Milhem Mohammed, Deutsch Jeremy M
Department of Hematology and Oncology, C 32 GH, University of Iowa Hospitals and Clinics, Iowa City, IA 52242, USA.
Curr Clin Pharmacol. 2015;10(4):311-20. doi: 10.2174/1574884710666151020100518.
Imatinib therapy has revolutionized the treatment of patients with gastrointestinal stromal tumors (GISTs). Compared with older therapy, imatinib significantly improves outcomes in patients with metastatic disease and those with locally advanced tumors, raising progression-free and overall survival. Recent studies have evaluated variables such as timing of treatment, total dosing, and duration of therapy. Different genotypes are associated with a poorer response to imatinib therapy, whereas others may benefit from a higher starting dose. This review discusses recent data regarding optimal use of imatinib for treatment of GIST in both the adjuvant and metastatic settings, and addresses topics such as the impact of genotype on initial dose, dose escalation, optimal duration of treatment, and neoadjuvant therapy. Key ongoing clinical trials of imatinib in GIST are also discussed.
伊马替尼治疗彻底改变了胃肠道间质瘤(GIST)患者的治疗方式。与传统治疗相比,伊马替尼显著改善了转移性疾病患者和局部晚期肿瘤患者的治疗效果,提高了无进展生存期和总生存期。最近的研究评估了治疗时机、总剂量和治疗持续时间等变量。不同的基因型与对伊马替尼治疗的反应较差相关,而其他一些基因型可能从更高的起始剂量中获益。本综述讨论了关于伊马替尼在辅助和转移性治疗中治疗GIST的最佳使用的最新数据,并探讨了基因型对初始剂量、剂量递增、最佳治疗持续时间和新辅助治疗的影响等主题。还讨论了伊马替尼在GIST方面正在进行的关键临床试验。