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Clinical study of apatinib combined with EGFR‐TKI in the treatment of chronic progression after EGFR‐TKI treatment in non‐small cell lung cancer (ChiCTR1800019185)

机译:临床研究与EGFR-TKI结合EGFR-TKI治疗非小细胞肺癌EGFR-TKI治疗后慢性进展(CHICTR1800019185)

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This clinical trial (ChiCTR1800019185) is designed to be an open-label, prospective, single-center, single arm exploratory research study. The study will recruit non-small cell lung cancer patients (NSCLC) with slow progression after first-line treatment with EGFR-TKI drugs. Slow progression will be confirmed by the presence of serum carcinoembryonic antigen or imaging evaluation. The primary aim is to assess progression-free survival after EGFR-TKIs treatment combined with apatinib 250?mg once daily. The secondary objectives are to evaluate objective efficacy, disease control rates, quality of life, overall survival, and safety. From September 2018 to September 2020, under specific entry and discharge standards, we plan to enroll 38 eligible patients until the end of the study. We hope that our study will help to explore a new way of combining the small molecular inhibitors of antiangiogenesis with EGFR-TKIs to overcome acquired drug resistance.? 2020 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd.
机译:该临床试验(CHICTR1800019185)旨在成为开放式,前瞻性,单中心的单一手臂探索研究。该研究将募集非小细胞肺癌患者(NSCLC),在用EGFR-TKI药物的一线治疗后进展缓慢。通过存在血清癌胚抗原或影像学评估,将确认缓慢的进展。主要目的是评估EGFR-TKIS治疗后的无进展生存期,并每天一次加入Apatinib 250毫克。次要目标是评估客观疗效,疾病控制率,生活质量,整体生存和安全。从2018年9月到2020年9月,根据具体的入学和排放标准,我们计划在研究结束之前注册38名符合条件的患者。我们希望我们的研究将有助于探索与EGFR-TKIS结合抗脑发生的小分子抑制剂以克服获得的耐药性的新方法。 2020作者。中国肺部肿瘤集团和约翰瓦里和儿子澳大利亚发表的胸癌

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