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卡瑞利珠单抗联合安罗替尼三线治疗晚期非小细胞肺癌的疗效观察

张晓娟, 岳冬丽, 杨双宁, 郝娜, 王丽萍, 董文杰

张晓娟, 岳冬丽, 杨双宁, 郝娜, 王丽萍, 董文杰. 卡瑞利珠单抗联合安罗替尼三线治疗晚期非小细胞肺癌的疗效观察[J]. 肿瘤防治研究, 2023, 50(6): 593-597. DOI: 10.3971/j.issn.1000-8578.2023.22.0098
引用本文: 张晓娟, 岳冬丽, 杨双宁, 郝娜, 王丽萍, 董文杰. 卡瑞利珠单抗联合安罗替尼三线治疗晚期非小细胞肺癌的疗效观察[J]. 肿瘤防治研究, 2023, 50(6): 593-597. DOI: 10.3971/j.issn.1000-8578.2023.22.0098
ZHANG Xiaojuan, YUE Dongli, YANG Shuangning, HAO Na, WANG Liping, DONG Wenjie. Efficacy of Combination of Camrelizumab with Anlotinib as Third-line Therapy for Patients with Advanced Non-small Cell Lung Cancer[J]. Cancer Research on Prevention and Treatment, 2023, 50(6): 593-597. DOI: 10.3971/j.issn.1000-8578.2023.22.0098
Citation: ZHANG Xiaojuan, YUE Dongli, YANG Shuangning, HAO Na, WANG Liping, DONG Wenjie. Efficacy of Combination of Camrelizumab with Anlotinib as Third-line Therapy for Patients with Advanced Non-small Cell Lung Cancer[J]. Cancer Research on Prevention and Treatment, 2023, 50(6): 593-597. DOI: 10.3971/j.issn.1000-8578.2023.22.0098

卡瑞利珠单抗联合安罗替尼三线治疗晚期非小细胞肺癌的疗效观察

基金项目: 

国家自然科学基金面上项目 81872410

详细信息
    作者简介:

    张晓娟(1996-),女,硕士在读,主要从事肺癌的早期诊断和综合治疗,ORCID: 0009-0005-3640-1249

    通信作者:

    王丽萍(1963-),女,博士,主任医师,主要从事肺癌的早期诊断和综合治疗,E-mail: wlp@zzu.edu.cn

    董文杰(1981-),男,博士,副主任医师,主要从事肺癌及消化道肿瘤的诊断和综合治疗,E-mail: dongwenjie200581@126.com

  • 中图分类号: R734.2

Efficacy of Combination of Camrelizumab with Anlotinib as Third-line Therapy for Patients with Advanced Non-small Cell Lung Cancer

Funding: 

National Natural Science Foundation of China 81872410

More Information
  • 摘要:
    目的 

    探讨卡瑞利珠单抗联合安罗替尼三线治疗晚期非小细胞肺癌的临床疗效及安全性。

    方法 

    回顾性分析84例二线治疗进展后的晚期非小细胞肺癌患者的临床资料。其中44例接受卡瑞利珠单抗联合安罗替尼治疗的患者为观察组,40例接受单药安罗替尼治疗的患者为对照组。比较两组无进展生存期(PFS)、客观缓解率(ORR)、疾病控制率(DCR)和不良事件(AE)发生率。

    结果 

    观察组的中位PFS长于对照组(7.0月vs. 5.6月, P=0.001)。两组ORR及DCR差异无统计学意义(P=0.112, P=0.508)。两组AE及≥3级AE发生率差异均无统计学意义(P=0.222, P=0.112)。

    结论 

    卡瑞利珠单抗联合安罗替尼三线治疗晚期非小细胞肺癌的临床疗效优于单用安罗替尼,且安全性良好。

     

    Abstract:
    Objective 

    To investigate the clinical efficacy and related adverse reactions of the combination of camrelizumab with anlotinib as the third-line therapy on advanced non-small cell lung cancer.

    Methods 

    We retrospectively analyzed the clinical data of 84 patients with advanced non-small cell lung cancer after second-line treatment. According to different treatment methods, 44 patients who received camrelizumab combined with anlotinib were included in the observation group, and 40 patients who received anlotinib alone were included in the control group. The PFS, ORR, DCR and incidence of adverse reactions were analyzed and compared between the two groups.

    Results 

    The median PFS of the observation group was longer than that of the control group (7.0 vs. 5.6 months, P=0.001). No statistically significant difference was observed in ORR, DCR, the incidence of adverse reactions or the incidence of adverse reactions above grade 3 between two groups (all P > 0.05).

    Conclusion 

    The clinical efficacy of camrelizumab combined with anlotinib as third-line therapy on advanced non-small cell lung cancer is better than anlotinib alone, and the safety is good.

     

  • Competing interests: The authors declare that they have no competing interests.
    利益冲突声明:
    所有作者均声明不存在利益冲突。
    作者贡献:
    张晓娟:选题设计、资料与数据收集、文章撰写和修改
    岳冬丽:选题设计、数据收集
    杨双宁、郝娜:数据收集
    王丽萍、董文杰:指导选题与设计、指导文章写作与修改
  • 图  1   卡瑞利珠单抗联合安罗替尼组与单药安罗替尼组PFS的比较

    Figure  1   Comparison of PFS between observation group and control group

    表  1   卡瑞利珠单抗联合安罗替尼组与单药安罗替尼组一般临床资料(n(%))

    Table  1   General clinical data of camrelizumab combined with anlotinib (observation) group and anlotinib alone (control) group (n(%))

    下载: 导出CSV

    表  2   卡瑞利珠单抗联合安罗替尼组与单药安罗替尼组患者短期疗效比较(n(%))

    Table  2   Comparison of short-term efficacy between observation group and control group (n(%))

    下载: 导出CSV

    表  3   卡瑞利珠单抗联合安罗替尼组与单药安罗替尼组不良反应发生率比较(n(%))

    Table  3   Comparison of the incidence of adverse effects between observation group and group group (n(%))

    下载: 导出CSV

    表  4   卡瑞利珠单抗联合安罗替尼组与单药安罗替尼组≥3级不良反应发生率比较(n(%))

    Table  4   Comparison of the incidence of grade ≥3 adverse reactions between observation group and control group (n(%))

    下载: 导出CSV
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出版历程
  • 收稿日期:  2022-01-27
  • 修回日期:  2022-04-27
  • 网络出版日期:  2024-01-12
  • 刊出日期:  2023-06-24

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