HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Targeting the tumor vasculature: enhancing antitumor efficacy through combination treatment with ZD6126 and ZD6474.

AbstractBACKGROUND:
The antitumor efficacy of combination therapy of the vascular disrupting agent ZD6126 and antiangiogenic agent ZD6474 was evaluated in the models of human colorectal (HT29) and ovarian carcinoma (OW1).
MATERIALS AND METHODS:
HT29 and OW1 xenograft-bearing mice were treated with ZD6126 and ZD6474 either alone or in combination. ZD6126 therapy consisted of three doses of 100 mg/kg administered 1, 3 and 5 days after the tumor reached the starting size. ZD6474 was administered daily at a dose of 25 mg/kg on days 1-5.
RESULTS:
ZD6126 and ZD6474 treatment alone only resulted in modest tumor growth delay. However, significantly enhanced antitumor effects were observed in the combination treatment.
CONCLUSION:
The combination of the vascular disrupting with the antiangiogenic agent led to significant enhancement of antitumor efficacy in HT29 and OW1 human tumor models. Such combination therapy may have significant therapeutic benefit even in tumors insensitive to either treatment alone.
AuthorsWenyin Shi, Dietmar W Siemann
JournalIn vivo (Athens, Greece) (In Vivo) 2005 Nov-Dec Vol. 19 Issue 6 Pg. 1045-50 ISSN: 0258-851X [Print] Greece
PMID16277020 (Publication Type: Comparative Study, Evaluation Study, Journal Article, Research Support, N.I.H., Extramural, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Antineoplastic Agents
  • N-acetylcochinol-O-phosphate
  • Organophosphorus Compounds
  • Piperidines
  • Quinazolines
  • vandetanib
Topics
  • Animals
  • Antineoplastic Agents (pharmacology)
  • Antineoplastic Combined Chemotherapy Protocols
  • Carcinoma (pathology)
  • Cell Line, Tumor
  • Colorectal Neoplasms (pathology, therapy)
  • Drug Evaluation, Preclinical
  • Endothelium, Vascular (pathology)
  • Female
  • HT29 Cells
  • Humans
  • Mice
  • Mice, Nude
  • Necrosis (drug therapy)
  • Neoplasm Transplantation
  • Neovascularization, Pathologic (prevention & control)
  • Organophosphorus Compounds (administration & dosage, pharmacology)
  • Ovarian Neoplasms (pathology, therapy)
  • Piperidines (administration & dosage, pharmacology)
  • Quinazolines (administration & dosage, pharmacology)
  • Survival Analysis
  • Time Factors
  • Transplantation, Heterologous
  • Tumor Burden (drug effects)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: