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。
Investigational Site Number 410001, Seoul, Korea, Republic of
USC/Norris Comprehensive Cancer Center, Los Angeles, California, United States
National Cancer Institute, Bethesda, Maryland, United States
University of Pennsylvania, Philadelphia, Pennsylvania, United States
Thomas Jefferson University, Philadelphia, Pennsylvania, United States
Thomas Jefferson University, Philadelphia, Pennsylvania, United States
Icahn School of Medicine at Mount Sinai, New York, New York, United States
Memorial Hospital, Pawtucket, Rhode Island, United States
Brown University Oncology Research Group, Providence, Rhode Island, United States
Roger Williams, Providence, Rhode Island, United States
Medical University of South Carolina, Charleston, South Carolina, United States
Investigational Site Number 392008, Maebashi-Shi, Japan
Investigational Site Number 392015, Nagoya-Shi, Japan
Investigational Site Number 392003, Sunto-Gun, Japan
Investigational Site Number 840014, Baltimore, Maryland, United States
Investigational Site Number 840021, Stamford, Connecticut, United States
Investigational Site Number 840020, Akron, Ohio, United States
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