Efficacy of Ramucirumab Versus Sorafenib as Subsequent Treatment for Hepatocellular Carcinoma.

Department of Gastroenterology and Hepatology, Osaka University Graduate School of Medicine, Suita, Japan. Department of Hepatobiliary and Pancreatic Oncology, Osaka International Cancer Institute, Osaka, Japan. Department of Gastroenterology and Hepatology, Osaka Police Hospital, Osaka, Japan. Department of Gastroenterology and Hepatology, Minoh City Hospital, Minoh, Japan. Department of Gastroenterology and Hepatology, Kansai Rosai Hospital, Amagasaki, Japan. Department of Gastroenterology and Hepatology, National Hospital Organization Osaka National Hospital, Osaka, Japan. Department of Gastroenterology and Hepatology, Osaka General Medical Center, Osaka, Japan. Department of Gastroenterology and Hepatology, Toyonaka Municipal Hospital, Toyonaka, Japan. Department of Gastroenterology and Hepatology, Osaka University Graduate School of Medicine, Suita, Japan; takehara@gh.med.osaka-u.ac.jp.

Anticancer research. 2021;(4):2187-2192
Full text from:

Abstract

BACKGROUND/AIM: The present study aimed to examine the therapeutic efficacy of ramucirumab compared with that of sorafenib as subsequent systemic therapy for patients with hepatocellular carcinoma (HCC) and serum α-fetoprotein (AFP) levels ≥400 ng/ml. PATIENTS AND METHODS In our prospectively registered, real-world cohort, 13 and 11 patients treated with ramucirumab or sorafenib, respectively, were analyzed. Progression-free survival (PFS) was primarily compared between the ramucirumab and sorafenib groups. RESULTS The PFS was significantly longer in the ramucirumab group than in the sorafenib group (median, 2.7 vs. 0.9 months, respectively; p=0.005). There were no significant differences in the objective response rates or the disease control rates between the ramucirumab and sorafenib groups (9.1% and 54.5% vs. 0.0% and 22.2%, respectively). CONCLUSION Subsequent systemic therapy with ramucirumab showed a better ability to control tumor progression than sorafenib in HCC patients with serum AFP levels ≥400 ng/ml.

Methodological quality

Publication Type : Clinical Trial ; Multicenter Study

Metadata