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First-Line Durvalumab-Tremelimumab in Advanced Hepatocellular Carcinoma: Real-World Data from Turkey
Mustafa Murat Mıdık1, Gökhan Şahin1, Bekir Mert Durukan2
1Department of Medical Oncology, Ege University Medical Faculty, 35100 Izmir, Turkey.
First-line STRIDE therapy (durvalumab plus tremelimumab) showed feasibility and good tolerability in unresectable hepatocellular carcinoma (HCC) patients in a real-world Turkish setting. Further prospective studies are needed for confirmation.
Area of Science:
- Oncology
- Hepatology
- Immunotherapy
Background:
- Hepatocellular carcinoma (HCC) is a major global cause of cancer mortality.
- The STRIDE regimen (durvalumab plus tremelimumab) shows promise, but real-world data, especially in Turkey, is scarce.
- This study addresses the need for real-world effectiveness and safety data of first-line STRIDE therapy for unresectable HCC.
Purpose of the Study:
- To evaluate the real-world effectiveness and safety of first-line durvalumab plus tremelimumab (STRIDE regimen) in unresectable HCC patients.
- To assess progression-free survival (PFS) and overall survival (OS) in a routine clinical practice setting.
- To identify potential prognostic factors influencing treatment outcomes.
Main Methods:
- Retrospective multicenter study involving 32 patients with unresectable HCC treated with first-line durvalumab plus tremelimumab.
- Data collected through the Turkish national Early Access Program across 18 oncology centers.
- Kaplan-Meier method for PFS and OS estimation; exploratory Cox regression for prognostic factors.
Main Results:
- Median PFS was 7.25 months; median OS was 11.43 months.
- Non-viral liver disease was the most common etiology (53.1%), followed by HBV (40.6%) and HCV (6.3%).
- Grade ≥ 3 treatment-related adverse events were infrequent (<10% of patients).
Conclusions:
- First-line durvalumab plus tremelimumab appears feasible and well-tolerated in a real-world cohort of unresectable HCC patients.
- Findings suggest potential efficacy, but should be interpreted cautiously due to study limitations.
- Larger, prospective, comparative studies are required to validate these real-world observations.
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