非转移性乳腺癌患者的临床病理参数和生存数据与肿瘤浸润淋巴细胞、雄激素受体和胰岛素样生长因子受体1表达的关系

JM Njenga, A. El-Gowily, W. Arafat, D. Abdalla, Y. Rostom
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Chi square and Kaplan Meier curves were used to study the correlation between the three biomarkers and clinicopathologic parameters and survival respectively. Results: 59% and 51.4% of patients were AR and IGF-1R positive respectively. AR immunoreactivity correlated with a tumour size less than 5 centimeters (p=0.001), presence of carcinoma in situ (p=0.008), negative Her 2 status (p=0.007) and negative lymphovascular invasion (p<0.001). Negative AR expression predicted a longer disease free survival (p=0.017). A positive IGF-1R was associated with carcinoma in situ (p<0.001) and negative extra-nodal extension (p=0.042) but no impact on the disease free survival (p=0.227). A high TIL expression was associated with a tumour size less than 5 centimeters (p=0.005), invasive lobular carcinoma (p=0.006), carcinoma in situ (p=0.047), negative LVI (p<0.001) and longer survival. A positive AR expression was associated with a positive IGF-1R expression (p<0.001). 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引用次数: 0

摘要

导言:乳腺癌(BC)的不断演变的性质使得识别和评估更多可能具有预测和预后价值的生物标志物变得至关重要。我们探讨了雄激素受体(AR)、胰岛素样生长因子1受体(IGF-1R)和肿瘤浸润淋巴细胞(TILs)与BC患者临床病理变量和生存率之间的关系。材料与方法:本回顾性研究收集2010年1月至2016年12月在亚历山大大学附属医院治疗的105例BC患者的临床和病理资料。提取这些患者的福尔马林固定石蜡包埋块,免疫组织化学分析AR和IGF-1R的表达;苏木精和伊红染色评价TILs。采用卡方曲线和Kaplan Meier曲线分别研究3种生物标志物与临床病理参数和生存率的相关性。结果:59%的患者AR阳性,51.4%的患者IGF-1R阳性。AR免疫反应性与肿瘤大小小于5厘米(p=0.001)、原位癌存在(p=0.008)、Her 2阴性(p=0.007)和淋巴血管浸润阴性(p<0.001)相关。AR阴性表达预示着更长的无病生存期(p=0.017)。IGF-1R阳性与原位癌(p<0.001)和淋巴结外延伸阴性(p=0.042)相关,但对无病生存无影响(p=0.227)。TIL高表达与肿瘤大小小于5厘米(p=0.005)、浸润性小叶癌(p=0.006)、原位癌(p=0.047)、LVI阴性(p<0.001)和较长的生存期相关。AR阳性表达与IGF-1R阳性表达相关(p<0.001)。结论:AR、IGF-1R和TILs与BC中使用的各种临床病理变量有不同的相关性;此外,它们都具有预测价值。这两种受体是BC的一个有希望的靶点。需要更多的临床研究来进一步证实这三种生物标志物的效用。
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Clinicopathologic Parameters and Survival Data in Non-Metastatic Breast Cancer Patients in Correlation with Tumour Infiltrating Lymphocytes, Androgen Receptor and Insulin-Like Growth Factor Receptor 1 Expression
Introduction: The constantly evolving nature of breast cancer (BC) makes it paramount to identify and evaluate more biomarkers that may have a predictive and prognostic value. We explored the relationship between the androgen receptor (AR), insulin-like growth factor 1 receptor (IGF-1R) and tumour infiltrating lymphocytes (TILs), and clinicopathologic variables and survival in BC. Materials and Methods: In this retrospective study, we collected clinical and pathological data of 105 BC patients who had been treated at Alexandria Main University Hospitals from January 2010 to December 2016. These patients’ formalin fixed paraffin-embedded blocks were retrieved and analyzed for AR and IGF-1R expression immunohistochemically; TILs were assessed by hematoxylin and eosin staining. Chi square and Kaplan Meier curves were used to study the correlation between the three biomarkers and clinicopathologic parameters and survival respectively. Results: 59% and 51.4% of patients were AR and IGF-1R positive respectively. AR immunoreactivity correlated with a tumour size less than 5 centimeters (p=0.001), presence of carcinoma in situ (p=0.008), negative Her 2 status (p=0.007) and negative lymphovascular invasion (p<0.001). Negative AR expression predicted a longer disease free survival (p=0.017). A positive IGF-1R was associated with carcinoma in situ (p<0.001) and negative extra-nodal extension (p=0.042) but no impact on the disease free survival (p=0.227). A high TIL expression was associated with a tumour size less than 5 centimeters (p=0.005), invasive lobular carcinoma (p=0.006), carcinoma in situ (p=0.047), negative LVI (p<0.001) and longer survival. A positive AR expression was associated with a positive IGF-1R expression (p<0.001). Conclusions: AR, IGF-1R and TILs correlate differently with various clinicopathologic variables used in BC; in addition they all have a prognostic value. The two receptors are a promising target in BC. More clinical studies are required to further confirm the utility of these three biomarkers.
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