Clinical trial · Observational
Viral Load Changes in Lymphoma Patients With HCV Infection After Chemotherapy
Serial Viral Load Changes and Hepatotoxicity in Lymphoma Patients With Hepatitis C Antibody After Chemotherapy Treatment: A Prospective Multicenter Observational Study and Long-term Retrospective Analysis
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
In last few years, most researches about hepatic complication after chemotherapy focused on hepatitis B virus (HBV). With adequate prophylaxis and monitor, HBV-related hepatitis flares can be prevented. In contrast, cancer patients with hepatitis C virus (HCV) infection are traditionally considered as relative safe to receive chemotherapy. However, two large retrospective studies recently showed that severe hepatitis could develop in 14-27% lymphoma patients with chronic HCV infection, including 3-4% hepatic failure. The risk factors to predict severe hepatitis are pre-treatment elevated ALT level and liver cirrhosis. Due to the lack of prospective studies, the dynamic changes of serum HCV RNA levels and the association of hepatitis are still unclear. Some epidemiologic studies demonstrated an association between HCV infection and B-cell lymphoma. Diffuse large B-cell lymphoma (DLBCL) is the most common lymphoma and several reports showed higher prevalence of HCV infection among DLBCL patients than the controls. HCV infected DLBCL patients are reported to have distinct clinical characteristics, such as older, more with elevated LDH levels, and more with extra-nodal involvement. Regarding the impact of HCV infection on prognosis, the results are conflicting. Taiwan is an endemic area of HCV but there are limited reports addressing the clinical characteristics and prognosis in this unique population. Therefore, the investigators initiate a prospective, multi-center observational study to clarify the dynamic association between serum HCV RNA levels and hepatitis in HCV-infected lymphoma patients treated with chemotherapy.
Conditions
Conditions (3)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Drug Therapy | — | UNRESOLVED | — |
| Hepatitis C Antibodies | — | UNRESOLVED | — |
| Lymphoma | Lymphoma | ONTOLOGY_EXACT | 0.90 |
Interventions
Interventions (0)
Data not yet available
Design
Arms and outcomes
Arms (1)
- label
- HCV lymphoma patients with chemotherapy
- description
- Lymphoma patients who are positive for anti-HCV and are planning to receive chemotherapy for lymphoma
Primary outcomes (4)
- measure
- Number of Participants with Increasing HCV RNA Level and Developing Hepatitis after Chemotherapy
- timeFrame
- one year
- measure
- Number of Participants with Detectable Viremia and Developing Hepatitis after Chemotherapy
- timeFrame
- one year
- measure
- Interval (months) between Peak HCV RNA Level and Hepatitis
- timeFrame
- one year
- measure
- Increase (log) of HCV Viral Load between Baseline and after Chemotherapy
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 20 Years
Show eligibility criteria text
Inclusion Criteria: 1. Newly diagnosed histologically proven malignant lymphoma 2. Eligible subjects must be positive for anti-HCV Ab 3. Age ≥ 20 years 4. Planned to receive chemotherapy 5. No recent chemotherapy and radiotherapy in the past one year. Pre-enrollment steroids for symptomatic relief are allowed but less than equivalent dose to prednisolone total 140 mg 6. Left expectancy ≥ 3 months 7. Signed informed consent 8. ECOG 0-2 Exclusion Criteria: 1. Patients not willing to receive chemotherapy 2. Chronic hepatitis B infection (positive for HBsAg), but those with resolved HBV infection (positive for anti-HBc and negative for HBsAg) are allowed 3. Other major systemic diseases, such as active infection, significant cardiac disease, neurologic deficit or psychiatric disorders, that the investigators consider to be at significant risk 4. Known human immunodeficiency virus (HIV) infection 5. Pregnant or breast-feeding woman
References
Publications (0)
Data not yet available