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Sorafenib plus transarterial chemoembolization vs sorafenib alone for patients with advanced hepatocellular carcinoma: A systematic review and meta-analysis.
Yang, Hong-Jie; Ye, Bin; Liao, Jia-Xu; Lei, Lei; Chen, Kai.
Affiliation
  • Yang HJ; Department of Radiology, The Sixth People's Hospital of Chengdu, Chengdu 610000, Sichuan Province, China.
  • Ye B; Department of Oncology, The Sixth People's Hospital of Chengdu, Chengdu 610000, Sichuan Province, China.
  • Liao JX; Department of Radiology, The Sixth People's Hospital of Chengdu, Chengdu 610000, Sichuan Province, China.
  • Lei L; Department of Oncology, The Sixth People's Hospital of Chengdu, Chengdu 610000, Sichuan Province, China.
  • Chen K; Department of Pharmacy, The Affiliated Taizhou People's Hospital of Nanjing Medical University, Taizhou 225300, Jiangsu Province, China. kaichen@njmu.edu.cn.
World J Hepatol ; 16(1): 91-102, 2024 Jan 27.
Article in En | MEDLINE | ID: mdl-38313249
ABSTRACT

BACKGROUND:

Although the past decade has seen remarkable advances in treatment options for hepatocellular carcinoma (HCC), the dismal overall prognosis still envelops HCC patients. Several comparative trials have been conducted to study whether transarterial chemoembolization (TACE) could improve clinical outcomes in patients receiving sorafenib for advanced HCC; however, the findings have been inconsistent.

AIM:

To study the potential synergies and safety of sorafenib plus TACE vs sorafenib alone for treating advanced HCC, by performing a systematic review and meta-analysis.

METHODS:

This study was conducted following the PRISMA statement. A systematic literature search was conducted using the Cochrane Library, Embase, PubMed, and Web of Science databases. Data included in the present work were collected from patients diagnosed with advanced HCC receiving sorafenib plus TACE or sorafenib alone. Data synthesis and meta-analysis were conducted using Review Manager software.

RESULTS:

The present study included 2780 patients from five comparative clinical trials (1 was randomized control trial and 4 were retrospective studies). It was found that patients receiving sorafenib plus TACE had better prognoses in terms of overall survival (OS), with a combined hazard ratio (HR) of 0.65 [95% confidence interval (95%CI) 0.46-0.93, P = 0.02, n = 2780]. Consistently, progression free survival (PFS) and time to progression (TTP) differed significantly between the sorafenib plus TACE arm and sorafenib arm (PFS HR = 0.62, 95%CI 0.40-0.96, P = 0.03, n = 443; TTP HR = 0.73, 95%CI 0.64-0.83, P < 0.00001, n = 2451). Disease control rate (DCR) was also significantly increased by combination therapy (risk ratio = 1.36, 95%CI 1.02-1.81, P = 0.04, n = 641). Regarding safety, the incidence of any adverse event (AE) was increased due to the addition of TACE; however, no significant difference was found in grade ≥ 3 AEs.

CONCLUSION:

The combination of sorafenib with TACE has superior efficacy to sorafenib monotherapy, as evidenced by prolonged OS, PFS, and TTP, as well as increased DCR. Additional high-quality trials are essential to further validate the clinical benefit of this combination in the treatment of advanced HCC.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Language: En Journal: World J Hepatol Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Language: En Journal: World J Hepatol Year: 2024 Document type: Article Affiliation country: Country of publication: