伊立替康剂量和药物基因组学:基于 UGT1A1 变异和新见解的全面探索。

IF 1.9 4区 医学 Q3 INFECTIOUS DISEASES Journal of Chemotherapy Pub Date : 2024-05-06 DOI:10.1080/1120009X.2024.2349444
Muhammad Saleem Faisal, Imran Hussain, Muhammad Abdullah Ikram, Syed Babar Shah, Abdul Rehman, Wajid Iqbal
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引用次数: 0

摘要

伊立替康是一种重要的抗癌药物,通过阻碍拓扑异构酶 1 来治疗转移性结直肠癌和晚期胰腺导管腺癌。UDP 葡萄糖醛酸转移酶家族 1 成员 A1(UGT1A1)多态性会增加伊立替康诱发中性粒细胞减少症和腹泻的风险。因此,建议在以伊立替康为基础的化疗前筛查 UGT1A1 多态性,以尽量减少毒性,而脂质体则有可能在胰腺导管腺癌患者中以较少的副作用给药伊立替康。本综述全面概述了在基因型指导下服用伊立替康对 UGT1A1*28 和 UGT1A1*6 变异的影响,并结合了药物基因组学研究、使用伊立替康治疗转移性结直肠癌和胰腺癌的最佳方案、减少毒性的指导原则以及 UGT1A1 基因型检测的成本效益评估。
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Irinotecan dosing and pharmacogenomics: a comprehensive exploration based on UGT1A1 variants and emerging insights.

Irinotecan is a critical anticancer drug used to treat metastatic colorectal cancer and advanced pancreatic ductal adenocarcinoma by obstructing topoisomerase 1; however, it can cause minor-to-severe and life-threatening adverse effects. UDP glucuronosyltransferase family 1 member A1 (UGT1A1) polymorphisms increase the risk of irinotecan-induced neutropenia and diarrhea. Hence, screening for UGT1A1 polymorphisms before irinotecan-based chemotherapy is recommended to minimize toxicity, whereas liposomes offer the potential to deliver irinotecan with fewer side effects in patients with pancreatic ductal adenocarcinoma. This review presents a comprehensive overview of the effects of genotype-guided dosing of irinotecan on UGT1A1*28 and UGT1A1*6 variants, incorporating pharmacogenomic research, optimal regimens for metastatic colorectal and pancreatic cancer treatment using irinotecan, guidelines for toxicity reduction, and an evaluation of the cost-effectiveness of UGT1A1 genotype testing.

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来源期刊
Journal of Chemotherapy
Journal of Chemotherapy 医学-药学
CiteScore
3.70
自引率
0.00%
发文量
144
审稿时长
6-12 weeks
期刊介绍: The Journal of Chemotherapy is an international multidisciplinary journal committed to the rapid publication of high quality, peer-reviewed, original research on all aspects of antimicrobial and antitumor chemotherapy. The Journal publishes original experimental and clinical research articles, state-of-the-art reviews, brief communications and letters on all aspects of chemotherapy, providing coverage of the pathogenesis, diagnosis, treatment, and control of infection, as well as the use of anticancer and immunomodulating drugs. Specific areas of focus include, but are not limited to: · Antibacterial, antiviral, antifungal, antiparasitic, and antiprotozoal agents; · Anticancer classical and targeted chemotherapeutic agents, biological agents, hormonal drugs, immunomodulatory drugs, cell therapy and gene therapy; · Pharmacokinetic and pharmacodynamic properties of antimicrobial and anticancer agents; · The efficacy, safety and toxicology profiles of antimicrobial and anticancer drugs; · Drug interactions in single or combined applications; · Drug resistance to antimicrobial and anticancer drugs; · Research and development of novel antimicrobial and anticancer drugs, including preclinical, translational and clinical research; · Biomarkers of sensitivity and/or resistance for antimicrobial and anticancer drugs; · Pharmacogenetics and pharmacogenomics; · Precision medicine in infectious disease therapy and in cancer therapy; · Pharmacoeconomics of antimicrobial and anticancer therapies and the implications to patients, health services, and the pharmaceutical industry.
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