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首页> 外文期刊>Cancer discovery. >Efficacy of BGJ398, a Fibroblast Growth Factor Receptor 1-3 Inhibitor, in Patients with Previously Treated Advanced Urothelial Carcinoma with FGFR3 Alterations
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Efficacy of BGJ398, a Fibroblast Growth Factor Receptor 1-3 Inhibitor, in Patients with Previously Treated Advanced Urothelial Carcinoma with FGFR3 Alterations

机译:BGJ398,成纤维细胞生长因子受体1-3抑制剂的功效,以先前治疗的先进尿路上皮癌,FGFR3改变

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摘要

BGJ398, a potent and selective pan-FGFR antagonist, was prospectively evaluated in patients with metastatic urothelial carcinoma bearing a diverse array of FGFR3 alterations. Patients (N = 67) who were unable to receive platinum chemotherapy were enrolled. The majority (70.1%) had received two or more prior antineoplastic therapies. BGJ398 was administered orally at 125 mg/day on a 3 weeks on, 1 week off schedule until unacceptable toxicity or progression. The primary endpoint was the response rate. Among 87 patients treated, an overall response rate of 25.4% was observed and an additional 38.8% of patients had disease stabilization, translating to a disease control rate of 64.2%. The most common treatment-emergent toxicities were hyperphosphatemia, elevated creatinine, fatigue, constipation, and decreased appetite. Further examination of BGJ398 in this disease setting is warranted.
机译:BGJ398,一种有效和选择性的Pan-FGFR拮抗剂,在转移性尿路上皮癌患者中进行了预期评估,其中轴承是一种不同的FGFR3改变。 注册了无法接受铂化疗的患者(n = 67)。 大多数(70.1%)接受了两种或更多种以上的抗肿瘤疗法。 BGJ398在3周内在125毫克/天口服施用,每次截止时间表,直至不可接受的毒性或进展。 主要终点是响应率。 在治疗的87名患者中,观察到25.4%的总反应率,另外38.8%的患者患有疾病稳定性,转化为疾病控制率为64.2%。 最常见的治疗紧急毒性是高磷血症,肌酐升高,疲劳,便秘和食欲下降。 进一步检查该疾病环境中的BGJ398。

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