Early antiviral therapy reduces the risk of lymphoma in patients with chronic hepatitis C infection

被引:10
作者
Su, Tung-Hung [1 ,2 ]
Liu, Chun-Jen [1 ,2 ]
Tseng, Tai-Chung [1 ,2 ]
Chou, Shih-Wan [1 ]
Liu, Chen-Hua [1 ,2 ]
Yang, Hung-Chih [1 ]
Wu, Shang-Ju [3 ]
Chen, Pei-Jer [1 ,2 ,4 ,5 ]
Chen, Ding-Shinn [1 ,2 ,4 ,6 ]
Chen, Chi-Ling [4 ]
Kao, Jia-Horng [1 ,2 ,4 ,5 ]
机构
[1] Natl Taiwan Univ Hosp, Div Gastroenterol & Hepatol, Dept Internal Med, Taipei, Taiwan
[2] Natl Taiwan Univ Hosp, Hepatitis Res Ctr, Taipei, Taiwan
[3] Natl Taiwan Univ Hosp, Div Hematol, Dept Internal Med, Taipei, Taiwan
[4] Natl Taiwan Univ, Grad Inst Clin Med, Coll Med, Taipei, Taiwan
[5] Natl Taiwan Univ Hosp, Dept Med Res, Taipei, Taiwan
[6] Acad Sinica, Genom Res Ctr, Taipei, Taiwan
关键词
NON-HODGKINS-LYMPHOMA; MARGINAL ZONE LYMPHOMA; B-CELL; PEGYLATED-INTERFERON; LYMPHOPROLIFERATIVE DISORDERS; VIRUS-INFECTION; EPIDEMIOLOGY; REGRESSION; RIBAVIRIN; POPULATION;
D O I
10.1111/apt.15101
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background Chronic hepatitis C infection is linked to lymphoma development. Aim To investigate whether antiviral therapy prevents the risk of HCV-related lymphoma. Methods Patients diagnosed with chronic hepatitis C were retrieved from the Taiwan National Health Insurance Research Database during 2004-2012. We included patients who received pegylated interferon and ribavirin (PegIFN/RBV) antiviral therapy for >= 24 weeks (PegIFN/RBV cohort) or hepatoprotectants for >= 90 days without antiviral therapy (HCV-untreated cohort). Both cohorts were matched by age, sex, and comorbidities through propensity scores and followed for newly diagnosed lymphoma or non-Hodgkin's lymphoma (NHL). Results In total, 24 133 patients were included in both the PegIFN/RBV and HCV-untreated cohort. The lymphoma incidence was significantly higher in the untreated than in the treated cohort (66.48 vs 43.34 per 100 000 person-years, P = 0.029). After adjusting for confounders, the patients who received PegIFN/RBV therapy were at a lower risk of developing lymphoma compared with the untreated patients (hazard ratio [HR]: 0.64, 95% confidence interval [CI]: 0.43-0.96, P = 0.030). Moreover, this beneficial effect was mainly observed in patients with chronic hepatitis C <60 years old with a relative risk reduction of 51% for all lymphoma (HR: 0.49, 95% CI: 0.29-0.82, P = 0.007) and 48% for non-Hodgkin's lymphoma (HR: 0.52, 95% CI: 0.30-0.91, P = 0.022). The risk of all lymphoma or non-Hodgkin's lymphoma development after antiviral therapy was lowered to that of subjects without HCV. Conclusions PegIFN/RBV-based antiviral therapy significantly reduced the risk of lymphoma, especially non-Hodgkin's lymphoma; the reduction was mostly among patients <60 years old. Early antiviral therapy for chronic hepatitis C is suggested.
引用
收藏
页码:331 / 339
页数:9
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