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Regorafenib as a new standard of care in advanced colorectal cancer

机译:RegoraFenib是晚期结直肠癌的新护理标准

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Standard treatment for metastatic colorectal cancer (mCRC) involves chemotherapy based on fluoropyrimidines, oxaliplatin, irinotecan and treatments targeting the angiogenic pathway, and EGFR in RAS wild-type tumors. Regorafenib, an active multikinase inhibitor, demonstrated activity against mCRC in Phase I and II studies. The CORRECT study demonstrated activity of regorafenib in third line versus placebo. The primary end point (overall survival), was met (6.4 vs 5.0 months [hazard ratio: 0.77; 95% Cl: 0.64-0.94; p = 0.0052]). Median progression-free survival was 1.9 versus 1.7 months (hazard ratio: 0.49; 95% Cl: 0.42-0.58; p < 0.0001). Most common adverse events of regorafenib were hand-foot skin reaction, fatigue, diarrhea, hypertension and rash or desquamation and stomatitis, but with a close management and/or dose modifications were controlled. In conclusion, regorafenib is a new standard in third line in mCRC.
机译:转移性结肠直肠癌(MCRC)的标准处理涉及基于氟嘧啶,Oxaliplatin,伊替替康和治疗的化疗,靶向血管生成途径,并在RAS野生型肿瘤中的EGFR。 Regorafenib是一种活性多立糖酶抑制剂,在I和II研究中表明了对MCRC的活性。 正确的研究证明了第三线与安慰剂中的Regorafenib的活性。 达到主要终点(总存活)(6.4 Vs 5.0个月[危险比:0.77; 95%CL:0.64-0.94; p = 0.0052])。 中位的无进展生存率为1.9与1.7个月(危险比:0.49; 95%CL:0.42-0.58; P <0.0001)。 Regorafenib最常见的不良事件是手脚皮肤反应,疲劳,腹泻,高血压和皮疹或脱皮和口腔炎,但是控制了密切的管理和/或剂量修饰。 总之,Regorafenib是MCRC中的第三行的新标准。

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