期刊文献+

Optimal combination of antiangiogenic therapy for hepatocellular carcinoma 被引量:4

Optimal combination of antiangiogenic therapy for hepatocellular carcinoma
下载PDF
导出
摘要 The success of sorafenib in prolonging survival of patients with hepatocellular carcinoma(HCC) makes therapeutic inhibition of angiogenesis a component of treatment for HCC. To enhance therapeutic efficacy, overcomedrug resistance and reduce toxicity, combination of antiangiogenic agents with chemotherapy, radiotherapy or other targeted agents were evaluated. Nevertheless, the use of antiangiogenic therapy remains suboptimal regarding dosage, schedule and duration of therapy. The issue is further complicated by combination antiangiogenesis to other cytotoxic or biologic agents. There is no way to determine which patients are most likely respond to a given form of antiangiogenic therapy. Activation of alternative pathways associated with disease progression in patients undergoing antiangiogenic therapy has also been recognized. There is increasing importance in identifying, validating and standardizing potential response biomarkers for antiangiogenesis therapy for HCC patients. In this review, biomarkers for antiangiogenesis therapy including systemic, circulating, tissue and imaging ones are summarized. The strength and deficit of circulating and imaging biomarkers were further demonstrated by a series of studies in HCC patients receiving radiotherapy with or without thalidomide. The success of sorafenib in prolonging survival of patientswith hepatocellular carcinoma (HCC) makes therapeuticinhibition of angiogenesis a component of treatmentfor HCC. To enhance therapeutic efficacy, overcome drug resistance and reduce toxicity, combination ofantiangiogenic agents with chemotherapy,radiotherapyor other targeted agents were evaluated. Nevertheless,the use of antiangiogenic therapy remains suboptimalregarding dosage, schedule and duration of therapy.The issue is further complicated by combinationantiangiogenesis to other cytotoxic or biologic agents.There is no way to determine which patients are mostlikely respond to a given form of antiangiogenic therapy.Activation of alternative pathways associated with diseaseprogression in patients undergoing antiangiogenictherapy has also been recognized. There is increasingimportance in identifying, validating and standardizingpotential response biomarkers for antiangiogenesistherapy for HCC patients. In this review, biomarkers forantiangiogenesis therapy including systemic, circulating,tissue and imaging ones are summarized. The strengthand deficit of circulating and imaging biomarkerswere further demonstrated by a series of studies inHCC patients receiving radiotherapy with or withoutthalidomide.
作者 Hui-Ju Ch'ang
出处 《World Journal of Hepatology》 CAS 2015年第16期2029-2040,共12页 世界肝病学杂志(英文版)(电子版)
基金 Supported by National Health Research Institutes,Taiwan
关键词 ANTIANGIOGENESIS HEPATOCELLULAR carcinoma BIOMARKER CYTOKINES Dynamic CONTRAST enhancedmagnetic RESONANCE imaging Antiangiogenesis Hepatocellular carcinoma Biomarker Cytokines Dynamic contrast enhanced magnetic resonance imaging
  • 相关文献

参考文献1

二级参考文献25

  • 1[1]Burroughs A,Hochhauser D,Meyer T.Systemic treatment and liver transplantation for hepatocellular carcinoma:two ends of the therapeutic spectrum.Lancet Oncol 2004; 5:409-418
  • 2[2]Llovet JM,Burroughs A,Bruix J.Hepatocellular carcinoma.Lancet 2003; 362:1907-1917
  • 3[3]Torimura T,Sata M,Ueno T,Kin M,Tsuji R,Suzaku K,Hashimoto O,Sugawara H,Tanikawa K.Increased expression of vascular endothelial growth factor is associated with tumor progression in hepatocellular carcinoma.Hum Pathol 1998; 29:986-991
  • 4[4]Yamaguchi R,Yano H,Iemura A,Ogasawara S,Haramaki M,Kojiro M.Expression of vascular endothelial growth factor in human hepatocellular carcinoma.Hepatology 1998; 28:68-77
  • 5[5]Kenyon BM,Browne F,D'Amato RJ.Effects of thalidomide and related metabolites in a mouse corneal model of neovascularization.Exp Eye Res 1997; 64:971-978
  • 6[6]Peuckmann V,Fisch M,Bruera E.Potential novel uses of thalidomide:focus on palliative care.Drugs 2000; 60:273-292
  • 7[7]Little RF,Wyvill KM,Pluda JM,Welles L,Marshall V,Figg WD,Newcomb FM,Tosato G,Feigal E,Steinberg SM,Whitby D,Goedert JJ,Yarchoan R.Activity of thalidomide in AIDS-related Kaposi's sarcoma.J Clin Oncol 2000; 18:2593-2602
  • 8[8]Patterson SG,Fishman M,Kish J,Ewbank D,Defelice J,Rago R.Thalidomide plus daily oral dexamethasone for metastatic hormone refractory prostate cancer (HRPC) in patients previously treated with cytotoxic chemothertapy.Proc Am Soc Clin Oncol 2003; 22:444,abstract:1783
  • 9[9]Sobin L,Wittekind C.TMN classification of malignant tumours.5th ed.New York:Wiley-Liss,1997:74-77
  • 10[10]Okuda K.Early recognition of hepatocellular carcinoma.Hepatology 1986; 6:729-738

共引文献20

同被引文献15

引证文献4

二级引证文献34

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部