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DOI 10.1111/jvh.70032

Медицинская библиотека · Journal of viral hepatitis · 2025

Leading Role of Sofosbuvir/Daclatasvir in Achieving Hepatitis C Elimination in Egypt.

Elbaz Tamer, Al-Naamani Khalid, Abosheaishaa Hazem, Alswat Khalid, El-Kassas Mohamed

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Аннотация

Chronic hepatitis C virus (HCV) management has historically been challenging, particularly in Egypt, the country with the highest global disease prevalence. The introduction of direct-acting antivirals (DAAs) has revolutionised treatment, providing high rates of sustained virologic response (SVR) with fewer adverse events compared to previous therapies. In Egypt, the locally produced generics of sofosbuvir/daclatasvir (SOF/DAC) have been integral to the national HCV elimination programme, treating millions effectively and affordably, demonstrating similar efficacy and safety to brand-name drugs. Although not currently present in most international guidelines, this cost-effective regimen offers a viable option for large-scale elimination programmes similar to Egypt's successful experience. This review synthesises real-world Egyptian data and highlights the efficacy and safety of the SOF/DAC combination in various population groups. High sustained virological response (SVR) rates were observed across diverse patient populations, including those with advanced liver disease. However, limitations regarding long-term follow-up, especially HCC surveillance, were identified, underscoring the need for further research. Additionally, the review underscores the success of local Egyptian pharmaceutical policies in reducing treatment costs and securing access for all infected individuals. The Egyptian experience offers valuable insights into the potential for replicating its success, particularly in other high-burden regions.

Для цитирования: Elbaz Tamer, Al-Naamani Khalid, Abosheaishaa Hazem, Alswat Khalid, El-Kassas Mohamed. Leading Role of Sofosbuvir/Daclatasvir in Achieving Hepatitis C Elimination in Egypt.. Journal of viral hepatitis. 2025. DOI: 10.1111/jvh.70032.

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