Cabazitaxel is a taxoid synthesized from 10-deacetylbaccatin III, a compound isolated from the yew tree. As a second-generation semisynthetic microtubule inhibitor, cabazitaxel stabilizes microtubules and induces tumour cell death. Due to its low affinity for the P-glycoprotein (P-gp) efflux pump, cabazitaxel can more readily penetrate the blood–brain barrier compared to other taxanes like paclitaxel and docetaxel.
Cabazitaxel is used to treat metastatic castration-resistant prostate cancer. It was first approved by the FDA on June 17, 2010. It was also approved by the EMA on March 17, 2011 and Health Canada on December 17, 2019.
用于治疗转移性去势抵抗性前列腺癌患者。
Duke University Medical Center, Durham, North Carolina, United States
MD Anderson Cancer Center, Houston, Texas, United States
M D Anderson Cancer Center, Houston, Texas, United States
Research Site, Madrid, Spain
Thomas Jeferson University, Philadelphia, Pennsylvania, United States
Masonic Cancer Center at University of Minnesota, Minneapolis, Minnesota, United States
University of Chicago, Chicago, Illinois, United States
Akershus Universitetssykehus, Lørenskog, Norway
OLV Ziekenhuis Aalst, Aalst, Belgium
Ziekenhuis Oost-Limburg, Genk, Belgium
OHSU Knight Cancer Institute, Portland, Oregon, United States
Centre Hospitalier de l'Université de Montréal, Montréal, Quebec, Canada
Bayer US, Whippany, New Jersey, United States
Johns Hopkins University/Sidney Kimmel Cancer Center, Baltimore, Maryland, United States
Richard L. Roudebush Veterans Affairs Medical Center, Indianapolis, Indiana, United States
Sidney and Lois Eskenazi Hospital, Indianapolis, Indiana, United States
Stay informed with timely notifications on clinical trials, regulatory changes, and research advancements related to this medication.