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编码半胱天冬酶8的基因多态性可能预测局部晚期或晚期非小细胞肺癌一线铂类化疗的疗效。

Polymorphisms in the Gene Encoding Caspase 8 May Predict the Response to First-Line Platinum-Based Chemotherapy in Locally Advanced or Advanced Non-Small-Cell Lung Cancer.

作者信息

Szczyrek Michał, Mlak Radosław, Szudy-Szczyrek Aneta, Kędziora Karolina, Małecka-Massalska Teresa, Krawczyk Paweł, Milanowski Janusz

机构信息

Department of Pneumonology, Oncology and Allergology, Medical University of Lublin, 20-090 Lublin, Poland.

Department of Human Physiology, Medical University of Lublin, 20-080 Lublin, Poland.

出版信息

J Clin Med. 2021 Mar 8;10(5):1126. doi: 10.3390/jcm10051126.

DOI:10.3390/jcm10051126
PMID:33800294
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7962636/
Abstract

Caspase 8 is a protein involved in the process of cell apoptosis, which may affect the efficacy of anti-cancer treatment. The aim of our study was to determine the impact of polymorphisms in the gene encoding caspase 8 on the prognosis in non-small-cell lung cancer (NSCLC). The study involved 99 patients with newly diagnosed locally advanced or metastatic NSCLC treated with platinum-based chemotherapy. The presence of the GG genotype was associated with distant metastases, smoking, and a family history of cancer. The higher risk of early progression was associated with weight loss and the genotype (GG vs. AG or AA: 20.51% vs. 2.86%). The higher risk of progression-free survival (PFS) shortening was associated with a higher stage of disease (hazard ratio (HR) = 2.50, 95% CI: 1.61-3.89, < 0.0001), distant metastases (HR = 2.30, 95% CI: 1.42-3.72, = 0.0016), and the GG genotype (HR = 1.68, 95% CI: 1.10-2.57, = 0.0152). The influence of the GG genotype on the PFS was confirmed in a multivariate analysis (HR = 1.80, 95% CI: 1.06-3.05, = 0.0317). We did not confirm the influence of genotypes on the overall survival (OS).

摘要

半胱天冬酶8是一种参与细胞凋亡过程的蛋白质,它可能会影响抗癌治疗的疗效。我们研究的目的是确定编码半胱天冬酶8的基因多态性对非小细胞肺癌(NSCLC)预后的影响。该研究纳入了99例新诊断的局部晚期或转移性NSCLC患者,他们接受了铂类化疗。GG基因型的存在与远处转移、吸烟和癌症家族史有关。早期进展的较高风险与体重减轻和该基因型有关(GG与AG或AA相比:20.51%对2.86%)。无进展生存期(PFS)缩短的较高风险与疾病分期较高(风险比(HR)=2.50,95%置信区间:1.61-3.89,P<0.0001)、远处转移(HR = 2.30,95%置信区间:1.42-3.72,P = 0.0016)和GG基因型(HR = 1.68,95%置信区间:1.10-2.57,P = 0.0152)有关。GG基因型对PFS的影响在多变量分析中得到证实(HR = 1.80,95%置信区间:1.06-3.05,P = 0.0317)。我们未证实基因型对总生存期(OS)的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db0c/7962636/0b7757c97d8e/jcm-10-01126-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db0c/7962636/c24bd1959963/jcm-10-01126-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db0c/7962636/0b7757c97d8e/jcm-10-01126-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db0c/7962636/c24bd1959963/jcm-10-01126-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db0c/7962636/0b7757c97d8e/jcm-10-01126-g002.jpg

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