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首页> 外文期刊>Obstetrical and gynecological survey >Anti-Angiopoietin Therapy With Trebananib for Recurrent Ovarian Cancer (TRINOVA-1): A Randomised, Multicentre, Double-blind, Placebo-Controlled Phase 3 Trial
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Anti-Angiopoietin Therapy With Trebananib for Recurrent Ovarian Cancer (TRINOVA-1): A Randomised, Multicentre, Double-blind, Placebo-Controlled Phase 3 Trial

机译:Trebananib抗血管生成素疗法治疗复发性卵巢癌(TRINOVA-1):一项随机,多中心,双盲,安慰剂对照的3期试验

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摘要

Angiogenesis has become an important target for treatment of epithelial ovarian cancer. The growth of new blood vessels iscritical for cancer growth, metastases, and progression. Vascular endothelial growth factor (VEGF) plays a key role in epithelial ovarian cancer. Adding anti-VEGF treatment to first-line chemotherapy, to maintenance therapy, or at the time of recurrence significantly prolongs progression-free survival. However, these agents have several adverse effects, including hypertension, thrombosis, emboli, bleeding, impaired wound healing, proteinuria, and bowel perforation. As many as a third of patients with epithelial ovarian cancer discontinue anti-VEGF treatment because of these adverse events.Trebananib has a mechanism of action and toxicity profile different from other antiangiogenesis agents. It inhibits angiogenesis by preventing the binding of angiopoietins 1 and 2 to the Tie2 receptor. In a randomized phase 2 trial, trebananib prolonged progression-free survival in patients with recurrent epithelial ovarian cancer. This agent has mild and reversible adverse events. Edema is a unique adverse effect.
机译:血管生成已成为治疗上皮性卵巢癌的重要靶标。新血管的生长对于癌症的生长,转移和进展至关重要。血管内皮生长因子(VEGF)在上皮性卵巢癌中起关键作用。在第一线化疗,维持治疗或复发时添加抗VEGF治疗可显着延长无进展生存期。但是,这些药物有几种不良反应,包括高血压,血栓形成,栓子,出血,伤口愈合不良,蛋白尿和肠穿孔。由于这些不良事件,多达三分之一的上皮性卵巢癌患者中止了抗VEGF治疗。曲巴尼单抗的作用机理和毒性谱与其他抗血管生成剂不同。它通过阻止血管生成素1和2与Tie2受体的结合来抑制血管生成。在一项随机的2期临床试验中,trebananib延长了复发性上皮性卵巢癌患者的无进展生存期。该药物有轻度和可逆的不良事件。水肿是一种独特的不良反应。

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