会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 1. 发明申请
    • METHODS FOR EVALUATING ANGIOGENIC POTENTIAL IN CULTURE
    • 用于评估文化中的生殖潜力的方法
    • US20100216168A1
    • 2010-08-26
    • US12530541
    • 2008-03-24
    • Jamie HeinzmanStacey BrowerJason BushZhibao Mi
    • Jamie HeinzmanStacey BrowerJason BushZhibao Mi
    • G01N33/574
    • G01N33/574G01N33/5011G01N2800/52
    • The present invention provides a method of evaluating the angiogenic potential of a tumor, and for predicting the efficacy of anti-angiogenic therapies on an individualized basis. The method of the invention involves preparing an angiogenic signature for malignant cells in culture by assaying for the presence or level of one or more angiogenesis-related factors selected from VEGF/VPF, IL8/CXCL8, TGF-β1, TGF-β2, TGF-β3, bFGF/FGF-2, EGF, PDGF-AA, PDGF-AA/BB, IP-10, and Flt-3 ligand. The angiogenic signature may be prepared from cultures maintained under normoxic and/or hypoxic environments. The invention may be used in conjunction with chemoresponse testing of anti-tumor agents, to predict or suggest a combination therapy for cancer patients.
    • 本发明提供一种评价肿瘤血管生成潜力的方法,以及用于个体化预测抗血管生成疗法的功效。 本发明的方法包括通过测定选自VEGF / VPF,IL8 / CXCL8,TGF-β1,TGF-β1的一种或多种血管生成相关因子的存在或水平来制备培养中恶性细胞的血管生成特征。 2,TGF-βb,3,bFGF / FGF-2,EGF,PDGF-AA,PDGF-AA / BB,IP-10和Flt-3配体。 血管生成特征可以由维持在常氧和/或缺氧环境下的培养物制备。 本发明可以与抗肿瘤剂的化学应答测试结合使用,以预测或建议癌症患者的联合疗法。
    • 5. 发明申请
    • METHODS FOR PREDICTING A PATIENT'S RESPONSE TO EGFR INHIBITORS
    • 方法预防患者对EGFR抑制剂的反应
    • US20100311084A1
    • 2010-12-09
    • US12795286
    • 2010-06-07
    • Stacey BrowerShara D. RiceTheresa R. CassinoLahari SakhamuriHeather M. BuechelLauren M. Hancher
    • Stacey BrowerShara D. RiceTheresa R. CassinoLahari SakhamuriHeather M. BuechelLauren M. Hancher
    • G01N33/574
    • G01N33/5091G01N33/574G01N2333/485G01N2800/52
    • The present invention provides methods for individualizing chemotherapy for cancer treatment, and particularly for evaluating a patient's responsiveness to one or more epidermal growth factor receptor (EGFR) inhibitors prior to treatment with such agents. Particularly, the invention provides an in vitro chemoresponse assay for predicting a patient's response to a monoclonal EGFR antibody, such as cetuximab. The method generally comprises culturing malignant cells from a patient's specimen (e.g., biopsy specimen), contacting the cultured cells with a monoclonal EGFR antibody that is a candidate treatment for the patient, and evaluating the cultured cells for a response to the drug. In certain embodiments, monolayer(s) of malignant cells are cultured from explants prepared by mincing tumor tissue, and the cells of the monolayer are suspended and plated for chemosenstivity testing. The in vitro response to the drug as determined by the method of the invention is correlative with the patient's in vivo response upon receiving the monoclonal EGFR antibody during chemotherapeutic treatment (e.g., in combination with other standardized or individualized chemotherapeutic regimen).
    • 本发明提供了用于个体化癌症治疗化学疗法的方法,特别是用于评估患者在用这些药物治疗之前对一种或多种表皮生长因子受体(EGFR)抑制剂的反应性。 特别地,本发明提供了用于预测患者对单克隆EGFR抗体如西妥昔单抗的应答的体外化学应答测定。 该方法通常包括从患者标本(例如活检标本)培养恶性细胞,使培养的细胞与作为患者候选治疗的单克隆EGFR抗体接触,并评价培养细胞对药物的应答。 在某些实施方案中,从通过切割肿瘤组织制备的外植体培养恶性细胞的单层,并将单层细胞悬浮并铺板以进行化学敏感性测试。 通过本发明的方法确定的对药物的体外应答与在化疗期间接受单克隆EGFR抗体(例如,与其他标准化或个体化化学治疗方案组合)时患者体内应答相关。