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可手术治疗的鳞状细胞喉癌中胰岛素样生长因子 1 受体(IGF1R)的表达与生存。

Insulin-like growth factor 1 receptor (IGF1R) expression and survival in operable squamous-cell laryngeal cancer.

机构信息

Department of Medical Oncology, 251 Airforce General Hospital, Athens, Greece.

出版信息

PLoS One. 2013;8(1):e54048. doi: 10.1371/journal.pone.0054048. Epub 2013 Jan 24.

Abstract

INTRODUCTION

Prognosis of patients with operable laryngeal cancer is highly variable and therefore potent prognostic biomarkers are warranted. The insulin-like growth factor receptor (IGFR) signaling pathway plays a critical role in laryngeal carcinogenesis and progression.

PATIENTS AND METHODS

We identified all patients with localized TNM stage I-III laryngeal cancer managed with potentially curative surgery between 1985 and 2008. Immunohistochemical (IHC) expression of IGF1R-alpha, IGF1R-beta and IGF2R was evaluated using the immunoreactive score (IRS) and mRNA levels of important effectors of the IGFR pathway were assessed, including IGF1R, IGF-binding protein 3 (IGFBP3), suppressor of cytokine signaling 2 (SOCS2) and members of the MAP-kinase (MAP2K1, MAPK9) and phosphatidyl-inositol-3 kinase (PIK3CA, PIK3R1) families. Cox-regression models were applied to assess the predictive value of biomarkers on disease-free survival (DFS) and overall survival (OS).

RESULTS

Among 289 eligible patients, 95.2% were current or ex smokers, 75.4% were alcohol abusers, 15.6% had node-positive disease and 32.2% had received post-operative irradiation. After a median follow-up of 74.5 months, median DFS was 94.5 months and median OS was 106.3 months. Using the median IRS as the pre-defined cut-off, patients whose tumors had increased IGF1R-alpha cytoplasm or membrane expression experienced marginally shorter DFS and significantly shorter OS compared to those whose tumors had low IGF1R-alpha expression (91.1 vs 106.2 months, p = 0.0538 and 100.3 vs 118.6 months, p = 0.0157, respectively). Increased mRNA levels of MAPK9 were associated with prolonged DFS (p = 0.0655) and OS (p = 0.0344). In multivariate analysis, IGF1R-alpha overexpression was associated with a 46.6% increase in the probability for relapse (p = 0.0374). Independent predictors for poor OS included node-positive disease (HR = 2.569, p<0.0001), subglottic/transglottic localization (HR = 1.756, p = 0.0438) and IGF1R-alpha protein overexpression (HR = 1.475, p = 0.0504).

CONCLUSION

IGF1R-alpha protein overexpression may serve as an independent predictor of relapse and survival in operable laryngeal cancer. Prospective evaluation of the IGF1R-alpha prognostic utility is warranted.

摘要

简介

可手术喉癌患者的预后差异很大,因此需要强有力的预后生物标志物。胰岛素样生长因子受体(IGF1R)信号通路在喉癌的发生和发展中起着关键作用。

患者和方法

我们确定了 1985 年至 2008 年间接受潜在治愈性手术治疗的局限性 TNM Ⅰ-Ⅲ期喉癌的所有患者。使用免疫反应评分(IRS)评估 IGF1R-α、IGF1R-β 和 IGF2R 的免疫组化(IHC)表达,并评估 IGF1R 途径的重要效应物的 mRNA 水平,包括 IGF1R、IGF 结合蛋白 3(IGFBP3)、细胞因子信号转导抑制因子 2(SOCS2)以及丝裂原活化蛋白激酶(MAP2K1、MAPK9)和磷脂酰肌醇-3 激酶(PIK3CA、PIK3R1)家族成员。应用 Cox 回归模型评估生物标志物对无病生存率(DFS)和总生存率(OS)的预测价值。

结果

在 289 名合格患者中,95.2%为现吸烟者或既往吸烟者,75.4%为酗酒者,15.6%为淋巴结阳性疾病,32.2%接受了术后放疗。中位随访 74.5 个月后,中位 DFS 为 94.5 个月,中位 OS 为 106.3 个月。使用中位数 IRS 作为预设的截止值,与 IGF1R-α 表达水平低的患者相比,IGF1R-α 细胞质或膜表达增加的患者的 DFS 略有缩短,OS 显著缩短(91.1 对 106.2 个月,p = 0.0538 和 100.3 对 118.6 个月,p = 0.0157)。MAPK9 mRNA 水平升高与 DFS 延长相关(p = 0.0655)和 OS(p = 0.0344)。多变量分析显示,IGF1R-α 过表达与复发概率增加 46.6%相关(p = 0.0374)。OS 不良的独立预测因素包括淋巴结阳性疾病(HR = 2.569,p<0.0001)、声门下/跨声门定位(HR = 1.756,p = 0.0438)和 IGF1R-α 蛋白过表达(HR = 1.475,p = 0.0504)。

结论

IGF1R-α 蛋白过表达可能是可手术喉癌复发和生存的独立预测因子。需要前瞻性评估 IGF1R-α 的预后实用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24ed/3554755/6ee7b5f2f044/pone.0054048.g001.jpg

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