Transcription Factor Immunohistochemistry in the Classification of Pituitary Neuroendocrine Tumor/Adenoma: Proposal in a Limited-Resource Setting.

IF 3.7 3区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY Archives of pathology & laboratory medicine Pub Date : 2024-02-01 DOI:10.5858/arpa.2021-0479-OA
Ridhi Sood, Debajyoti Chatterjee, Pinaki Dutta, Bishan Dass Radotra
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Abstract

Context.—: Pituitary neuroendocrine tumors/adenomas are common intracranial tumors that require accurate subtyping because each tumor differs in its biologic behavior and response to treatment. Pituitary-specific transcription factors allow for improved lineage identification and diagnosis of newly introduced variants.

Objective.—: To assess the usefulness of transcription factors and design a limited panel of immunostains for classification of pituitary neuroendocrine tumors/adenoma.

Design.—: A total of 356 tumors were classified as per expression of pituitary hormones and transcription factors T-box family member TBX19 (TPIT), pituitary-specific POU-class homeodomain (PIT1), and steroidogenic factor-1 (SF-1). The resultant classification was correlated with patients' clinical and biochemical features. The performance and relevance of individual immunostains were analyzed.

Results.—: Reclassification of 34.8% (124 of 356) of pituitary neuroendocrine tumors/adenoma was done after application of transcription factors. The highest agreement with final diagnosis was seen using a combination of hormone and transcription factors. SF-1 had higher sensitivity, specificity, and predictive value compared with follicle-stimulating hormone and luteinizing hormone. On the other hand, TPIT and PIT1 had similar performance and Allred scores compared with their respective hormones.

Conclusions.—: SF-1 and PIT1 should be included in the routine panel for guiding the classification. PIT1 positivity needs to be followed by hormone immunohistochemistry, especially in nonfunctional cases. TPIT and adrenocorticotropin can be used interchangeably as per availability of the lab.

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转录因子免疫组化在垂体神经内分泌肿瘤/腺瘤分类中的应用:在资源有限情况下的建议。
背景:垂体神经内分泌肿瘤/腺瘤是常见的颅内肿瘤,由于每种肿瘤的生物行为和对治疗的反应各不相同,因此需要进行准确的亚型鉴定。脑垂体特异性转录因子可改善对新引入变体的系谱鉴定和诊断:评估转录因子的作用,并设计一个有限的免疫印迹小组,用于垂体神经内分泌肿瘤/腺瘤的分类:根据垂体激素和转录因子T-box家族成员TBX19(TPIT)、垂体特异性POU-class homeodomain(PIT1)和类固醇生成因子-1(SF-1)的表达情况,对356例肿瘤进行分类。由此得出的分类结果与患者的临床和生化特征相关。对各个免疫标记的性能和相关性进行了分析:应用转录因子后,34.8%(356 例中的 124 例)垂体神经内分泌肿瘤/腺瘤得到了重新分类。结合使用激素和转录因子与最终诊断的一致性最高。与卵泡刺激素和促黄体生成素相比,SF-1 具有更高的敏感性、特异性和预测价值。另一方面,TPIT 和 PIT1 与各自的激素相比,具有相似的性能和 Allred 评分:结论:SF-1 和 PIT1 应被纳入常规检查项目,用于指导分类。PIT1 阳性后需要进行激素免疫组化,尤其是在无功能病例中。TPIT和促肾上腺皮质激素可根据实验室条件交替使用。
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来源期刊
CiteScore
9.20
自引率
2.20%
发文量
369
审稿时长
3-8 weeks
期刊介绍: Welcome to the website of the Archives of Pathology & Laboratory Medicine (APLM). This monthly, peer-reviewed journal of the College of American Pathologists offers global reach and highest measured readership among pathology journals. Published since 1926, ARCHIVES was voted in 2009 the only pathology journal among the top 100 most influential journals of the past 100 years by the BioMedical and Life Sciences Division of the Special Libraries Association. Online access to the full-text and PDF files of APLM articles is free.
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