Clinical concepts for cabazitaxel in the management of metastatic castration-resistant prostate cancer

被引:16
作者
Al-Mansouri, Loma [1 ]
Gurney, Howard [1 ,2 ]
机构
[1] Macquarie Univ, Fac Med & Hlth Sci, Dept Med Oncol & Clin Trials, Sydney, NSW, Australia
[2] Westmead Hosp, Crown Princess Mary Canc Ctr, Westmead, NSW, Australia
关键词
cabazitaxel; chemotherapy naive; duration of treatment; metastatic castration-resistant prostate cancer; number of cycles; reduced dose; sequence of therapy; QUALITY-OF-LIFE; EARLY-ACCESS PROGRAM; EVERY; 3; WEEKS; ABIRATERONE ACETATE; ANTITUMOR-ACTIVITY; PLUS PREDNISONE; SAFETY DATA; OPEN-LABEL; PHASE-III; DOCETAXEL;
D O I
10.1111/ajco.13193
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Prostate cancer is the most common malignancy in male patients. The second-generation taxanes, cabazitaxel, is a therapeutic option with an overall survival advantage for patients with metastatic castration-resistant prostate cancer. This review explores specific aspects of cabazitaxel including the duration of treatment, the efficacy of lower dose and effect on the incidence of adverse effects, and optimal sequencing of cabazitaxel. A systematic search of data baselines "PubMed, Ovid Medline, Scopus, and Embase" was carried out using the keywords "cabazitaxel" and "metastatic prostate cancer." The search was limited to clinical studies performed after October 2010 addressing duration of treatment, the efficacy of lower dose, adverse effects, the sequence of cabazitaxel in relation to other lines of therapy and use in chemotherapy naive patients. The current evidence supports the utility and safety of cabazitaxel as either a second- or third-line agent after docetaxel, or as an alternative to docetaxel in the chemotherapy-naive setting. Extended duration of cabazitaxel beyond 10 cycles is feasible and does not appear to lead to cumulative toxicity. In conclusion, cabazitaxel can improve survival in castrate-resistant prostate cancer with an acceptable risk of toxicity. Studies confirmed the efficacy of reduced dose and utility in patients without prior chemotherapy.
引用
收藏
页码:288 / 295
页数:8
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