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非小细胞肺癌中间变性淋巴瘤激酶和表皮生长因子受体突变的免疫组织化学研究

An Immunohistochemical Study of Anaplastic Lymphoma Kinase and Epidermal Growth Factor Receptor Mutation in Non-Small Cell Lung Carcinoma.

作者信息

Verma Sonal, Kumar Madhu, Kumari Malti, Mehrotra Raj, Kushwaha R A S, Goel Madhumati, Kumar Ashutosh, Kant Surya

机构信息

Senior Resident, Department of Pathology, King George's Medical University, Lucknow, Uttar Pradesh, India.

Associate Professor, Department of Pathology, King George's Medical University, Lucknow, Uttar Pradesh, India.

出版信息

J Clin Diagn Res. 2017 Jul;11(7):EC22-EC25. doi: 10.7860/JCDR/2017/27941.10279. Epub 2017 Jul 1.

Abstract

INTRODUCTION

Lung cancer is one of the leading causes of cancer related death. Targeted treatment for specific markers may help in reducing the cancer related morbidity and mortality.

AIM

To study expression of Anaplastic Lymphoma Kinase (ALK)and Epidermal Growth Factor Receptor (EGFR) mutations in patients of Non-Small Cell Lung Cancer NSCLC, that are the targets for specific ALK inhibitors and EGFR tyrosine kinase inhibitors.

MATERIALS AND METHODS

Total 69 cases of histologically diagnosed NSCLC were examined retrospectively for immunohistochemical expression of EGFR and ALK, along with positive control of normal placental tissue and anaplastic large cell lymphoma respectively.

RESULTS

Of the NSCLC, Squamous Cell Carcinoma (SCC) accounted for 71.0% and adenocarcinoma was 26.1%. ALK expression was seen in single case of 60-year-old female, non-smoker with adenocarcinoma histology. EGFR expression was seen in both SCC (59.18%) and adenocarcinoma in (77.78%) accounting for 63.77% of all cases. Both ALK and EGFR mutation were mutually exclusive.

CONCLUSION

EGFR expression was seen in 63.77% of cases, highlighting the importance of its use in routine analysis, for targeted therapy and better treatment results. Although, ALK expression was seen in 1.45% of all cases, it is an important biomarker in targeted cancer therapy. Also, the mutually exclusive expression of these two markers need further studies to develop a diagnostic algorithm for NSCLC patients.

摘要

引言

肺癌是癌症相关死亡的主要原因之一。针对特定标志物的靶向治疗可能有助于降低癌症相关的发病率和死亡率。

目的

研究间变性淋巴瘤激酶(ALK)和表皮生长因子受体(EGFR)突变在非小细胞肺癌(NSCLC)患者中的表达情况,这两种标志物分别是特定ALK抑制剂和EGFR酪氨酸激酶抑制剂的作用靶点。

材料与方法

回顾性检查69例经组织学诊断为NSCLC的患者,检测EGFR和ALK的免疫组化表达情况,同时分别以正常胎盘组织和间变性大细胞淋巴瘤作为阳性对照。

结果

在NSCLC中,鳞状细胞癌(SCC)占71.0%,腺癌占26.1%。ALK表达见于1例60岁女性非吸烟腺癌患者。EGFR表达在SCC中占59.18%,在腺癌中占77.78%,占所有病例的63.77%。ALK和EGFR突变相互排斥。

结论

63.77%的病例检测到EGFR表达,凸显了其在常规分析、靶向治疗及改善治疗效果方面的重要性。虽然所有病例中ALK表达仅占1.45%,但它是靶向癌症治疗中的一个重要生物标志物。此外,这两种标志物的相互排斥表达情况需要进一步研究,以开发针对NSCLC患者的诊断算法。

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