Aprepitant in the Prevention of Vomiting Induced by Moderately and Highly Emetogenic Chemotherapy

被引:5
作者
Wang, Shi-Yong [1 ]
Yang, Zhen-Jun [2 ]
Zhang, Zhe [1 ]
Zhang, Hui [1 ]
机构
[1] China Med Univ, Affiliated Hosp 4, Dept Biotherapy & Lab Biotherapy, Shenyang 110001, Peoples R China
[2] China Med Univ, Shengjing Hosp, Dept Med Informat, Shenyang 110001, Peoples R China
关键词
Neurokinin-1 receptor antagonist; aprepitant; substance P; chemotherapy-induced nausea and vomiting; ORAL NEUROKININ-1 ANTAGONIST; PLACEBO-CONTROLLED TRIAL; HIGH-DOSE CISPLATIN; INDUCED NAUSEA; DOUBLE-BLIND; RECEPTOR ANTAGONIST; NK1; ANTAGONIST; BREAST-CANCER; III TRIALS; DEXAMETHASONE;
D O I
10.7314/APJCP.2014.15.23.10045
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Chemotherapy is a major therapeutic approach for malignant neoplasms; however, due to the most common adverse events of nausea and vomiting, scheduled chemotherapeutic programs may be impeded or even interrupted, which severely impairs the efficacy. Aprepitants, 5-HT3 antagonists and dexamethasone are primary drugs used to prevent chemotherapy-induced nausea and vomiting (CINV). These drugs have excellent efficacy for control of acute vomiting but are relatively ineffective for delayed vomiting. Aprepitant may remedy this deficiency. Substance P was discovered in the 1930s and its association with vomiting was confirmed in the 1950s. This was followed by a period of non-peptide neurokinin-1 (NK-1) receptor antagonist synthesis and investigation in preclinical studies and clinical trials (phases I, II and III). The FDA granted permission for the clinical chemotherapeutic use of aprepitant in 2003. At present, the combined use of aprepitant, 5-HT3 antagonists and dexamethasone satisfactorily controls vomiting but not nausea. Therefore, new therapeutic approaches and drugs are still needed.
引用
收藏
页码:10045 / 10051
页数:7
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