Pharmacokinetic drug-drug interactions: an insight into recent US FDA-approved drugs for prostate cancer

被引:7
|
作者
Gajula, Siva Nageswara Rao [1 ]
Reddy, Gangireddy Navitha [1 ]
Reddy, Dannarm Srinivas [1 ]
Sonti, Rajesh [1 ]
机构
[1] Natl Inst Pharmaceut Educ & Res NIPER, Dept Pharmaceut Anal, Balanagar 500037, Telangana, India
关键词
combination therapy; CYP enzymes; drug– drug interactions; prostate cancer; transporters; ACETATE PLUS PREDNISONE; ABIRATERONE ACETATE; IN-VITRO; P-GLYCOPROTEIN; ANDROGEN RECEPTOR; CYTOCHROME-P450; ENZYMES; MEMBRANE TRANSPORTERS; INCREASED SURVIVAL; ENZALUTAMIDE; DOCETAXEL;
D O I
10.4155/bio-2020-0242
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Pharmacokinetic drug-drug interaction is a significant safety and efficiency concern as it results in considerable concentration changes. Drug-drug interactions are a substantial concern in anticancer drugs that possess a narrow therapeutic index. These interactions remain as the principal regulatory obstacle that can lead to termination in the preclinical stage, restrictions in the prescription, dosage adjustments or withdrawal of the drugs from the market. Drug metabolizing enzymes or transporters mediate the majority of clinically relevant drug interactions. Cancer diagnosed aged patients use multiple medications and are more prone to significant drug-drug interactions. This review provides detailed information on clinically relevant drug-drug interactions resulting from drug metabolism by enzymes and transporters with a particular emphasis on recent FDA approved antiprostate cancer drugs.
引用
收藏
页码:1647 / 1664
页数:18
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