盐酸安洛替尼胶囊治疗晚期非小细胞肺癌的临床疗效分析

Yitan Zou, Fang Ning, Jingxi Zhang, Yi Huang, Yiping Han, Li-jun Zhao, Yuchao Dong, C. Bai
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引用次数: 0

摘要

目的观察盐酸安洛替尼胶囊治疗晚期非小细胞肺癌(NSCLC)的疗效及毒副反应。方法收集2018年6月至2019年3月海军医科大学附属长海医院诊断为ⅢB期至Ⅳ期晚期NSCLC并接受盐酸安洛替尼胶囊治疗的35例患者的临床资料。所有患者既往均接受1 - 2线标准治疗,随访时间截止至2019年3月31日。结果35例患者无完全缓解或部分缓解,病情稳定19例(54.3%),病情进展16例(45.7%)。ORR为0%,DCR为54.3%。临床疗效与EGFR、ROS1突变、PD1、PDL1、p53、KI67表达情况、性别、病理类型、分期、年龄、PS评分无关。非吸烟组的中位PFS高于吸烟组[M(QR): 3.3(2.0)个月vs 2.0(1.5)个月],差异有统计学意义(Z=1.23, P<0.05)。脑转移组的中位PFS低于无脑转移组[M(QR): 3.7(2.9)个月vs 6.5(2.0)个月],差异有统计学意义(Z=-2.21, P<0.05)。不良反应组的中位PFS高于无不良反应组[M(QR): 3.6(1.9)个月vs 2.3(1.7)个月],差异有统计学意义(Z=-2.07, P<0.05)。不良反应包括高血压4例(11.42%)、手足综合征6例(17.14%)、胃肠道反应5例(14.28%)、肾虚1例(2.85%)、气胸1例(2.85%)、口腔溃疡3例(8.57%)、声音嘶哑4例(11.42%)。结论盐酸安洛替尼治疗晚期NSCLC具有一定的疗效,且在非吸烟患者、无脑转移组和有不良反应患者中疗效更优。经对症治疗,不良反应可耐受。盐酸安洛替尼在晚期NSCLC患者中具有特殊的临床应用价值。关键词:肺癌,非小细胞肺;治疗效果;Anlotinib盐酸盐;血管内皮生长因子激酶抑制剂;不良反应
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Analysis of the clinical effect of Anlotinib hydrochloride capsules in the treatment of advanced non-small cell lung cancer patients
Objective To observe the curative effects and toxic side effects of Anlotinib hydrochloride capsules in the treatment of advanced non-small cell lung cancer (NSCLC). Methods Clinical data was collected from 35 patients who were diagnosed of phase ⅢB to Ⅳ advanced NSCLC and were treated with Anlotinib hydrochloride capsules during June 2018 to March 2019 in Changhai Hospital Affiliated to Naval Medical University.All these patients had been treated with one or two lines of standard prior treatments and the follow-up time was cut off until March 31st, 2019. Results No case achieved complete response or partial response, 19 cases (54.3%)achieved stable disease and 16(45.7%) achieved progressive disease in 35 cases.The ORR was 0% and the DCR was 54.3%.The clinical effect was not related with the following factors including the mutation of EGFR and ROS1, the expression status of PD1, PDL1, p53 and KI67, gender, pathology type, stage, age and PS score.The median PFS of non-smoking group was higher than that of the smoking group [M(QR): 3.3(2.0) months vs 2.0(1.5) months] and the difference was statistically significant (Z=1.23, P<0.05). The median PFS of group with brain metastasis was lower than that of group without brain metastasis [M(QR): 3.7(2.9) months vs 6.5(2.0) months] and the difference was statistically significant (Z=-2.21, P<0.05). The median PFS of group with adverse reactions was higher than that of group without adverse reactions [M(QR): 3.6(1.9) months vs 2.3(1.7) months] and the difference was statistically significant (Z=-2.07, P<0.05). Adverse reactions included 4 cases of hypertension (11.42%), 6 case of hand-foot syndrome (17.14%), 5 case of gastrointestinal reaction (14.28%), 1 case of renal deficiency (2.85%), 1 case of pneumothorax (2.85%), 3 cases of oral ulcer (8.57%) and 4 cases of hoarseness (11.42%). Conclusions Anlotinib hydrochloride in the treatment of advanced NSCLC has certain therapeutic effect, which is superior in non-smoking patients, group without brain metastasis and patients suffering adverse reactions.The adverse reactions can be tolerated after symptomatic treatment.Anlotinib hydrochloride has special clinical application value in patients with advanced NSCLC. Key words: Carcinoma, non-small-cell lung; Treatment outcome; Anlotinib hydrochloride; Vascular endothelial growth factor-kinase inhibitor; Adverse reaction
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