Real-world outcomes and predictive factors in hepatocellular carcinoma patients treated with sorafenib: an 18-month ambispective cohort analysis

Abstract Background Hepatocellular carcinoma (HCC) represents 90% of primary liver cancers and is the fourth leading cause of cancer-related death worldwide. Sorafenib remains the standard first-line systemic therapy for advanced HCC, though real-world outcomes vary from clinical trial results. We aimed to evaluate survival outcomes and identify prognostic factors in HCC patients receiving sorafenib in routine clinical practice over an 18-month follow-up period in a real-world clinical setting. Methods An ambispective cohort study (integrating retrospective and prospective data) was conducted involving 347 patients with confirmed primary HCC treated with Sorafenib between June 2023 and January 2025, of whom 292 had complete 18-month follow-up and were included in the survival analysis . Clinical data, laboratory markers, imaging Response Evaluation Criteria In Solid Tumors (RECIST 1.1), adverse effects, and treatment modifications were analyzed. Kaplan–Meier analysis and Cox regression models were used to determine overall survival (OS), progression-free survival (PFS), and prognostic predictors. Results The observed OS rates at 6, 12, and 18 months were 69.3%, 45.2%, and 31.1%, respectively. Corresponding PFS rates were 58.6%, 36.9%, and 24.8%. In multivariate analysis, Eastern Cooperative Oncology Group (ECOG) performance status ≥ 1, AFP > 400 ng/mL, Albumin-Bilirubin (ALBI) grade 3, and vascular invasion were significantly associated with reduced OS ( p < 0.05). Patients who achieved partial response or stable disease per RECIST were more likely to continue Sorafenib beyond 6 months. Toxicity was generally tolerable, with a low rate of permanent treatment discontinuation. Conclusion Sorafenib continues to demonstrate efficacy in real-world practice as first-line therapy for advanced HCC, with clear clinical and biochemical indicators, including ALBI grade, AFP, ECOG, and early radiological response, serving as key prognostic factors of treatment success. Early response assessment with identification of poor prognostic factors is critical for optimizing outcomes, and proactive toxicity management can improve outcomes in real-world settings.

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Publication Details

Journal
Future Journal of Pharmaceutical Sciences
Published
2025-10-20
DOI
https://doi.org/10.1186/s43094-025-00892-6
Citations
1
Primary Topic
Hepatocellular Carcinoma Treatment and Prognosis
Type
article
Field-Weighted Citation Impact
1.32
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article

Real-world outcomes and predictive factors in hepatocellular carcinoma patients treated with sorafenib: an 18-month ambispective cohort analysis

Imam Waked, Mohamed Abdel-Latif, Sahar B. Hassan, Ahmed I. Khoder et al.
1 citations
Future Journal of Pharmaceutical Sciences
Hepatocellular Carcinoma Treatment and Prognosis
1.32
article

Real-world outcomes and predictive factors in hepatocellular carcinoma patients treated with sorafenib: an 18-month ambispective cohort analysis

Imam Waked, Mohamed Abdel-Latif, Sahar B. Hassan, Ahmed I. Khoder, Shimaa Abdelsattar, Mahmoud Nazih, Mohamed S. El Senbawy
article en
1 citations

Abstract

Abstract Background Hepatocellular carcinoma (HCC) represents 90% of primary liver cancers and is the fourth leading cause of cancer-related death worldwide. Sorafenib remains the standard first-line systemic therapy for advanced HCC, though real-world outcomes vary from clinical trial results. We aimed to evaluate survival outcomes and identify prognostic factors in HCC patients receiving sorafenib in routine clinical practice over an 18-month follow-up period in a real-world clinical setting. Methods An ambispective cohort study (integrating retrospective and prospective data) was conducted involving 347 patients with confirmed primary HCC treated with Sorafenib between June 2023 and January 2025, of whom 292 had complete 18-month follow-up and were included in the survival analysis . Clinical data, laboratory markers, imaging Response Evaluation Criteria In Solid Tumors (RECIST 1.1), adverse effects, and treatment modifications were analyzed. Kaplan–Meier analysis and Cox regression models were used to determine overall survival (OS), progression-free survival (PFS), and prognostic predictors. Results The observed OS rates at 6, 12, and 18 months were 69.3%, 45.2%, and 31.1%, respectively. Corresponding PFS rates were 58.6%, 36.9%, and 24.8%. In multivariate analysis, Eastern Cooperative Oncology Group (ECOG) performance status ≥ 1, AFP > 400 ng/mL, Albumin-Bilirubin (ALBI) grade 3, and vascular invasion were significantly associated with reduced OS ( p < 0.05). Patients who achieved partial response or stable disease per RECIST were more likely to continue Sorafenib beyond 6 months. Toxicity was generally tolerable, with a low rate of permanent treatment discontinuation. Conclusion Sorafenib continues to demonstrate efficacy in real-world practice as first-line therapy for advanced HCC, with clear clinical and biochemical indicators, including ALBI grade, AFP, ECOG, and early radiological response, serving as key prognostic factors of treatment success. Early response assessment with identification of poor prognostic factors is critical for optimizing outcomes, and proactive toxicity management can improve outcomes in real-world settings.

Future Journal of Pharmaceutical SciencesVol. 11(1)
University of Sadat City (EG), Menoufia University (EG), Assiut University (EG)
Openalex Percentile: Top 15%
Hepatocellular Carcinoma Treatment and Prognosis
1.32
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