阿昔替尼联合信迪利单抗治疗中高危晚期肾癌的研究

杜羽 斯璐 毛丽丽 迟志宏 崔传亮 郭军

杜羽, 斯璐, 毛丽丽, 迟志宏, 崔传亮, 郭军. 阿昔替尼联合信迪利单抗治疗中高危晚期肾癌的研究[J]. 中国肿瘤临床, 2020, 47(10): 513-516. doi: 10.3969/j.issn.1000-8179.2020.10.342
引用本文: 杜羽, 斯璐, 毛丽丽, 迟志宏, 崔传亮, 郭军. 阿昔替尼联合信迪利单抗治疗中高危晚期肾癌的研究[J]. 中国肿瘤临床, 2020, 47(10): 513-516. doi: 10.3969/j.issn.1000-8179.2020.10.342
Du Yu, Si Lu, Mao Lili, Chi Zhihong, Cui Chuanliang, Guo Jun. Efficacy of axitinib plus sintilimab in intermediate-and high-risk advanced renal cell carcinoma[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2020, 47(10): 513-516. doi: 10.3969/j.issn.1000-8179.2020.10.342
Citation: Du Yu, Si Lu, Mao Lili, Chi Zhihong, Cui Chuanliang, Guo Jun. Efficacy of axitinib plus sintilimab in intermediate-and high-risk advanced renal cell carcinoma[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2020, 47(10): 513-516. doi: 10.3969/j.issn.1000-8179.2020.10.342

阿昔替尼联合信迪利单抗治疗中高危晚期肾癌的研究

doi: 10.3969/j.issn.1000-8179.2020.10.342
详细信息
    作者简介:

    杜羽  专业方向为肾癌的分子靶向及免疫治疗。E-mail:dyuu0225@163.com

    通讯作者:

    郭军  guoj307@126.com

Efficacy of axitinib plus sintilimab in intermediate-and high-risk advanced renal cell carcinoma

More Information
  • 摘要:   目的  评价阿昔替尼联合信迪利单抗治疗中高危晚期肾癌的初步疗效及安全性。  方法  回顾性分析2019年4月至2019年12月10例就诊于北京大学肿瘤医院行阿昔替尼联合信迪利单抗治疗的晚期肾癌患者的临床资料,其中病理诊断为肾透明细胞癌患者7例、肾非透明细胞癌3例。治疗方案为静脉滴注信迪利单抗200 mg、每3周1次,口服阿昔替尼5 mg、每天2次,并分析客观缓解率、无进展生存期及不良反应。  结果  所有患者中位年龄为58.5(43.0~67.0)岁,国际转移性肾细胞癌数据库联盟(interna?tional metastatic renal cell carcinoma database consortium,IMDC)风险分级均为中危或高危。10例患者的阿昔替尼联合信迪利单抗的客观缓解率为40.0%(4/10),疾病控制率为90.0%(9/10)。7例肾透明细胞癌患者的客观缓解率为57.1%(4/7)。10例患者的主要不良反应中转氨酶升高4例(40.0%),甲状腺功能减退症4例(40.0%),恶心3例(30.0%),高血压2例(20.0%),手足皮肤反应2例(20.0%)。患者的不良反应主要为1~2级,3例发生3~4级不良反应,经对症治疗好转。  结论  阿昔替尼联合信迪利单抗治疗中高危晚期肾癌有较高的客观缓解率,且不良反应多可耐受。

     

  • 图  1  10例肾癌患者的治疗反应及持续时间

    图  2  1例肾透明细胞癌患者肺转移假性进展的胸部CT

    A:基线;B:治疗8周;C:治疗16周

    表  1  10例肾癌患者一般特征

    表  2  10例肾癌患者行阿昔替尼联合信迪利单抗的不良反应

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出版历程
  • 收稿日期:  2020-03-30
  • 刊出日期:  2020-12-26

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