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余旭旭, 李向柯, 杨闽洁, 陈钟, 毛迎港, 宋丽杰. PD-1抑制剂联合安罗替尼治疗晚期神经内分泌癌的疗效及安全性[J]. 肿瘤防治研究, 2021, 48(10): 974-978. DOI: 10.3971/j.issn.1000-8578.2021.21.0271
引用本文: 余旭旭, 李向柯, 杨闽洁, 陈钟, 毛迎港, 宋丽杰. PD-1抑制剂联合安罗替尼治疗晚期神经内分泌癌的疗效及安全性[J]. 肿瘤防治研究, 2021, 48(10): 974-978. DOI: 10.3971/j.issn.1000-8578.2021.21.0271
YU Xuxu, LI Xiangke, YANG Minjie, CHEN Zhong, MAO Yinggang, SONG Lijie. Efficacy and Safety of PD-1 Inhibitor Combined with Anlotinib on Advanced Neuroendocrine Carcinoma[J]. Cancer Research on Prevention and Treatment, 2021, 48(10): 974-978. DOI: 10.3971/j.issn.1000-8578.2021.21.0271
Citation: YU Xuxu, LI Xiangke, YANG Minjie, CHEN Zhong, MAO Yinggang, SONG Lijie. Efficacy and Safety of PD-1 Inhibitor Combined with Anlotinib on Advanced Neuroendocrine Carcinoma[J]. Cancer Research on Prevention and Treatment, 2021, 48(10): 974-978. DOI: 10.3971/j.issn.1000-8578.2021.21.0271

PD-1抑制剂联合安罗替尼治疗晚期神经内分泌癌的疗效及安全性

Efficacy and Safety of PD-1 Inhibitor Combined with Anlotinib on Advanced Neuroendocrine Carcinoma

  • 摘要:
    目的 分析程序性死亡受体-1(PD-1)抑制剂联合安罗替尼治疗晚期神经内分泌癌的疗效及安全性。
    方法 收集郑州大学第一附属医院经一线标准化疗失败、应用PD-1抑制剂联合安罗替尼治疗的晚期神经内分泌癌患者资料。
    结果 共纳入45例患者,男性24例,女性21例;年龄42~84岁,中位年龄57岁。肿瘤原发部位:肺23例(51.1%)、食管8例(17.8%)、胰腺和直肠各7例(15.6%)。18例(40.0%)患者既往一线和二线治疗失败,27例(60.0%)患者三线及以上治疗失败。所有患者接受2~15周期的治疗,3例因疾病进展死亡,总体客观缓解率为11.1%,疾病控制率为53.5%,中位无进展生存期为5.8月,10月无进展生存率为25.5%。不良反应主要为1~2级骨髓抑制和消化道反应。
    结论 PD-1联合安罗替尼治疗晚期神经内分泌癌疗效较好,耐受性好,可作为晚期神经内分泌癌标准一线治疗失败后的选择。

     

    Abstract:
    Objective To analyze the efficacy and safety of PD-1 inhibitor combined with anlotinib on advanced neuroendocrine carcinoma.
    Methods We collected the data of patients with advanced neuroendocrine carcinoma who had failed the first-line standard chemotherapy and treated with PD-1 inhibitor combined with anlotinib from the First Affiliated Hospital of Zhengzhou University.
    Results A total of 45 patients, including 24 males and 21 females, were included. The median age was 57 years old. The primary tumor sites were lung (23 cases, 51.1%), esophagus (8 cases, 17.8%), pancreas (7 cases, 15.6%) and rectum (7 cases, 15.6%). Eighteen cases (40%) had failed the first- and second-line treatments, and 27 cases (60%) had failed the third-line and above treatments. All patients received 2-15 cycles of treatment, 3 cases died due to disease progression, overall objective response rate was 11.1%, disease control rate was 53.5%, median progression-free survival was 5.8 months, and 10-month progression-free survival rate was 25.5%. Adverse events were mainly grade 1-2 myelosuppression and digestive tract reactions.
    Conclusion PD-1 combined with anlotinib show better efficacy and good tolerance on advanced neuroendocrine carcinoma. It can be used as a choice after the failure of standard first-line treatment of advanced neuroendocrine carcinoma.

     

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