胃肠道间质瘤中Her2/neu表达的预后价值:免疫组织化学研究

Cancer growth and metastasis Pub Date : 2017-02-16 eCollection Date: 2017-01-01 DOI:10.1177/1179064417690543
Ahmed M Abd El-Aziz, Eman A Ibrahim, Ashraf Abd-Elmoghny, Mohammed El-Bassiouny, Zina M Laban, Somaia A Saad El-Din, Youhanna Shohdy
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引用次数: 4

摘要

背景:胃肠道间质瘤(GIST)是一种较为罕见的肿瘤类型。在埃及,它占胃肠道肿瘤的2.5%,占所有恶性肿瘤的0.3%。大多数胃肠道间质瘤都发生在胃里。目的:探讨Her2/neu免疫组化表达在GIST中的意义及其与其他组织病理指标及定期随访后肿瘤复发的关系。患者和方法:本研究为回顾性和前瞻性队列研究。该研究包括32例可切除且无远处转移的gist患者。在手术切除肿瘤并保留假包膜后进行Her2/neu免疫组化染色。结果:男性占53.1%,女性占46.9%。肿瘤分为低危组(25%)、中危组(21.9%)和高危组(53.1%)。Her2/neu在56.3%的gist中为阴性,43.7%为阳性。其表达与肿瘤危险等级(P = 0.04)、肿瘤大小(P = 0.001)、有丝分裂计数(P = 0.000)、复发风险增加(P = 0.000)显著相关。此外,肿瘤复发与肿瘤有丝分裂计数显著相关(P = .00)。kappa一致性检验显示,4个有丝分裂计数/50个高倍场(high-power fields, HPF)是肿瘤与复发更相关的临界值,敏感性83%,特异性70%,P值为0.003。结论:Her2/neu可作为GIST完全切除后肿瘤复发的独立预后指标,预测肿瘤复发的有丝分裂计数截止值为4/50 HPF。然而,更多的临床研究,更多的病例荧光原位杂交整合是值得推荐的。
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Prognostic Value of Her2/neu Expression in Gastrointestinal Stromal Tumors: Immunohistochemical Study.

Background: Gastrointestinal stromal tumor (GIST) is a relatively rare type of neoplasms. In Egypt, it represents 2.5% of gastrointestinal tumors and 0.3% of all malignancies. Most of the GISTs develop in the stomach.

Aim: To reveal the significance of Her2/neu immunohistochemical expression in GIST and its correlation with other histopathologic parameters and tumor relapse after regular follow-up.

Patients and methods: This study is a retrospective and prospective cohort. It included 32 patients with GISTs, who were resectable with no distant metastasis. Immunohistochemical staining by Her2/neu was performed after complete surgical resection of the tumors with preservation of the pseudocapsule.

Results: In total, 53.1% of cases were men and 46.9% women. Tumors were classified into low-risk (25%), intermediate-risk (21.9%), and high-risk groups (53.1%). Her2/neu expression was negative in 56.3% of GISTs and positive in 43.7%. Its expression was significantly correlated with risk grade (P = .04), tumor size (P = .001), mitotic count (P = .00), and increased risk of relapse (P = .00). Furthermore, tumor relapse was significantly correlated with the tumor mitotic counts (P = .00). Using kappa agreement test, it showed that 4 mitotic counts/50 high-power fields (HPF) was the cutoff value with which the tumor might be associated more with relapse, with 83% sensitivity, 70% specificity, and P value of .003.

Conclusions: Her2/neu might be used as an independent prognostic marker for tumor recurrence after complete resection of GIST, and the cutoff value of mitotic count that might predict tumor relapse is 4/50 HPF. However, more clinical studies with greater number of cases with fluorescent in situ hybridization integration are recommended.

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