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原肌球蛋白受体激酶A在默克尔细胞癌细胞上的表达。

Tropomyosin Receptor Kinase A Expression on Merkel Cell Carcinoma Cells.

作者信息

Wehkamp Ulrike, Stern Sophie, Krüger Sandra, Hauschild Axel, Röcken Christoph, Egberts Friederike

机构信息

Department of Dermatology, University Hospital Schleswig-Holstein, Kiel, Germany.

Department of Pathology, University Hospital Schleswig-Holstein, Kiel, Germany.

出版信息

JAMA Dermatol. 2017 Nov 1;153(11):1166-1169. doi: 10.1001/jamadermatol.2017.2495.

Abstract

IMPORTANCE

Merkel cell carcinoma (MCC) is a malignant neuroendocrine skin tumor frequently associated with the Merkel cell polyomavirus. Immune checkpoint therapy showed remarkable results, although not all patients are responsive to this therapy. Anti-tropomyosin receptor kinase A (TrkA)-targeted treatment has shown promising results in several tumor entities.

OBJECTIVE

To determine TrkA expression in MCC as a rationale for potential targeted therapy.

DESIGN, SETTING, AND PARTICIPANTS: This case series study investigated the MCC specimens of 55 patients treated at the Department of Dermatology, University Hospital of Schleswig-Holstein, Kiel, Germany, from January 1, 2005, through December 31, 2015. Thirty-nine of the 55 samples were suitable for further histopathologic examination. Expression of TrkA was explored by immunohistochemical analysis.

EXPOSURE

Diagnosis of MCC was confirmed by staining positive for cytokeratin 20 (CK20) and synaptophysin.

MAIN OUTCOMES AND MEASURES

Expression of TrkA on the tumor cells.

RESULTS

Specimens of 39 patients (21 women and 18 men; mean [SD] age, 75.0 [7.8] years) underwent immunohistochemical investigation. Thirty-eight of 38 specimens expressed CK20 and synaptophysin on the MCC tumor cells (100% expression). Merkel cell polyomavirus was detected in 32 of 38 specimens (84%). Tropomyosin receptor kinase A was found in all 36 evaluable specimens on the tumor cells; 34 (94%) showed a weak and 2 (6%) showed a strong cytoplasmic expression. In addition, strongly positive perinuclear dots were observed in 30 of 36 specimens (83%).

CONCLUSIONS AND RELEVANCE

Tropomyosin receptor kinase A was expressed on MCC tumor cells in 100% of evaluable specimens. This result may lead to the exploration of new targeted treatment options in MCC, especially for patients who do not respond to anti-programmed cell death protein 1 treatment.

摘要

重要性

默克尔细胞癌(MCC)是一种恶性神经内分泌性皮肤肿瘤,常与默克尔细胞多瘤病毒相关。免疫检查点疗法显示出显著效果,尽管并非所有患者都对该疗法有反应。抗原肌球蛋白受体激酶A(TrkA)靶向治疗在多个肿瘤实体中已显示出有前景的结果。

目的

确定MCC中TrkA的表达情况,作为潜在靶向治疗的理论依据。

设计、背景和参与者:本病例系列研究调查了2005年1月1日至2015年12月31日期间在德国基尔石勒苏益格 - 荷尔斯泰因大学医院皮肤科接受治疗的55例患者的MCC标本。55个样本中有39个适合进一步的组织病理学检查。通过免疫组织化学分析探索TrkA的表达。

暴露

通过细胞角蛋白20(CK20)和突触素染色阳性确诊为MCC。

主要结局和测量指标

肿瘤细胞上TrkA的表达。

结果

对39例患者(21名女性和18名男性;平均[标准差]年龄,75.0[7.8]岁)的标本进行了免疫组织化学研究。38个标本中的38个在MCC肿瘤细胞上表达CK20和突触素(表达率100%)。38个标本中的32个(84%)检测到默克尔细胞多瘤病毒。在所有36个可评估标本的肿瘤细胞中均发现了原肌球蛋白受体激酶A;其中34个(94%)显示弱细胞质表达,2个(6%)显示强细胞质表达。此外,36个标本中的30个(83%)观察到强阳性核周点。

结论及相关性

在100%的可评估标本中,原肌球蛋白受体激酶A在MCC肿瘤细胞上表达。这一结果可能会促使探索MCC新的靶向治疗方案,特别是对于那些对抗程序性细胞死亡蛋白1治疗无反应的患者。

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