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首页> 外文期刊>The journal of clinical endocrinology and metabolism >Selectively Targeting Mutant BRAF in Thyroid Cancer
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Selectively Targeting Mutant BRAF in Thyroid Cancer

机译:甲状腺癌的选择性靶向突变BRAF

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Whether selective BRAF inhibitors will eventually find a role in thyroid cancer therapy is difficult to predict. An appealing feature of these findings is the striking selectivity for the mutant form of BRAF. Increasingly, a patient’s tumor genotype will come to influence therapeutic de- cision making in advanced thyroid cancer. Lessons learned from the highly selective clinical activity of drugs such as trastuzamab (Herceptin) in patients with Her2/Neu amplified breast cancer, and erlotinib (Tarceva) in epidermal growth factor receptor mutated lung cancer will help to inform clinical trials design in thyroid can- cer. Indeed, it seems quite apparent from this study and recent targeted therapy clinical trials that future trials of BRAF inhibitors in thyroid cancer should be focused on the patient population with BRAF mutations, rather than a broader population including patients with other ras pathway mutations.
机译:选择性BRAF抑制剂是否最终会在甲状腺癌治疗中发挥作用尚难以预测。这些发现的吸引人的特征是对BRAF的突变形式的惊人的选择性。患者的肿瘤基因型将越来越多地影响晚期甲状腺癌的治疗决策。从药物(例如曲妥珠单抗(Herceptin)对Her2 / Neu扩增型乳腺癌患者和埃洛替尼(Tarceva)对表皮生长因子受体突变的肺癌患者)具有高度选择性的临床活性中吸取的经验教训,将有助于为甲状腺癌的临床设计提供依据。 cer。确实,从这项研究和最近的靶向治疗临床试验看来,BRAF抑制剂在甲状腺癌中的未来试验应该更加侧重于BRAF突变的患者人群,而不是更广泛的人群,包括其他ras途径突变的患者。

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