METHODS OF TREATING CANCER
    67.
    发明申请
    METHODS OF TREATING CANCER 审中-公开
    癌症治疗方法

    公开(公告)号:US20160067307A1

    公开(公告)日:2016-03-10

    申请号:US14785691

    申请日:2014-04-30

    IPC分类号: A61K38/17

    CPC分类号: A61K38/179

    摘要: Methods of treating cancers comprising FGFR1 gene amplification, FGFR1 overexpression, FGFR3 overexpression, FGFR3 amplification, FGF2 overexpression, and/or FGF2 gene amplification are provided. In some embodiments, the methods comprise administering a fibroblast growth factor receptor 1 (FGFR1) extracellular domain (ECD) and/or an FGFR1 ECD fusion molecule. In some embodiments, the methods comprise administering a FGFR1 ECD and/or an FGFR1 ECD fusion molecule in combination with at least one additional therapeutic agent. In some embodiments, methods of treating cancers comprising administering a FGFR1 ECD and/or an FGFR1 ECD fusion molecule in combination with at least one chemotherapeutic agent are provided.

    摘要翻译: 提供了治疗包括FGFR1基因扩增,FGFR1过表达,FGFR3过表达,FGFR3扩增,FGF2过表达和/或FGF2基因扩增的癌症的方法。 在一些实施方案中,所述方法包括施用成纤维细胞生长因子受体1(FGFR1)细胞外结构域(ECD)和/或FGFR1 ECD融合分子。 在一些实施方案中,所述方法包括与至少一种另外的治疗剂组合施用FGFR1 ECD和/或FGFR1 ECD融合分子。 在一些实施方案中,提供了治疗癌症的方法,包括与至少一种化学治疗剂组合施用FGFR1 ECD和/或FGFR1 ECD融合分子。

    Treatment of cancer with elevated dosages of soluble FGFR1 fusion proteins
    70.
    发明授权
    Treatment of cancer with elevated dosages of soluble FGFR1 fusion proteins 有权
    用可溶性FGFR1融合蛋白提高剂量治疗癌症

    公开(公告)号:US08920800B2

    公开(公告)日:2014-12-30

    申请号:US13913292

    申请日:2013-06-07

    发明人: Harold Keer

    摘要: The present invention provides methods of treating a patient having a cancer comprising administering to the patient a soluble Fibroblast Growth Factor Receptor 1 (FGFR1) fusion protein such as an extracellular domain of an FGFR1 polypeptide linked to an Fc polypeptide or another fusion partner. The fusion protein may be administered at a dose of at least about 2 mg/kg body weight. In some embodiments, the patient has a fibroblast growth factor-2 (FGF-2) plasma concentration of at least 6 pg/ml. In some embodiments, the cancer is characterized by a Fibroblast Growth Factor Receptor 2 (FGFR2) having a ligand-dependent activating mutation.

    摘要翻译: 本发明提供了治疗患有癌症的患者的方法,包括向患者施用可溶性成纤维细胞生长因子受体1(FGFR1)融合蛋白,例如与Fc多肽或另一融合配偶体连接的FGFR1多肽的细胞外结构域。 融合蛋白可以以至少约2mg / kg体重的剂量施用。 在一些实施方案中,患者具有至少6pg / ml的成纤维细胞生长因子-2(FGF-2)血浆浓度。 在一些实施方案中,癌症的特征在于具有配体依赖性激活突变的成纤维细胞生长因子受体2(FGFR2)。