Poor Prognosis of Diffuse Large B-Cell Lymphoma with Hepatitis C Infection

被引:6
作者
Tsai, Yu-Fen [1 ,2 ]
Liu, Yi-Chang [3 ,4 ]
Yang, Ching-, I [3 ,5 ]
Chuang, Tzer-Ming [3 ]
Ke, Ya-Lun [3 ]
Yeh, Tsung-Jang [3 ]
Gau, Yuh-Ching [3 ]
Du, Jeng-Shiun [3 ]
Wang, Hui-Ching [3 ,4 ]
Cho, Shih-Feng [3 ,4 ]
Hsu, Chin-Mu [3 ]
Wu, Pey-Fang [6 ]
Huang, Ching-, I [4 ,6 ]
Huang, Chung-Feng [4 ,6 ]
Yu, Ming-Lung [4 ,6 ]
Dai, Chia-Yen [4 ,6 ]
Hsiao, Hui-Hua [3 ,4 ,7 ,8 ]
机构
[1] E Da Canc Hosp, Dept Hematol & Oncol, Kaohsiung 824, Taiwan
[2] I Shou Univ, Coll Med, Sch Chinese Med Post Baccalaureate, Kaohsiung 824, Taiwan
[3] Kaohsiung Med Univ Hosp, Dept Internal Med, Div Hematol & Oncol, Kaohsiung 807, Taiwan
[4] Kaohsiung Med Univ, Fac Med, Kaohsiung 807, Taiwan
[5] Kaohsiung Med Univ, Kaohsiung Med Univ Hosp, Specialist Nurse & Surg Nurse Practitioner Off, Kaohsiung 807, Taiwan
[6] Kaohsiung Med Univ Hosp, Dept Internal Med, Div Hepatobiliary Ward, Kaohsiung 807, Taiwan
[7] Kaohsiung Med Univ, Ctr Liquid Biopsy, Kaohsiung 807, Taiwan
[8] Kaohsiung Med Univ, Kaohsiung Med Univ Hosp, Canc Ctr, Kaohsiung 807, Taiwan
关键词
hepatitis C virus; diffuse large B-cell lymphoma; survival; fibrosis; performance status; liver toxicity; NON-HODGKIN-LYMPHOMA; VIRUS-POSITIVE PATIENTS; TAIWAN; FIBROSIS; RISK; PREVALENCE; RITUXIMAB; TOXICITY; THERAPY; MODEL;
D O I
10.3390/jpm11090844
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background: Hepatitis C virus (HCV) in diffuse large B-cell lymphoma (DLBCL) is associated with a higher prevalence and distinctive clinical characteristics and outcomes. Methods: A retrospective analysis of adult DLBCL patients from 2011 to 2015 was studied. Results: A total of 206 adult DLBCL were enrolled with 22 (10.7%) HCV-positive patients. Compared to HCV-negative patients, the HCV-positive group had a poor performance status (p = 0.011), lower platelet count (p = 0.029), and higher spleen and liver involvement incidences (liver involvement, p = 0.027, spleen involvement, p = 0.026), and they received fewer cycles of chemotherapy significantly due to morbidity and mortality (p = 0.048). Overall survival was shorter in HCV-positive DLBCL (25.3 months in HCV-positive vs. not reached (NR), p = 0.049). With multivariate analysis, poor performance status (p < 0.001), advanced stage (p < 0.001), less chemotherapy cycles (p < 0.001), and the presence of liver toxicity (p = 0.001) contributed to poor OS in DLBCL. Among HCV-positive DLBCL, the severity of liver fibrosis was the main risk factor related to death. Conclusion: Inferior survival of HCV-positive DLBCL was observed and associated with poor performance status, higher numbers of complications, and intolerance of treatment, leading to fewer therapy. Therefore, anti-HCV therapy, such as direct-acting antiviral agents, might benefit these patients in the future.
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页数:13
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