Almási M, Sevcíková S, Sváhová H, Sábláková B, Májková P, Hájek R
Laboratory of Experimental Hematology and Cell Immunotherapy, Department of Clinical Hematology, University Hospital Brno, Czech Republic.
Klin Onkol. 2011;24 Suppl:S39-42.
The introduction of new drugs improved clinical response of patients with diagnosed multiple myeloma (MM); however, MM is still an incurable disease that leads to frequent relapses. Individual genetic variability can significantly affect therapeutic response, sensitivity and toxicity. Analysis of single nucleotide polymorphisms (SNPs) to study genetic changes is the genomic method that can obtain information for improving the effectiveness of treatment with minimum undesirable toxicity followed by individual treatments. The aim of this paper is to explain the possibility of detection and evaluation of polymorphisms associated with toxicity of treatment in patients with MM.
新药的引入改善了已确诊多发性骨髓瘤(MM)患者的临床反应;然而,MM仍然是一种无法治愈的疾病,会导致频繁复发。个体遗传变异性会显著影响治疗反应、敏感性和毒性。分析单核苷酸多态性(SNP)以研究基因变化是一种基因组方法,该方法能够获取信息以提高治疗效果,同时将不良毒性降至最低,进而实现个体化治疗。本文旨在解释检测和评估与MM患者治疗毒性相关多态性的可能性。