TY - JOUR
T1 - Mifepristone
T2 - Antineoplastic studies
AU - Sartor, Oliver
AU - Figg, William D.
PY - 1996
Y1 - 1996
N2 - Emerging research suggests that mifepristone may have significant clinical applications in the treatment of certain neoplastic disorders. For example, in vitro studies have shown that RU-486 can inhibit or stimulate--depending on the cell line and the hormonal milieu of the culture medium--the growth of breast cancer cells. In hormone-sensitive breast cancer, anti-tumor activity is maximized by treatment with a combination of RU-486 and estrogen antagonists such as tamoxifen or luteinizing hormone releasing hormone analogues. The few studies of RU-486 administration in women with advanced breast cancer that had failed to respond to tamoxifen have demonstrated short-term disease stabilization (e.g., 5-10 months). This research has suggested that progesterone receptors are necessary but not sufficient for anti-tumor responses. Also promising, although untested in a large-scale study, is use of RU-486 in women with progressive recurrent and/or unresectable benign meningiomas. In addition, RU-486 has inhibited hormone-insensitive human prostate cancer cell lines grown in vitro and in nude mice xenografts.
AB - Emerging research suggests that mifepristone may have significant clinical applications in the treatment of certain neoplastic disorders. For example, in vitro studies have shown that RU-486 can inhibit or stimulate--depending on the cell line and the hormonal milieu of the culture medium--the growth of breast cancer cells. In hormone-sensitive breast cancer, anti-tumor activity is maximized by treatment with a combination of RU-486 and estrogen antagonists such as tamoxifen or luteinizing hormone releasing hormone analogues. The few studies of RU-486 administration in women with advanced breast cancer that had failed to respond to tamoxifen have demonstrated short-term disease stabilization (e.g., 5-10 months). This research has suggested that progesterone receptors are necessary but not sufficient for anti-tumor responses. Also promising, although untested in a large-scale study, is use of RU-486 in women with progressive recurrent and/or unresectable benign meningiomas. In addition, RU-486 has inhibited hormone-insensitive human prostate cancer cell lines grown in vitro and in nude mice xenografts.
UR - http://www.scopus.com/inward/record.url?scp=0029882238&partnerID=8YFLogxK
U2 - 10.1097/00003081-199606000-00023
DO - 10.1097/00003081-199606000-00023
M3 - Review article
C2 - 8734014
AN - SCOPUS:0029882238
SN - 0009-9201
VL - 39
SP - 498
EP - 505
JO - Clinical Obstetrics and Gynecology
JF - Clinical Obstetrics and Gynecology
IS - 2
ER -