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非小细胞肺癌患者可溶性表皮生长因子受体(sEGFR)和癌胚抗原(CEA)浓度:与厄洛替尼和吉非替尼治疗后生存的相关性

Soluble epidermal growth factor receptor (sEGFR) and carcinoembryonic antigen (CEA) concentration in patients with non-small cell lung cancer: correlation with survival after erlotinib and gefitinib treatment.

作者信息

Kappers I, Vollebergh M A, van Tinteren H, Korse C M, Nieuwenhuis L L, Bonfrer J M G, Klomp H M, van Zandwijk N, van den Heuvel M M

机构信息

Department of Surgery.

出版信息

Ecancermedicalscience. 2010;4:178. doi: 10.3332/ecancer.2010.178. Epub 2010 Nov 3.

Abstract

BACKGROUND

In patients with non-small cell lung cancer (NSCLC), a higher response rate can be achieved with epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs) when selection for therapy is guided by mutation analysis or gene amplification. However, both tests are complex and require tumour tissue. Simple methods to identify responders prior to EGFR-TKI treatment are urgently needed. This study aimed to define the relation between serum sEGFR levels, carcinoembryonic antigen (CEA) and survival in NSCLC patients treated with EGFR-TKIs.

METHODS

Patients with stage III/IV NSCLC treated with gefitinib or erlotinib between July 2002 and December 2005 were reviewed. Levels of serum soluble EGFR (sEGFR) were determined by a sandwich quantitative enzyme-linked immunosorbent assay. A chemiluminescence immunoassay was used for CEA. The relation between sEGFR and survival was investigated.

RESULTS

One hundred and two NSCLC patients, mainly stage IV (80%), were identified. Mean sEGFR at baseline was 55.9 μg/l (range 35.3-74.5 μg/l). The median CEA level was 11.1 μg/l (range <1.0-2938.0 μg/l). Median overall survival was 5.2 months (range 1-52 months). Decreasing log CEA values (HR 1.51, 95% CI 1.11-2.04, multivariate analysis) and increasing sEGFR values (HR 0.96, 95% CI 0.93-0.99, multivariate analysis) were both independently associated with prolonged survival. Higher levels of pre-treatment sEGFR were associated with lower risk of progressive disease within three months (p=0.04).

CONCLUSIONS

Both baseline sEGFR and CEA levels in NSCLC patients receiving EGFR-TKIs showed a significant correlation with survival. To distinguish whether these factors have a predictive or a prognostic value, validation is warranted in an independent patient series containing a control arm without EGFR-TKI treatment.

摘要

背景

在非小细胞肺癌(NSCLC)患者中,当根据突变分析或基因扩增指导治疗选择时,表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)可实现更高的缓解率。然而,这两种检测都很复杂且需要肿瘤组织。迫切需要在EGFR-TKI治疗前识别反应者的简单方法。本研究旨在确定血清可溶性EGFR(sEGFR)水平、癌胚抗原(CEA)与接受EGFR-TKIs治疗的NSCLC患者生存率之间的关系。

方法

回顾了2002年7月至2005年12月期间接受吉非替尼或厄洛替尼治疗的III/IV期NSCLC患者。采用夹心定量酶联免疫吸附测定法测定血清可溶性EGFR(sEGFR)水平。癌胚抗原(CEA)检测采用化学发光免疫分析法。研究了sEGFR与生存率之间的关系。

结果

共纳入102例NSCLC患者,主要为IV期(80%)。基线时sEGFR的平均值为55.9μg/l(范围35.3 - 74.5μg/l)。CEA水平中位数为11.1μg/l(范围<1.0 - 2938.0μg/l)。总生存期中位数为5.2个月(范围1 - 52个月)。CEA值对数降低(多因素分析中HR 1.51,95%CI 1.11 - 2.04)和sEGFR值升高(多因素分析中HR 0.96,95%CI 0.93 - 0.99)均与生存期延长独立相关。治疗前sEGFR水平较高与三个月内疾病进展风险较低相关(p = 0.04)。

结论

接受EGFR-TKIs治疗的NSCLC患者的基线sEGFR和CEA水平均与生存率显著相关。为了区分这些因素是具有预测价值还是预后价值,有必要在一个包含未接受EGFR-TKI治疗的对照组的独立患者系列中进行验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6886/3234018/9a51b043caa1/can-4-178f1.jpg

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