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Published on: September 25, 2019
Viral elimination reduces incidence of malignant lymphoma in patients with hepatitis C
Yusuke Kawamura1, Kenji Ikeda, Yasuji Arase
1Department of Hepatology, Toranomon Hospital, Tokyo, Japan. k-yusuke@toranomon.gr.jp
Insights
Hepatitis C virus (HCV) patients who achieve sustained virologic response through interferon therapy show a significantly lower risk of developing malignant lymphoma. Viral elimination protects against lymphomagenesis in HCV-infected individuals.
Area of Science:
- Hepatology
- Oncology
- Virology
Background:
- Hepatitis C virus (HCV) infection is associated with a higher incidence of malignant lymphoma.
- Understanding the relationship between HCV, viral elimination, and lymphoma development is crucial for patient management.
Purpose of the Study:
- To determine the incidence of malignant lymphoma in HCV-infected patients.
- To investigate the association between malignant lymphoma and viral elimination after interferon therapy.
Main Methods:
- Retrospective study of 501 HCV patients without interferon therapy and 2708 HCV patients who received interferon therapy.
- Analysis of cumulative incidence rates of malignant lymphoma development over 15 years.
- Comparison of lymphoma development rates between patients with sustained virologic response and persistent infection.
Main Results:
- The annual incidence of malignant lymphoma in HCV patients was found to be 0.23%.
- Patients achieving sustained virologic response (SVR) after interferon therapy had a 0% cumulative incidence of lymphoma at 15 years.
- Patients with persistent HCV infection had significantly higher rates of malignant lymphoma development compared to those with SVR (P=.0159).
- The hazard ratio for lymphomagenesis was significantly lower in patients with SVR (0.13; P=.049).
Conclusions:
- Sustained virologic response induced by interferon therapy offers protection against the development of malignant lymphoma in patients with chronic HCV.
- Interferon therapy and achieving viral elimination are key factors in reducing lymphoma risk in HCV-positive individuals.
Purpose:
A high prevalence of malignant lymphoma among patients with hepatitis C virus (HCV) infection has been reported. The aim of this retrospective study was to determine the incidence of malignant lymphoma and the relationship between malignant lymphoma and viral elimination in patients with HCV.
Method:
We studied 501 consecutive HCV-infected patients who had never received interferon therapy and 2708 consecutive HCV-infected patients who received interferon therapy.
Results:
In the non-interferon group, the cumulative rates of malignant lymphoma development were 0.6% at the 5th year, 2.3% at the 10th year, and 2.6% at the 15th year. The cumulative rates of malignant lymphoma development in interferon-treated patients with sustained virologic response were 0% at the 5th year, 0% at the 10th year, and 0% at the 15th year. The cumulative rates of malignant lymphoma development with persistent infection were 0.4% at the 5th year, 1.5% at the 10th year, and 2.6% at the 15th year. The malignant lymphoma development rate was higher in patients with persistent infection than in patients with sustained virologic response (P=.0159). The hazard ratio of lymphomagenesis in 1048 patients with sustained virologic response was significantly lower than in patients with persistent infection (hazard ratio: 0.13; P=.049).
Conclusion:
Our retrospective study is the first to determine the annual incidence of malignant lymphoma among patients with HCV at 0.23%. Our results indicate that sustained virologic response induced by interferon therapy protects against the development of malignant lymphoma in patients with chronic HCV.
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