Immunotherapy Responses in Viral Hepatitis-Induced HCC: A Systematic Review and Meta-Analysis
Junaid Anwar1, Hafiz Muhammad Arslan2, Zouina Sarfraz3
1Department of Medicine, Baptist Hospitals of Southeast Texas, Beaumont, TX 77701, USA.
Immunotherapy offers improved outcomes for hepatocellular carcinoma (HCC), especially in viral hepatitis-associated cases. Viral HCC patients showed significantly better progression-free and overall survival compared to non-viral HCC patients.
Area of Science:
- Oncology
- Hepatology
- Immunology
Background:
- Hepatocellular carcinoma (HCC) is a leading cause of cancer death globally, frequently associated with hepatitis B (HBV) and C (HCV) viral infections.
- Existing treatments for HCC often yield suboptimal prognoses, underscoring the need for novel therapeutic strategies.
- Immunotherapy has emerged as a promising modality for various cancers, including HCC.
Approach:
- A comprehensive meta-analysis was conducted adhering to PRISMA Statement 2020 guidelines.
- Data from 9 randomized controlled trials, involving 5316 patients, were analyzed up to April 2024.
- Outcomes including objective response rate (ORR), progression-free survival (PFS), and overall survival (OS) were evaluated using fixed-effects models.
Key Points:
- While objective response rates (ORR) did not significantly differ between viral and non-viral HCC groups, viral HCC patients demonstrated significantly improved progression-free survival (PFS) (p=0.005) and overall survival (OS) (p<0.0001).
- Median PFS was 7.3 months for viral HCC versus 5.8 months for non-viral HCC.
- Median OS was 16.8 months for viral HCC versus 15.2 months for non-viral HCC.
Conclusions:
- Immunotherapy demonstrates significant efficacy in treating hepatocellular carcinoma (HCC), particularly in patients with viral hepatitis B (HBV) or C (HCV) infections.
- Hepatocellular carcinoma associated with viral hepatitis shows superior survival outcomes with immunotherapy compared to non-viral etiologies.
- Personalized treatment strategies considering the viral etiology of HCC are crucial for optimizing immunotherapy outcomes.
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