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Identification of mutation in LKB1 as a predictive biomarker for sensitivity to TOR kinase inhibitors

机译:鉴定LKB1中的突变作为对TOR激酶抑制剂敏感性的预测生物标志物

摘要

A TOR kinase inhibitor for use in a method of treating non-small cell carcinoma of the lung, cervical cancer, or Peutz-Jeghers syndrome, in which the method comprises administering the TOR kinase inhibitor to a patient who has non-small cell lung carcinoma, cancer of the cervix or Peutz-Jeghers syndrome characterized by a loss of or mutation in the LKB1 gene or protein, compared to the wild type, in which the TOR kinase inhibitor is 7- ( 6- (2-hydroxypropan-2-yl) pyridin-3-yl) -1- (trans-4-methoxycyclohexyl) - 3,4-dihydropyrazino [2,3-b] pyrazin-2 (1H) -one or a salt, clathrate, solvate, stereoisomer or tautomer of this pharmaceutically acceptable.
机译:在治疗非小细胞肺癌,子宫颈癌或Peutz-Jeghers综合征的方法中使用的TOR激酶抑制剂,其中该方法包括向患有非小细胞肺癌的患者施用TOR激酶抑制剂子宫颈癌或Peutz-Jeghers综合征的癌症,特征在于与野生型相比,LKB1基因或蛋白质缺失或突变,而TOR激酶抑制剂为7-(6-(2-羟丙-2-基)吡啶-3-基)-1-(反式-4-甲氧基环己基)-3,4-二氢吡嗪并[2,3-b]吡嗪2(1H)-一种或多种的盐,包合物,溶剂化物,立体异构体或互变异构体这种药学上可接受的。

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