Alectinib/Crizotinib一线治疗Alectinib预后不佳的无定形淋巴瘤激酶阳性非小细胞肺癌患者的数据比较。

0 RESPIRATORY SYSTEM
Nuran Katgı, Pınar Çimen, Murat Akyol, Pınar Gürsoy, Nurşin Agüloğlu
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引用次数: 0

摘要

目的:在被诊断为间变性淋巴瘤激酶突变阳性的非小细胞肺癌患者中,阿来替尼比克唑替尼具有更好的中枢神经系统传播。我们的目的是调查阿来替尼在治疗中的疗效及其在一线治疗中的地位,并报告我们的真实数据。材料和方法:回顾性分析2016年至2021年间在我们诊所诊断为间变性淋巴瘤激酶阳性非小细胞肺癌的38名患者的数据,这些患者之前没有接受任何治疗。结果:在接受阿来替尼治疗的19名患者中,14名患者有多发性脑转移,6名患者在治疗前有脑转移。在治疗期间未发现新出现的脑转移瘤。患者的无进展生存期为23.5±4.2个月,总生存期为24.6±4.1个月。在10名(52.6%)患者中观察到进展。在接受克唑替尼治疗的19名患者中,7名患者有多发性转移,1名患者在治疗前和6名患者在疗程中检测到脑转移。克唑替尼患者的无进展生存期为17.1±4.8个月,总生存期为26.5±6.1个月。在17名(89.5%)患者中观察到进展。其中8名患者可服用第二种阿来替尼。阿来替尼二线治疗后的总生存期为18.2±7.0个月。不能接受阿来替尼二线治疗的患者的总生存期为4.0±2.0个月。结论:阿来替尼组的进展率低于克唑替尼组,尽管阿来替尼组有更多的多发转移和脑转移患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Comparison of Alectinib/Crizotinib Data in First-Line Therapy in Patients with Anaplastic LymphomakinasePositive Nonsmall Cell Lung Carcinoma with Poor Prognostic Features for Alectinib.

Comparison of Alectinib/Crizotinib Data in First-Line Therapy in Patients with Anaplastic LymphomakinasePositive Nonsmall Cell Lung Carcinoma with Poor Prognostic Features for Alectinib.

Objective: Alectinib has a much better central nervous system transmission than crizotinib in patients diagnosed with anaplastic lymphoma kinase mutation-positive nonsmall cell lung carcinoma. We aimed to investigate alectinib's efficacy in the treatment and its place in the first-line treatment and report our real-life data.

Material and methods: The data of 38 patients who were diagnosed with anaplastic lymphoma kinase-positive nonsmall cell lung carcinoma in our clinic between 2016 and 2021, who did not receive any treatment before were retrospectively analyzed.

Results: Of the 19 patients who received alectinib, 14 had multiple, and 6 had pretreatment brain metastases. No newly emerging brain metastases were detected during the treatment period. The progression-free survival of patients was 23.5 ± 4.2 months, and overall survival was 24.6 ± 4.1 months. Progression was observed in 10 (52.6%) patients. Of the 19 patients who received crizotinib, 7 had multiple metastases, and brain metastases were detected in 1 patient before treatment and 6 patients during the treatment period. Progression-free survival of crizotinib patients was 17.1 ± 4.8 months and their overall survival was 26.5 ± 6.1 months. Progression was observed in 17 (89.5%) patients. The second line of alectinib could be given to 8 of these patients. Overall survival after second-line treatment of alectinib was 18.2 ± 7.0 months. Overall survival of the patients who could not receive second-line treatment of alectinib was 4.0 ± 2.0 months.

Conclusion: The progression rate was lower in alectinib than the crizotinib patients, although there were more patients with multiple metastases and brain metastases in the alectinib arm.

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