Department of Pediatrics, Schulich School of Medicine and Dentistry, Western University, London, Ontario N6A 3M7, Canada; email:
Division of Translational Therapeutics, Department of Pediatrics, University of British Columbia, Vancouver, British Columbia V5Z 4H4, Canada.
Annu Rev Pharmacol Toxicol. 2021 Jan 6;61:679-699. doi: 10.1146/annurev-pharmtox-031320-104151. Epub 2020 Sep 25.
Cancer is the leading cause of death in American children older than 1 year of age. Major developments in drugs such as thiopurines and optimization in clinical trial protocols for treating cancer in children have led to a remarkable improvement in survival, from approximately 30% in the 1960s to more than 80% today. Short-term and long-term adverse effects of chemotherapy still affect most survivors of childhood cancer. Pharmacogenetics plays a major role in predicting the safety of cancer chemotherapy and, in the future, its effectiveness. Treatment failure in childhood cancer-due to either serious adverse effects that limit therapy or the failure of conventional dosing to induce remission-warrants development of new strategies for treatment. Here, we summarize the current knowledge of the pharmacogenomics of cancer drug treatment in children and of statistically and clinically relevant drug-gene associations and the mechanistic understandings that underscore their therapeutic value in the treatment of childhood cancer.
癌症是 1 岁以上美国儿童死亡的主要原因。噻唑嘌呤类药物等方面的重大进展,以及儿童癌症治疗临床试验方案的优化,使得儿童癌症的生存率显著提高,从 20 世纪 60 年代的约 30%提高到今天的 80%以上。化疗的短期和长期不良反应仍影响大多数儿童癌症幸存者。药物遗传学在预测癌症化疗的安全性方面发挥着重要作用,在未来,还将预测其有效性。由于严重的不良反应限制了治疗,或常规剂量未能诱导缓解,导致儿童癌症的治疗失败,这就需要制定新的治疗策略。在这里,我们总结了儿童癌症药物治疗的药物基因组学的现有知识,以及具有统计学和临床相关性的药物-基因关联,以及强调其在儿童癌症治疗中的治疗价值的机制理解。