Clinical relevance of pharmacogenetics in gastrointestinal stromal tumor treatment in the era of personalized therapy

被引:0
作者
Angelini, Sabrina [1 ]
Ravegnini, Gloria [1 ,2 ]
Fletcher, Jonathan A. [2 ]
Maffei, Francesca [3 ]
Hrelia, Patrizia [1 ]
机构
[1] Univ Bologna, Alma Mater Studiorum, Dept Pharm & Biotechnol, I-40126 Bologna, Italy
[2] Harvard Univ, Brigham & Womens Hosp, Dept Pathol, Sch Med, Boston, MA 02115 USA
[3] Univ Bologna, Alma Mater Studiorum, Dept Life Qual Studies, I-47921 Rimini, Italy
关键词
gastrointestinal stromal tumor; imatinib; imatinib pharmacokinetics; KIT mutations; PDGFRA mutations; plasma level; EORTC-SOFT-TISSUE; TYROSINE KINASE INHIBITORS; OF-FUNCTION MUTATIONS; PHASE-II TRIAL; IMATINIB MESYLATE; ADJUVANT IMATINIB; PDGFRA MUTATIONS; GENE-EXPRESSION; DOSE IMATINIB; PLASMA-CONCENTRATIONS;
D O I
10.2217/PGS.13.63
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Gastrointestinal stromal tumor (GIST) is a well-recognized and now relatively well-understood mesenchymal tumor. Before the imatinib era, the treatment of metastatic GIST was frustrating owing to its refractoriness to conventional chemotherapy and radiotherapy. After a metastatic GIST patient was granted compassionate use of imatinib in 2000, the treatment of this disease has emerged as a model for the development of other molecularly targeted therapies. In this article the authors review how tumor genotypes, in particular KIT and PDGFRA mutational analysis, have been integrated in the optimal clinical management of GIST patients. The authors also discuss the potential practical relevance of pharmacogenetics, which, integrated with therapeutic drug monitoring, should receive greater consideration, with the aim of personalized therapy.
引用
收藏
页码:941 / 956
页数:16
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