Gemcitabine plus sorafenib versus gemcitabine alone in advanced biliary tract cancer: A double-blind placebo-controlled multicentre phase II AIO study with biomarker and serum programme

被引:113
作者
Moehler, M. [1 ]
Maderer, A. [1 ]
Schimanski, C. [2 ]
Kanzler, S. [3 ]
Denzer, U. [4 ]
Kolligs, F. T. [5 ]
Ebert, M. P.
Distelrath, A. [6 ]
Geissler, M. [7 ]
Trojan, J. [8 ]
Schuetz, M. [1 ]
Berie, L. [1 ]
Sauvigny, C. [1 ]
Lammert, F. [9 ]
Lohse, A. [4 ]
Dollinger, M. M. [10 ]
Lindig, U. [11 ]
Duerr, E. M. [5 ]
Lubomierski, N. [8 ]
Zimmermann, S. [9 ]
Wachtlin, D. [12 ]
Kaiser, A. -K. [12 ]
Schadmand-Fischer, S. [13 ]
Galle, P. R. [1 ]
Woerns, M. [1 ]
机构
[1] Johannes Gutenberg Univ Mainz, Dept Internal Med, D-55131 Mainz, Germany
[2] Marienhosp Darmstadt, Dept Internal Med, Darmstadt, Germany
[3] Leopoldina Hosp, Dept Med 2, Schweinfurt, Germany
[4] Univ Hamburg Hosp, Dept Med 1, Hamburg, Germany
[5] Univ Hosp Munich, Dept Med 2, Munich, Germany
[6] Hosp Fulda, Tumor Dept, Fulda, Germany
[7] Hosp Esslingen, Dept Internal Med, Esslingen, Germany
[8] Univ Hosp Frankfurt, Dept Internal Med 1, Frankfurt, Germany
[9] Univ Hosp Homburg, Dept Internal Med 2, Homburg, Germany
[10] Univ Hosp Ulm, Dept Internal Med 1, Ulm, Germany
[11] Univ Hosp Jena, Dept Internal Med 2, Jena, Germany
[12] Univ Med Ctr, Interdisciplinary Ctr Clin Trials, Mainz, Germany
[13] Johannes Gutenberg Univ Mainz, Dept Radiol, D-55131 Mainz, Germany
关键词
Advanced biliary tract cancer; BTC; Sorafenib; Hand-foot syndrome; VEGFR-2; VEGFR-3; c-kit; PDGFR beta; Hif1; alpha; ADVANCED HEPATOCELLULAR-CARCINOMA; ENDOTHELIAL GROWTH-FACTOR; OPEN-LABEL; GALLBLADDER CARCINOMA; SKIN TOXICITY; CHOLANGIOCARCINOMA; OXALIPLATIN; COMBINATION; TRIAL; CHEMOTHERAPY;
D O I
10.1016/j.ejca.2014.09.013
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Since sorafenib has shown activity in different tumour types and gemcitabine regimens improved the outcome for biliary tract cancer (BTC) patients, we evaluated first-line gemcitabine plus sorafenib in a double-blind phase II study. Patients and methods: 102 unresectable or metastatic BTC patients with histologically proven adenocarcinoma of gallbladder or intrahepatic bile ducts, Eastern Cooperative Oncology Group (ECOG) 0-2 were randomised to gemcitabine (1000 mg/m(2) once weekly, first 7-weeks + 1-week rest followed by once 3-weeks + 1-week rest) plus sorafenib (400 mg twice daily) or placebo. Treatment continued until progression or unacceptable toxicity. Tumour samples were prospectively stained for sorafenib targets and potential biomarkers. Serum samples (first two cycles) were measured for vascular endothelial growth factors (VEGFs), vascular endothelial growth factor receptor 2 (VEGFR-2) and stromal cell-derived factor 1 (SDF1) a by enzyme-linked immunosorbent assay (ELISA). Results: Gemcitabine plus sorafenib was generally well tolerated. Four and three patients achieved partial responses in the sorafenib and placebo groups, respectively. There was no difference in the primary end-point, median progression-free survival (PFS) for gemcitabine plus sorafenib versus gemcitabine plus placebo (3.0 versus 4.9 months, P = 0.859), and no difference for median overall survival (OS) (8.4 versus 11.2 months, P = 0.775). Patients with liver metastasis after resection of primary BTC survived longer with sorafenib (P = 0.019) compared to placebo. Patients who developed hand-foot syndrome (HFS) showed longer PFS and OS than patients without HFS. Two sorafenib targets, VEGFR-2 and c-kit, were not expressed in BTC samples. VEGFR-3 and Hif1 alpha were associated with lymph node metastases and T stage. Absence of PDGFR beta expression correlated with longer PFS. Conclusion: The addition of sorafenib to gemcitabine did not demonstrate improved efficacy in advanced BTC patients. Biomarker subgroup analysis suggested that some patients might benefit from combined treatment. (C) 2014 The Authors. Published by Elsevier Ltd.
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收藏
页码:3125 / 3135
页数:11
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