Chronic hepatitis virus infection in patients with multiple myeloma: clinical characteristics and outcomes
Autor(a) principal: | |
---|---|
Data de Publicação: | 2011 |
Outros Autores: | , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Clinics |
Texto Completo: | https://www.revistas.usp.br/clinics/article/view/19329 |
Resumo: | OBJECTIVES: Cytotoxic agents and steroids are used to treat lymphoid malignancies, but these compounds may exacerbate chronic viral hepatitis. For patients with multiple myeloma, the impact of preexisting hepatitis virus infection is unclear. The aim of this study is to explore the characteristics and outcomes of myeloma patients with chronic hepatitis virus infection. METHODS: From 2003 to 2008, 155 myeloma patients were examined to determine their chronic hepatitis virus infection statuses using serologic tests for the hepatitis B (HBV) and C viruses (HCV). Clinical parameters and outcome variables were retrieved via a medical chart review. RESULTS: The estimated prevalences of chronic HBV and HCV infections were 11.0% (n = 17) and 9.0% (n = 14), respectively. The characteristics of patients who were hepatitis virus carriers and those who were not were similar. However, carrier patients had a higher prevalence of conventional cytogenetic abnormalities (64.3% vs. 25.0%). The cumulative incidences of grade 3-4 elevation of the level of alanine transaminase, 30.0% vs. 12.0%, and hyperbilirubinemia, 20.0% vs. 1.6%, were higher in carriers as well. In a Kaplan-Meier analysis, carrier patients had worse overall survival (median: 16.0 vs. 42.4 months). The prognostic value of carrier status was not statistically significant in the multivariate analysis, but an age of more than 65 years old, the presence of cytogenetic abnormalities, a beta-2-microglobulin level of more than 3.5 mg/L, and a serum creatinine level of more than 2 mg/ dL were independent factors associated with poor prognosis. CONCLUSION: Myeloma patients with chronic hepatitis virus infections might be a distinct subgroup, and close monitoring of hepatic adverse events should be mandatory. |
id |
USP-19_fb24f9d58a01ce17533c5a59f3e5b8b2 |
---|---|
oai_identifier_str |
oai:revistas.usp.br:article/19329 |
network_acronym_str |
USP-19 |
network_name_str |
Clinics |
repository_id_str |
|
spelling |
Chronic hepatitis virus infection in patients with multiple myeloma: clinical characteristics and outcomes Hepatitis B virusHepatitis C virusMultiple myelomaCytogenetic abnormalitiesAdverse events OBJECTIVES: Cytotoxic agents and steroids are used to treat lymphoid malignancies, but these compounds may exacerbate chronic viral hepatitis. For patients with multiple myeloma, the impact of preexisting hepatitis virus infection is unclear. The aim of this study is to explore the characteristics and outcomes of myeloma patients with chronic hepatitis virus infection. METHODS: From 2003 to 2008, 155 myeloma patients were examined to determine their chronic hepatitis virus infection statuses using serologic tests for the hepatitis B (HBV) and C viruses (HCV). Clinical parameters and outcome variables were retrieved via a medical chart review. RESULTS: The estimated prevalences of chronic HBV and HCV infections were 11.0% (n = 17) and 9.0% (n = 14), respectively. The characteristics of patients who were hepatitis virus carriers and those who were not were similar. However, carrier patients had a higher prevalence of conventional cytogenetic abnormalities (64.3% vs. 25.0%). The cumulative incidences of grade 3-4 elevation of the level of alanine transaminase, 30.0% vs. 12.0%, and hyperbilirubinemia, 20.0% vs. 1.6%, were higher in carriers as well. In a Kaplan-Meier analysis, carrier patients had worse overall survival (median: 16.0 vs. 42.4 months). The prognostic value of carrier status was not statistically significant in the multivariate analysis, but an age of more than 65 years old, the presence of cytogenetic abnormalities, a beta-2-microglobulin level of more than 3.5 mg/L, and a serum creatinine level of more than 2 mg/ dL were independent factors associated with poor prognosis. CONCLUSION: Myeloma patients with chronic hepatitis virus infections might be a distinct subgroup, and close monitoring of hepatic adverse events should be mandatory. Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2011-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/clinics/article/view/1932910.1590/S1807-59322011001200010Clinics; Vol. 66 No. 12 (2011); 2055-2061 Clinics; v. 66 n. 12 (2011); 2055-2061 Clinics; Vol. 66 Núm. 12 (2011); 2055-2061 1980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/19329/21392Teng, Chung-JenLiu, Han-TsungLiu, Chun-YuHsih, Chi-HsiuPai, Jih-TungGau, Jyh-PyngLiu, Jin-HwangChiou, Tzeon-JyeHsu, Hui-ChiChen, Po-MinTzeng, Cheng-HwaiYu, Yuan-Bininfo:eu-repo/semantics/openAccess2012-05-23T16:34:21Zoai:revistas.usp.br:article/19329Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2012-05-23T16:34:21Clinics - Universidade de São Paulo (USP)false |
dc.title.none.fl_str_mv |
Chronic hepatitis virus infection in patients with multiple myeloma: clinical characteristics and outcomes |
title |
Chronic hepatitis virus infection in patients with multiple myeloma: clinical characteristics and outcomes |
spellingShingle |
Chronic hepatitis virus infection in patients with multiple myeloma: clinical characteristics and outcomes Teng, Chung-Jen Hepatitis B virus Hepatitis C virus Multiple myeloma Cytogenetic abnormalities Adverse events |
title_short |
Chronic hepatitis virus infection in patients with multiple myeloma: clinical characteristics and outcomes |
title_full |
Chronic hepatitis virus infection in patients with multiple myeloma: clinical characteristics and outcomes |
title_fullStr |
Chronic hepatitis virus infection in patients with multiple myeloma: clinical characteristics and outcomes |
title_full_unstemmed |
Chronic hepatitis virus infection in patients with multiple myeloma: clinical characteristics and outcomes |
title_sort |
Chronic hepatitis virus infection in patients with multiple myeloma: clinical characteristics and outcomes |
author |
Teng, Chung-Jen |
author_facet |
Teng, Chung-Jen Liu, Han-Tsung Liu, Chun-Yu Hsih, Chi-Hsiu Pai, Jih-Tung Gau, Jyh-Pyng Liu, Jin-Hwang Chiou, Tzeon-Jye Hsu, Hui-Chi Chen, Po-Min Tzeng, Cheng-Hwai Yu, Yuan-Bin |
author_role |
author |
author2 |
Liu, Han-Tsung Liu, Chun-Yu Hsih, Chi-Hsiu Pai, Jih-Tung Gau, Jyh-Pyng Liu, Jin-Hwang Chiou, Tzeon-Jye Hsu, Hui-Chi Chen, Po-Min Tzeng, Cheng-Hwai Yu, Yuan-Bin |
author2_role |
author author author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Teng, Chung-Jen Liu, Han-Tsung Liu, Chun-Yu Hsih, Chi-Hsiu Pai, Jih-Tung Gau, Jyh-Pyng Liu, Jin-Hwang Chiou, Tzeon-Jye Hsu, Hui-Chi Chen, Po-Min Tzeng, Cheng-Hwai Yu, Yuan-Bin |
dc.subject.por.fl_str_mv |
Hepatitis B virus Hepatitis C virus Multiple myeloma Cytogenetic abnormalities Adverse events |
topic |
Hepatitis B virus Hepatitis C virus Multiple myeloma Cytogenetic abnormalities Adverse events |
description |
OBJECTIVES: Cytotoxic agents and steroids are used to treat lymphoid malignancies, but these compounds may exacerbate chronic viral hepatitis. For patients with multiple myeloma, the impact of preexisting hepatitis virus infection is unclear. The aim of this study is to explore the characteristics and outcomes of myeloma patients with chronic hepatitis virus infection. METHODS: From 2003 to 2008, 155 myeloma patients were examined to determine their chronic hepatitis virus infection statuses using serologic tests for the hepatitis B (HBV) and C viruses (HCV). Clinical parameters and outcome variables were retrieved via a medical chart review. RESULTS: The estimated prevalences of chronic HBV and HCV infections were 11.0% (n = 17) and 9.0% (n = 14), respectively. The characteristics of patients who were hepatitis virus carriers and those who were not were similar. However, carrier patients had a higher prevalence of conventional cytogenetic abnormalities (64.3% vs. 25.0%). The cumulative incidences of grade 3-4 elevation of the level of alanine transaminase, 30.0% vs. 12.0%, and hyperbilirubinemia, 20.0% vs. 1.6%, were higher in carriers as well. In a Kaplan-Meier analysis, carrier patients had worse overall survival (median: 16.0 vs. 42.4 months). The prognostic value of carrier status was not statistically significant in the multivariate analysis, but an age of more than 65 years old, the presence of cytogenetic abnormalities, a beta-2-microglobulin level of more than 3.5 mg/L, and a serum creatinine level of more than 2 mg/ dL were independent factors associated with poor prognosis. CONCLUSION: Myeloma patients with chronic hepatitis virus infections might be a distinct subgroup, and close monitoring of hepatic adverse events should be mandatory. |
publishDate |
2011 |
dc.date.none.fl_str_mv |
2011-01-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://www.revistas.usp.br/clinics/article/view/19329 10.1590/S1807-59322011001200010 |
url |
https://www.revistas.usp.br/clinics/article/view/19329 |
identifier_str_mv |
10.1590/S1807-59322011001200010 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://www.revistas.usp.br/clinics/article/view/19329/21392 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo |
publisher.none.fl_str_mv |
Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo |
dc.source.none.fl_str_mv |
Clinics; Vol. 66 No. 12 (2011); 2055-2061 Clinics; v. 66 n. 12 (2011); 2055-2061 Clinics; Vol. 66 Núm. 12 (2011); 2055-2061 1980-5322 1807-5932 reponame:Clinics instname:Universidade de São Paulo (USP) instacron:USP |
instname_str |
Universidade de São Paulo (USP) |
instacron_str |
USP |
institution |
USP |
reponame_str |
Clinics |
collection |
Clinics |
repository.name.fl_str_mv |
Clinics - Universidade de São Paulo (USP) |
repository.mail.fl_str_mv |
||clinics@hc.fm.usp.br |
_version_ |
1800222756777754624 |