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 in | Journal of clinical oncology Vol. 24; no. 6; pp. 953 - 960 |
|---|---|
| Main Authors | , , , , , , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Baltimore, MD
American Society of Clinical Oncology
20.02.2006
Lippincott Williams & Wilkins |
| Subjects | |
| Online Access | Get full text |
| ISSN | 0732-183X 1527-7755 1527-7755 |
| DOI | 10.1200/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. |
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| 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 |
| Author_xml | – sequence: 1 givenname: Caroline surname: Besson fullname: Besson, Caroline 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 – sequence: 2 givenname: Danielle surname: Canioni fullname: Canioni, Danielle 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 – sequence: 3 givenname: Eric surname: Lepage fullname: Lepage, Eric 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 – sequence: 4 givenname: Stanislas surname: Pol fullname: Pol, Stanislas 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; 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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 – sequence: 7 givenname: Achiel surname: Van Hoof fullname: Van Hoof, Achiel 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 – sequence: 8 givenname: Hervé surname: Tilly fullname: Tilly, Hervé 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 – sequence: 9 givenname: Philippe surname: Gaulard fullname: Gaulard, Philippe 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 – sequence: 10 givenname: Bertrand surname: Coiffier fullname: Coiffier, Bertrand organization: From the Service d'Hématologie, Service d'Anatomo-Pathologie; 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| BackLink | http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17549000$$DView record in Pascal Francis https://www.ncbi.nlm.nih.gov/pubmed/16418500$$D View this record in MEDLINE/PubMed |
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| ContentType | Journal Article |
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| SubjectTerms | Adult Aged Antineoplastic Combined Chemotherapy Protocols - adverse effects Antineoplastic Combined Chemotherapy Protocols - therapeutic use Antiviral Agents - therapeutic use Biological and medical sciences Disease-Free Survival Female Hepatitis C - complications Hepatitis C - drug therapy Hepatitis C Antigens - blood Humans Immunohistochemistry Incidence Liver - drug effects Lymphoma, B-Cell - drug therapy Lymphoma, B-Cell - virology Lymphoma, Large B-Cell, Diffuse - drug therapy Lymphoma, Large B-Cell, Diffuse - virology Male Medical sciences Middle Aged Seroepidemiologic Studies Severity of Illness Index Spleen - pathology Spleen - virology Survival Analysis Treatment Outcome Tumors |
| 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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