Current status of angiogenesis inhibitors combined with radiation therapy

被引:114
作者
Nieder, Carsten
Wiedenmann, Nicole
Andratschke, Nicolaus
Molls, Michael
机构
[1] Tech Univ Munich, Klinikum Rechts Isar, Dept Radiat Oncol, D-81675 Munich, Germany
[2] Univ Texas, MD Anderson Canc Ctr, Dept Expt Radiat Oncol, Houston, TX 77030 USA
关键词
radiotherapy; cancer; angiogenesis; radiosensitizer; vascular endothelial growth factor;
D O I
10.1016/j.ctrv.2006.03.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Angiogenesis inhibitors combined with cytotoxic chemotherapy have recently entered routine oncological practice. Several rationales exist for combining these agents with ionizing radiation, a primary curative cancer treatment, either in bimodal or trimodal fashion, i.e. with or without additional chemotherapy. More than 20 different anti-angiogenic agents have been studied in preclinical animal tumor models. This systematic review compares the results of preclinical studies published before February 2006. The combination of vascular endothelial growth factor (VEGF) inhibitors with irradiation consistently resulted in improved tumor growth delay (at least additive effects), despite different radiation schedules, drugs and doses, and combination regimens. Only two studies evaluated tumor control dose (TCD)50 as a measure of tumor cure (radiation dose yielding permanent local control in 50% of the tumors). While anti-VEGF receptor (VEGFR) antibody treatment improved the outcome, a VEGFR tyrosine kinase inhibitor showed negative results. For agents interfering with other pathways, the results are also not consistent, although most studies were positive. Trimodal approaches seem to improve tumor growth delay even further. Importantly, both radiotherapy schedule and sequence of the modalities in combined treatment may impact on the outcome. Hence, further preclinical studies examining these parameters need to be conducted. White preclinical research is ongoing, phase I and II clinical trials with bevacizumab, combretastatin A-4, thatidomide and different receptor tyrosine kinase inhibitors, usually combined with radio- and chemotherapy, have been designed. Early results suggest that acute toxicity is acceptable, planned surgery after such treatment is feasible, and that further evaluation of such combined modality treatment is warranted. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:348 / 364
页数:17
相关论文
共 105 条
[1]
Abdollahi A, 2003, CANCER RES, V63, P3755
[2]
SUPPRESSION OF RETINAL NEOVASCULARIZATION IN-VIVO BY INHIBITION OF VASCULAR ENDOTHELIAL GROWTH-FACTOR (VEGF) USING SOLUBLE VEGF-RECEPTOR CHIMERIC PROTEINS [J].
AIELLO, LP ;
PIERCE, EA ;
FOLEY, ED ;
TAKAGI, H ;
CHEN, H ;
RIDDLE, L ;
FERRARA, N ;
KING, GL ;
SMITH, LEH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (23) :10457-10461
[3]
Potential role of growth factors in diminishing radiation therapy neural tissue injury [J].
Andratschke, NH ;
Nieder, C ;
Price, RE ;
Rivera, B ;
Ang, KK .
SEMINARS IN ONCOLOGY, 2005, 32 (02) :S67-S70
[4]
Modulation of rodent spinal cord radiation tolerance by administration of platelet-derived growth factor [J].
Andratschke, NH ;
Nieder, C ;
Price, RE ;
Rivera, B ;
Tucker, SL ;
Ang, KK .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2004, 60 (04) :1257-1263
[5]
Ansiaux R, 2005, CLIN CANCER RES, V11, P743
[6]
MIGRATION AND PROLIFERATION OF ENDOTHELIAL CELLS IN PREFORMED AND NEWLY FORMED BLOOD-VESSELS DURING TUMOR ANGIOGENESIS [J].
AUSPRUNK, DH ;
FOLKMAN, J .
MICROVASCULAR RESEARCH, 1977, 14 (01) :53-65
[7]
Borgstrom P, 1996, CANCER RES, V56, P4032
[8]
Brieger J, 2005, INT J MOL MED, V15, P145
[9]
Bruns CJ, 2000, CANCER, V89, P488, DOI 10.1002/1097-0142(20000801)89:3<488::AID-CNCR3>3.3.CO
[10]
2-O