Mittal Kriti, Wood Laura S, Rini Brian I
Cleveland Clinic, Taussig Cancer Institute, 9500 Euclid Avenue Desk R 35, 44195 Cleveland, Ohio USA.
Biol Ther. 2012 Oct 16;2(1):5. doi: 10.1007/s13554-012-0005-2. eCollection 2012.
Targeted agents have revolutionized the management of metastatic renal cell carcinoma (RCC). Axitinib, an inhibitor of vascular endothelial growth factor receptor (VEGFR), has been an important addition to currently available therapies for advanced RCC. Its ability to inhibit VEGFRs at nanomolar concentrations distinguishes it as a potent tyrosine kinase inhibitor, with increased selectivity for VEGFR-1, 2, and 3 at clinically applicable concentrations. The phase 3 AXIS trial has established its superiority in prolonging progression-free survival (PFS) in previously treated RCC patients (median PFS 6.7 months for axitinib vs. 4.7 months for sorafenib). Common toxicities of axitinib include hypertension, diarrhea, nausea, hand-foot syndrome, fatigue, and hypothyroidism. Axitinib-induced diastolic blood pressure elevation may be associated with improved clinical outcome, likely reflecting the "on-target" effect of axitinib. Dose escalation to achieve therapeutic plasma drug levels is of considerable clinical interest. Although axitinib has established efficacy in patients treated with one previous agent, its use in the frontline setting is currently the subject of ongoing research.
靶向药物彻底改变了转移性肾细胞癌(RCC)的治疗方式。阿昔替尼是一种血管内皮生长因子受体(VEGFR)抑制剂,已成为晚期RCC现有治疗方法中的重要补充。它能够在纳摩尔浓度下抑制VEGFR,这使其成为一种强效的酪氨酸激酶抑制剂,在临床适用浓度下对VEGFR-1、2和3具有更高的选择性。3期AXIS试验证实了其在延长既往治疗的RCC患者无进展生存期(PFS)方面的优越性(阿昔替尼组的中位PFS为6.7个月,而索拉非尼组为4.7个月)。阿昔替尼的常见毒性包括高血压、腹泻、恶心、手足综合征、疲劳和甲状腺功能减退。阿昔替尼引起的舒张压升高可能与临床结局改善相关,这可能反映了阿昔替尼的“靶向”效应。增加剂量以达到治疗性血浆药物水平具有相当大的临床意义。尽管阿昔替尼在接受过一种既往治疗药物的患者中已证实有效,但其在一线治疗中的应用目前仍是正在进行的研究课题。