首页|安罗替尼联合免疫检查点抑制剂治疗晚期肺癌的效果分析

安罗替尼联合免疫检查点抑制剂治疗晚期肺癌的效果分析

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目的 探索安罗替尼联合免疫检查点抑制剂治疗晚期肺癌的疗效及安全性.方法 回顾性分析118例肺癌患者的临床资料,根据治疗方法不同将所有患者分为单药组(56例)和联合组(62例).单药组采用安罗替尼口服治疗,联合组采用安罗替尼联合免疫检查点抑制剂治疗.比较两组患者近期疗效;无进展生存时间(PFS);查尔森合并症指数 0~1 分、治疗线数≤2 线患者的PFS;不良反应发生情况.结果 单药组无完全缓解(CR)患者,部分缓解(PR)4 例(7.1%),疾病稳定(SD)41 例(73.2%),疾病进展(PD)11 例(19.6%);联合组无CR患者,PR 17 例(27.4%),SD 37 例(59.7%),PD 8 例(12.9%).联合组的客观缓解率(ORR)27.4%高于单药组的 7.1%,差异有统计学意义(P<0.05);疾病控制率(DCR)87.1%略高于单药组的 80.4%,差异无统计学意义(P>0.05).联合组中位PFS为 4.1 个月,长于单药组的 3.0 个月(P<0.05).联合组查尔森合并症指数 0~1 分患者、治疗线数≤2 线中位PFS分别为 5.0、7.0 个月,均长于单药组的 3.8、4.4 个月,差异有统计学意义(P<0.05).单药组高血压发生率为 19.6%(11/56),乏力发生率为 14.3%(8/56),尿蛋白发生率为 7.1%(4/56),内分泌异常发生率为 5.3%(3/56).联合组高血压发生率为 16.1%(10/62),乏力发生率为 16.1%(10/62),内分泌异常发生率为 11.3%(7/62),肝功能异常发生率为9.7%(6/62),免疫性肺炎发生率为 4.8%(3/62).单药组 3 级高血压患者为 2 例,联合组 3 级高血压患者为3 例,其余均为 1~2 级高血压.停药并治疗均好转.结论 安罗替尼联合免疫检查点抑制剂治疗晚期肺癌具有安全性.但治疗越进入晚期治疗效果越差;查尔森合并症指数 0~1 分、治疗线数≤2 线的患者采用联合用药治疗在延长PFS方面可能更有优势.
Effect analysis of anlotinib combined with immune checkpoint inhibitors in the treatment of advanced lung cancer
Objective To investigate the efficacy and safety of anlotinib combined with immune checkpoint inhibitors for patients with advanced lung cancer.Methods Clinical data of 118 patients with lung cancer were retrospectively analyzed.According to different treatment methods,all patients were divided into single-agent group(56 cases)and combined group(62 cases).The single-agent group was treated with oral antirotinib,and the combined group was treated with antirotinib combined with immune checkpoint inhibitors.The short-term efficacy,progression free survival(PFS),PFS of patients with Charlson comorbidity index of 0-1 points and patients in first or second-line treatment,and occurrence of adverse reactions were compared between the two groups.Results In the single-agent group,there were no complete response(CR),partial response(PR)in 4 cases(7.1%),stable disease(SD)in 41 cases(73.2%),and progressive disease(PD)in 11 cases(19.6%).In the combined group,there were 17 cases(27.4%)of CR,37 cases(59.7%)of SD and 8 cases(12.9%)of PD.The objective response rate(ORR)of 27.4%in the combined group was higher than 7.1%in the single-agent group,and the difference was statistically significant(P<0.05);the disease control rate(DCR)of 87.1%was slightly higher than 80.4%in the single-agent group,but the difference was not statistically significant(P>0.05).The median PFS in the combined group was 4.1 months,which was longer than 3.0 months in the single-agent group(P<0.05).The median PFS of patients with Charlson comorbidity index of 0-1 points and patients in first or second-line treatment in combined group were 5.0 and 7.0 months,which were longer than 3.8 and 4.4 months in single-agent group,and the difference was statistically significant(P<0.05).In the single-agent group,the incidence of hypertension was 19.6%(11/56),the incidence of fatigue was 14.3%(8/56),the incidence of urinary protein was 7.1%(4/56)and the incidence of endocrine abnormality was 5.3%(3/56).In the combined group,the incidence of hypertension was 16.1%(10/62),the incidence of fatigue was 16.1%(10/62),the incidence of endocrine abnormality was 11.3%(7/62),the incidence of liver function abnormality was 9.7%(6/62)and the incidence of immune pneumonia was 4.8%(3/62).There were 2 patients with grade 3 hypertension in the single-agent group,3 patients with grade 3 hypertension in the combined group,and the rest were grade 1-2 hypertension.All patients were improved after withdrawal of medication and treatment.Conclusion Allotinib combined with immune checkpoint inhibitors is safe in the treatment of advanced lung cancer.However,the more advanced the treatment,the worse the therapeutic effect.Combination therapy has an advantage in prolonging PFS for patients with Charlson comorbidity index of 0-1 points and patients in first or second-line treatment.

Advanced lung cancerAnlotinibImmune checkpoint inhibitors

张琼妍、周颐、朱娴雅、曾丽丽、王静、孙杨承

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215128 苏州市吴中人民医院肿瘤内科

晚期肺癌 安罗替尼 免疫检查点抑制剂

2024

中国实用医药
中国康复医学会

中国实用医药

影响因子:0.797
ISSN:1673-7555
年,卷(期):2024.19(4)
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