首页|免疫检查点抑制剂联合安罗替尼治疗晚期非小细胞肺癌的临床疗效

免疫检查点抑制剂联合安罗替尼治疗晚期非小细胞肺癌的临床疗效

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目的 探讨免疫检查点抑制剂(ICIs)与安罗替尼联合治疗晚期非小细胞肺癌(NSCLC)患者的效果和耐受性。方法 选取2019年12月至2023年12月安徽省第二人民医院收治的三线及以上晚期NSCLC患者,根据治疗方案分为安罗替尼治疗的单药组和ICIs联合安罗替尼治疗的联合组。依据实体瘤疗效评价标准比较两组患者的治疗效果和不良反应。结果 共纳入45例患者,单药组25例,联合组20例。随访截至2024年2月,中位随访时间为11。9(3。0~26。0)个月。单药组和联合组患者的客观缓解率(ORR)分别为12。0%和15。0%,疾病控制率(DCR)分别为80。0%和90。0%,两组比较差异均无统计学意义(P>0。05)。与单药组相比,联合组患者有更长的中位无进展生存期(PFS,6。40个月比3。00个月)和中位总生存期(OS,10。20个月比6。30个月),差异有统计学意义(P<0。05)。多发转移和三线以上治疗线数是NSCLC患者PFS和OS的独立危险因素,ICIs联合安罗替尼治疗则为独立保护因素。两组患者治疗后的血清癌胚抗原、细胞角蛋白19片段和鳞状细胞癌抗原均低于本组治疗前,且联合组上述指标均低于单药组,差异均有统计学意义(P<0。05)。两组均无严重不良反应发生。结论 ICIs与安罗替尼联合治疗晚期NSCLC可延长患者生存期,且安全性可控。
Clinical efficacy of immune checkpoint inhibitors combined with anlotinib in the treatment of advanced non-small cell lung cancer
Objective To investigate the efficacy and tolerability of immune checkpoint inhibitors(ICIs)combined with anlotinib as a subsequent-line treatment for patients with advanced non-small cell lung cancer(NSCLC).Methods Patients with advanced NSCLC who received three or more lines of treatment and were admitted to Anhui No.2 Provincial People's Hospital from December 2019 to December 2023 were selected and divided into a monotherapy group treated with anlotinib alone and a combination group treated with ICIs in combination with anlotinib,based on their treatment regimens.The therapeutic effects and adverse reactions between the two groups were compared using the response evaluation criteria in solid tumors.Results A total of 45 patients were included,with 25 cases in the monotherapy group and 20 cases in the combination group.With a median follow-up time of 11.9(3.0 to 26.0)months as of February 2024,the objective response rates(ORR)were 12.0%and 15.0%,and the disease control rates(DCR)were 80.0%and 90.0%in monotherapy group and combination group,respectively,and these differences were not statistically significant(P>0.05).Compared to the monotherapy group,patients in the combination group had longer median progression-free survival(PFS,6.40 months vs 3.00 months)and median overall survival(OS,10.20 months vs 6.30 months),with statistical significance(P<0.05).Multiple metastases and more than three lines of treatment were identified as independent risk factors for both PFS and OS in NSCLC patients,while the combination therapy of ICIs with anlotinib served as an independent protective factor.Serum levels of carcinoembryonic antigen,cytokeratin 19 fragment,and squamous cell carcinoma antigen levels were all reduced post-treatment compared to pre-treatment in both groups,with lower levels observed in the combination group compared to the monotherapy group(P<0.05).No severe adverse reactions occurred in both group.Conclusion The combination of ICIs with anlotinib as a subsequent-line treatment for advanced NSCLC can prolong patient survival with manageable safety.

immune checkpoint inhibitorsanlotinibadvanced non-small cell lung cancerclinical efficacy

洪乔军、韩冬冬、方瑜、王章桂、周道平

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安徽省第二人民医院 肿瘤科,合肥 230032

免疫检查点抑制剂 安罗替尼 晚期非小细胞肺癌 临床疗效

2024

临床药物治疗杂志
北京药学会

临床药物治疗杂志

CSTPCD
影响因子:1.07
ISSN:1672-3384
年,卷(期):2024.22(8)