Pharmacokinetics of metronomic chemotherapy: a neglected but crucial aspect

被引:159
作者
Bocci, Guido [1 ]
Kerbel, Robert S. [2 ,3 ]
机构
[1] Univ Pisa, Div Farmacol, Dipartimento Med Clin & Sperimentale, Via Roma 55, I-56126 Pisa, Italy
[2] Odette Canc Ctr, Sunnybrook Res Inst, Biol Sci Platform, S-217,2075 Bayview Ave, Toronto, ON M4N 3M5, Canada
[3] Univ Toronto, Dept Med Biophys, S-217,2075 Bayview Ave, Toronto, ON M4N 3M5, Canada
关键词
BREAST-CANCER PATIENTS; ANTITUMOR INNATE IMMUNITY; RANDOMIZED PHASE-II; ORAL TOPOTECAN; IN-VITRO; ANTICANCER DRUGS; CYCLOPHOSPHAMIDE TREATMENT; CLINICAL PHARMACOKINETICS; ANTIANGIOGENIC ACTIVITY; DOSE CHEMOTHERAPY;
D O I
10.1038/nrclinonc.2016.64
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Metronomic chemotherapy describes the close, regular administration of chemotherapy drugs at less-toxic doses over prolonged periods of time. In 2015, the results of randomized phase III clinical trials demonstrated encouraging, albeit limited, efficacy benefits of metronomic chemotherapy regimens administered as adjuvant maintenance therapy for the treatment of breast cancer, or as maintenance therapy in combination with an antiangiogenic agent for metastatic colorectal cancer. Owing to the investigational nature of this approach, metronomic chemotherapy regimens are highly empirical in terms of the optimal dose and schedule for the drugs administered; therefore, greater knowledge of the pharmacokinetics of metronomic chemotherapy is critical to the future success of this treatment strategy. Unfortunately, such preclinical and clinical pharmacokinetic studies are rare. Herein, we present situations in which active drug concentrations have been achieved with metronomic schedules, and discuss their associated pharmacokinetic parameters. We summarize examples from the limited number of clinical studies in order to illustrate the importance of assessing such pharmacokinetic parameters, and discuss the influence this information can have on improving efficacy and reducing toxicity.
引用
收藏
页码:659 / 673
页数:15
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