louis, INSERM ERM 0220, Paris; Service d'Hématologie, Hôpital Bicêtre, Le Kremlin Bicêtre; Département d'Information Hospitalier, Département de Pathologie; Hôpital Henri-Mondor, Créteil; Service d'hématologie, Hôpital de Lens; Service d'Hématologie, CHU Nancy Brabois; Département d'Immunologie, AZ Saint Jan
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  givenname: Danielle
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  givenname: Stanislas
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  organization: From the Service d'Hématologie, Service d'Anatomo-Pathologie; Service d'Hépatologie, Hôpital Necker-Enfants Malades, APHP; Université René Descartes CNRS; Institut d'Hématologie, Hôpital Saint-Louis, INSERM ERM 0220, Paris; Service d'Hématologie, Hôpital Bicêtre, Le Kremlin Bicêtre; Département d'Information Hospitalier, Département de Pathologie; Hôpital Henri-Mondor, Créteil; Service d'hématologie, Hôpital de Lens; Service d'Hématologie, CHU Nancy Brabois; Département d'Immunologie, AZ Saint Jan
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  organization: From the Service d'Hématologie, Service d'Anatomo-Pathologie; Service d'Hépatologie, Hôpital Necker-Enfants Malades, APHP; Université René Descartes CNRS; Institut d'Hématologie, Hôpital Saint-Louis, INSERM ERM 0220, Paris; Service d'Hématologie, Hôpital Bicêtre, Le Kremlin Bicêtre; Département d'Information Hospitalier, Département de Pathologie; Hôpital Henri-Mondor, Créteil; Service d'hématologie, Hôpital de Lens; Service d'Hématologie, CHU Nancy Brabois; Département d'Immunologie, AZ Saint Jan
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  organization: From the Service d'Hématologie, Service d'Anatomo-Pathologie; Service d'Hépatologie, Hôpital Necker-Enfants Malades, APHP; Université René Descartes CNRS; Institut d'Hématologie, Hôpital Saint-Louis, INSERM ERM 0220, Paris; Service d'Hématologie, Hôpital Bicêtre, Le Kremlin Bicêtre; Département d'Information Hospitalier, Département de Pathologie; Hôpital Henri-Mondor, Créteil; Service d'hématologie, Hôpital de Lens; Service d'Hématologie, CHU Nancy Brabois; Département d'Immunologie, AZ Saint Jan
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Snippet Epidemiologic studies show an association between hepatitis C virus (HCV) and B-cell non-Hodgkin's lymphoma (NHL). Treatment and outcome of patients with...
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Antineoplastic Combined Chemotherapy Protocols - adverse effects
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Antiviral Agents - therapeutic use
Biological and medical sciences
Disease-Free Survival
Female
Hepatitis C - complications
Hepatitis C - drug therapy
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Lymphoma, Large B-Cell, Diffuse - virology
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Title 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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