紫杉烷
卡巴齐塔塞尔
紫杉醇
药理学
抗药性
前列腺癌
医学
药品
多西紫杉醇
肿瘤科
癌症
内科学
生物
乳腺癌
雄激素剥夺疗法
微生物学
作者
Yu Chen,Yue Pan,Danrong Hu,Jinrong Peng,Ying Hao,Meng Pan,Liping Yuan,Jing Wang,Zhiyong Qian
标识
DOI:10.1088/1748-605x/abe396
摘要
Abstract The antitumor efficacy of various paclitaxel (PTX) and docetaxel (DTX) formulations in clinical applications is seriously affected by drug resistance. Cabazitaxel, a second-generation taxane, exhibits greater anticancer activity than PTX and DTX and has low affinity for the P-glycoprotein efflux pump because of its structure. Therefore, cabazitaxel has the potential to overcome taxane resistance. However, owing to the high systemic toxicity and hydrophobicity of cabazitaxel and the instability of its commercial preparation, Jevtana®, the clinical use of cabazitaxel is restricted to patients with metastatic castration-resistant prostate cancer who show progression after DTX-based chemotherapy. Nanomedicine is expected to overcome the limitations associated with cabazitaxel application and surmount taxane resistance. This review outlines the drug delivery systems of cabazitaxel published in recent years, summarizes the challenges faced in the development of cabazitaxel nanoformulations, and proposes strategies to overcome these challenges.
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