TY - JOUR
T1 - Epothilones
T2 - Mechanism of action and biologic activity
AU - Goodin, Susan
AU - Kane, Michael P.
AU - Rubin, Eric H.
PY - 2004
Y1 - 2004
N2 - Drugs that target microtubules are among the most commonly prescribed anticancer therapies. Although the mechanisms by which perturbation of microtubule function leads to selective death of cancer cells remain unclear, several new microtubule-targeting compounds are undergoing clinical testing. In part, these efforts focus on overcoming some of the problems associated with taxane-based therapies, including formulation and administration difficulties and susceptibility to resistance conferred by P-glycoprotein. Epothilones have emerged from these efforts as a promising new class of anticancer drugs. Preclinical studies indicate that epothilones bind to and stabilize microtubules in a manner similar but not identical to that of paclitaxel and that epothilones are effective in paclitaxel-resistant tumor models. Clinical phase I and early phase II data are available for BMS-247550, BMS-310705, EPO906, and KOS-862. The results suggest that these compounds have a broad range of antitumor activity at doses and schedules associated with tolerable side effects.
AB - Drugs that target microtubules are among the most commonly prescribed anticancer therapies. Although the mechanisms by which perturbation of microtubule function leads to selective death of cancer cells remain unclear, several new microtubule-targeting compounds are undergoing clinical testing. In part, these efforts focus on overcoming some of the problems associated with taxane-based therapies, including formulation and administration difficulties and susceptibility to resistance conferred by P-glycoprotein. Epothilones have emerged from these efforts as a promising new class of anticancer drugs. Preclinical studies indicate that epothilones bind to and stabilize microtubules in a manner similar but not identical to that of paclitaxel and that epothilones are effective in paclitaxel-resistant tumor models. Clinical phase I and early phase II data are available for BMS-247550, BMS-310705, EPO906, and KOS-862. The results suggest that these compounds have a broad range of antitumor activity at doses and schedules associated with tolerable side effects.
UR - http://www.scopus.com/inward/record.url?scp=3042701597&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=3042701597&partnerID=8YFLogxK
U2 - 10.1200/JCO.2004.12.001
DO - 10.1200/JCO.2004.12.001
M3 - Review article
C2 - 15143095
AN - SCOPUS:3042701597
SN - 0732-183X
VL - 22
SP - 2015
EP - 2025
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 10
ER -