摘要
目的观察阿法替尼在晚期肺鳞癌患者二线治疗中的疗效及不良反应,探讨其临床应用价值。方法收集蚌埠医科大学第一附属医院2020年3月—2022年10月驱动基因阴性的晚期肺鳞癌患者58例,按指南予以阿法替尼40 mg/d,口服,发生3级以上副反应时,停药至患者恢复,重新用药剂量按10 mg/次下调,最低至20 mg/d。按实体瘤疗效评价标准1.1版每6周评价1次,至疾病进展,观察疗效及不良反应。结果(1)临床疗效:完全缓解0例,部分缓解20例(34.48%),稳定18例(31.04%),疾病进展20例(34.48%),客观缓解率(ORR)为34.48%,疾病控制率(DCR)为65.52%;中位无进展生存期(mPFS)为4.20个月(95%CI:3.62~4.78),中位总生存期(mOS)为11.60个月(95%CI:7.99~15.21)。(2)单因素分析显示:体力状况评分(PS)、基础疾病与DCR、mPFS及mOS均有相关性,非敏感基因突变、远处转移与mPFS、mOS均有相关性(P<0.05)。(3)多因素分析显示:PS评分、基础疾病是mPFS、mOS的影响因素(P<0.05)。(4)不良反应:腹泻58例(100.00%)、皮疹44例(75.86%),3级不良反应中腹泻7例(12.07%)、皮疹5例(8.62%),无3级以上不良事件。结论阿法替尼是晚期肺鳞癌患者二线治疗的可选择方案,疗效好,不良反应可控。
ObjectiveTo observe the efficacy and adverse reactions of afatinib in the second-line treatment of patients with advanced lung squamous cell carcinoma,and to explore the clinical value.MethodsA total of 58 patients with advanced lung squamoma with negative driver genes were collected from the First Affiliated Hospital of Bengbu Medical University from March 2020 to October 2022 and afatinib was given orally at 40 mg/d according to the guidelines.When grade 3 or more side reactions occurred,the drug was stopped until the patients recovered,and the dose of readministration was reduced by 10 mg/time to the lowest 20 mg/d.The patients were evaluated every 6 weeks according to response evaluation criteria in solid tumor 1.1 until the disease progressed,and the therapeutic efficacy and adverse effects were observed.Results(1)Clinical efficacy:0 cases of complete remission,20 cases of partial remission(34.48%),18 cases of stable disease(31.04%),20 cases of progressive disease(34.48%),objective response rate(ORR)was 34.48%,disease control rate(DCR)65.52%;The median progressionfree survival(mPFS)was 4.20 months(95%CI:3.62-4.78)and the median overall survival(mOS)was 11.60 months(95%CI:7.99-15.21).(2)Univariate results showed that PS score and underlying diseases were correlated with DCR,mPFS,and mOS,while nonsensitive gene mutation and distant metastasis were correlated with mPFS and mOS,and the differences were statistically significant(P<0.05).(3)Multiple factors showed that PS score and underlying disease were risk factors for mPFS and mOS,and the differences were statistically significant(P<0.05).(4)Adverse reactions:diarrhea in 58 cases(100.00%),skin rash in 44 cases(75.86%),and grade 3 adverse reactions,diarrhea in 7 cases(12.07%),skin rash in 5 cases(8.62%),no grade 3 or above adverse events.ConclusionAfatinib is an alternative second-line treatment for patients with advanced lung squamous cell carcinoma,with good efficacy and controllable side effects.
作者
刘允
刘莹
刘佳慧
王璐
侯文瑞
李殿明
LIU Yun;LIU Ying;LIU Jiahui;WANG Lu;HOU Wenrui;LI Dianming(Department of Respiratory and Critical Medicine,the First Affiliated Hospital of Bengbu Medical University,Bengbu,Anhui 233004,China)
出处
《中华全科医学》
2024年第9期1491-1495,1499,共6页
Chinese Journal of General Practice
基金
安徽省教育厅自然科学研究重点项目(KJ2018A0997)
蚌埠医学院自然科学研究重点项目(2020byzd120)。
关键词
肺鳞癌
阿法替尼
靶向治疗
疗效
Lung squamous cell carcinoma
Afatinib
Targeted therapy
Curative effect