HER2、Ki67和p53在骨肉瘤中的共存:一个强有力的预后因素。

Keykhosro Mardanpour, Mahtab Rahbar, Sourena Mardanpour
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引用次数: 31

摘要

背景:许多实验室目前正在评估使用免疫组织化学技术测定人表皮生长因子受体2 (HER2)、p53和Ki67增殖指标在癌症中的有效性。尽管现有的研究表明,这些因素可能确实有助于骨肉瘤患者的治疗决策,但其临床有效性仍存在争议。目的:我们提出HER2过表达、p53蛋白积累和Ki67在骨肉瘤中共存的价值,这可能是骨肉瘤的一个预后因素。材料与方法:采用免疫组化方法检测2009 - 2014年56例骨肉瘤患者(中位随访时间为48个月)骨肿瘤切除组织标本中HER2、p53、Ki67的表达,并分析其对预后的意义。结果:56例成骨肉瘤组织样本中,HER2过表达阳性占80%,p53蛋白积累阳性占89%,Ki67表达阳性占96.5%。HER2过表达和p53蛋白积累与降低无病生存率(P < 0.01)和总生存率(P < 0.003)显著相关。HER2和Ki67共过表达与降低无病(P < 0.03)和总生存率(P < 0.02)显著相关。HER2、p53蛋白积累、Ki67共过表达与随访时间内肿瘤大小较大、肿瘤分级高、淋巴结阳性、转移的患者无病生存率(P < 0.01)、总生存率(P < 0.005)显著相关。结论:我们发现HER2和Ki67过表达和p53蛋白积累共存的证据预测了高级别骨肉瘤患者淋巴结累及和转移的发展,并与生存率降低显著相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Coexistence of HER2, Ki67, and p53 in Osteosarcoma: A Strong Prognostic Factor.

Coexistence of HER2, Ki67, and p53 in Osteosarcoma: A Strong Prognostic Factor.

Coexistence of HER2, Ki67, and p53 in Osteosarcoma: A Strong Prognostic Factor.

Coexistence of HER2, Ki67, and p53 in Osteosarcoma: A Strong Prognostic Factor.

Background: Many laboratories are currently evaluating the usefulness of the determination of human epidermal growth factor receptor 2 (HER2), p53, and Ki67 proliferation indices using immunohistochemical techniques in cancer. Although the available studies suggest that these factors might indeed be helpful in making treatment decisions in osteosarcoma patients, their clinical usefulness is still controversial.

Aims: We proposed to introduce the value of the coexistence of HER2 overexpression, p53 protein accumulation, and Ki67 in osteosarcoma, which could be a prognostic factor in osteosarcoma.

Material and methods: Expression of HER2, p53, and Ki67 was examined by immunohistochemistry in samples of resected bone tumor tissue from 56 patients with osteosarcoma, obtained between 2009 and 2014 (median follow-up period of 48 months), and their significance for prognosis was analyzed.

Results: Of the 56 osteogenic sarcoma tissue samples, 80, 89, and 96.5% were positive for HER2 overexpression, p53 protein accumulation, and Ki67 expression, respectively. Overexpression of HER2 and accumulation of p53 protein significantly correlated with reduced disease-free (P < 0.01) and overall survival (P < 0.003). HER2 and Ki67 co-overexpression significantly correlated with decreased disease-free (P < 0.03) and overall survival (P < 0.02). HER2, accumulation of p53 protein, and Ki67 co-overexpression significantly correlated with reduced disease-free (P < 0.01) and overall survival (P < 0.005) as did patients with larger tumor size, high grade of tumor, positive lymph node, and metastasis status within the specified period of follow up.

Conclusions: We found evidence that coexistence of HER2 and Ki67 overexpression and p53 protein accumulation predict the development of lymph node involvement and metastases in patients with high-grade osteosarcoma and were significantly associated with reduced survival.

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