Combretastatin A-4 and hyperthermia; a potent combination for the treatment of solid tumors

Background and purpose: Attacking tumor vasculature is a promising approach for the treatment of solid tumors. The tubulin inhibitor combretastatin A- 4 disodium phosphate (CA-4) is a new vascular targeting drug which displays a low toxicity profile. We wanted to investigate how CA-4 influences tumor perfusion in the BT(4)An rat glioma and how the vascular targeting propert ies of CA-4 could be exploited to augment hyperthermic damage towards tumor vasculature. Material and methods: We used the (RbCl)-Rb-86 extraction technique to asse ss how CA-4 influences tumor perfusion, and the tumor endothelium was exami ned for morphological changes induced by the drug. We combined CA-4 (50 mg/ kg i.p.) with hyperthermia (44 degreesC, 60 min) at different time interval s to evaluate how therapy should be designed to affect tumor growth, and we studied the tumors histologically to assess tissue viability. Results: We found that CA-4 induced a profound, but transient reduction in tumor perfusion 3-6 h postinjection. If hyperthermia was administered 3-6 h after injecting CA-4, massive hemorrhagic necrosis developed, and tumor re sponse was significantly enhanced compared to simultaneous administration o f the two treatment modalities (P<0.005). CA-4 alone had no influence on tu mor growth and failed to disrupt the vasculature of the BT(4)An solid tumor s. Interestingly though, a mild endothelial edema was observed in some tumo r areas 3 h after injecting CA-4. Conclusions: We conclude that the combination of CA-4 and hyperthermia is a potent therapeutic option for BT(4)An tumors, but the selection of adequat e time intervals between CA-4 and hyperthermia are imperative to obtain tum or response. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.