Saponara Maristella, Gatto Lidia, Di Nunno Vincenzo, Tabacchi Elena, Fanti Stefano, Di Scioscio Valerio, Nannini Margherita, Gruppioni Elisa, Altimari Annalisa, Fiorentino Michelangelo, Santini Donatella, Ceccarelli Claudio, Zompatori Maurizio, Biasco Guido, Pantaleo Maria Abbondanza
aDepartment of Specialized, Experimental, and Diagnostic Medicine bNuclear Medicine Unit, Department of Specialized, Experimental, and Diagnostic Medicine cCardio-thoracic Radiology Unit, Department of Specialized, Experimental, and Diagnostic Medicine dDepartment of Pathology, Laboratory of Oncologic and Transplantation Molecular Pathology ePathology Unit, Department of Specialized, Experimental, and Diagnostic Medicine, Sant'Orsola-Malpighi Hospital fInterdepartmental Centre of Cancer Research 'G. Prodi', University of Bologna, Bologna, Italy.
Anticancer Drugs. 2016 Apr;27(4):353-63. doi: 10.1097/CAD.0000000000000331.
Imatinib is the standard first-line therapy for metastatic gastrointestinal stromal tumors. It has markedly improved the prognosis and outcome of patients affected by gastrointestinal stromal tumors, especially in the case of exon 11 KIT mutations. Imatinib-associated adverse events are generally mild to moderate; however, in clinical practice, intolerance caused by chronic toxicities frequently leads to breaks in treatment. This is particularly true in elderly patients in whom age, decline in drug metabolism, and polypharmacy, with a possible drug-drug interaction, may influence the tolerability of imatinib. In the present article, we report our extensive experience with the management of imatinib therapy in a 'real' population, in particular in very elderly patients, discussing whether the use of personalized imatinib dosage could be a safe and advantageous option, enabling continuous administration, thus ensuring effective treatment. Only a few case reports in the literature provide data on outcome with low tailored dosage of imatinib and none of them has been carried out on a Western population. Here, we report four cases treated with low imatinib dosage as a safe and useful option enabling continued treatment with imatinib, improving tolerance, and maintaining good and lasting disease control.
伊马替尼是转移性胃肠道间质瘤的标准一线治疗药物。它显著改善了胃肠道间质瘤患者的预后和治疗结果,尤其是在第11外显子KIT基因突变的情况下。伊马替尼相关的不良事件一般为轻至中度;然而,在临床实践中,慢性毒性导致的不耐受经常导致治疗中断。在老年患者中尤其如此,年龄、药物代谢能力下降以及多种药物联合使用(可能存在药物相互作用)可能会影响伊马替尼的耐受性。在本文中,我们报告了我们在“真实”人群中管理伊马替尼治疗的广泛经验,特别是在高龄患者中,讨论使用个性化伊马替尼剂量是否可能是一种安全且有益的选择,能够实现持续给药,从而确保有效治疗。文献中仅有少数病例报告提供了低剂量定制伊马替尼治疗结果的数据,且均未在西方人群中开展。在此,我们报告4例接受低剂量伊马替尼治疗的病例,该治疗作为一种安全且有用的选择,能够继续使用伊马替尼治疗,提高耐受性,并维持良好且持久的疾病控制。