AB007。滋养细胞抗原2 (Trop2)在胸腺上皮肿瘤中的表达

Vincent Yeung, Jacob P Zaemes, Justin Yeh, Cardoza Giancarlo, Jaeil Ahn, J. Reuss, B. Kallakury, Stephen V. Liu, A. Duttargi, G. Khan, Chul Kim
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Of the patients for whom tumor samples were available, immunohistochemistry (IHC) membranous staining for Trop2 was performed using SP295 rabbit IgG anti-human Trop2 (Abcam, Waltham, MA, USA). When available, IHC staining for Trop2 was performed on normal thymus tissue from the same patients. Positivity required at least 10% of the tumor cells to be stained, with an intensity scored of 1+ (weak), 2+ (moderate), and 3+ (strong).3 Medical records of the included patients were reviewed to identify clinical characteristics including age, sex, stage of disease, and WHO subtype. Results Thirty TET samples from 29 patients (17 patients with thymoma and 12 patients with thymic carcinoma) were identified. One patient with thymic carcinoma had two samples from different time points. From the same set of patients, 15 samples of normal thymus tissue were available. In the normal thymus tissue, 10 samples (67%) showed no positivity of Trop2, while the remaining 5 samples (33%) showed only 1+ IHC staining. In the thymoma samples, 4 (24%) showed 0 or 1+ IHC staining, while 13 (76%) showed 2+ or 3+ staining. Of the 12 thymic carcinoma samples, all exhibited Trop2 expression; three samples (23%) showed 1+ IHC staining while 8 (62%) showed 2+ staining and 2 (15%) showed 3+ staining. Conclusions Trop2 is readily expressed in both thymomas and thymic carcinomas with a higher degree of expression in thymic carcinoma. The expression of Trop-2 was lower in normal thymic tissue compared with TETs. 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Results Thirty TET samples from 29 patients (17 patients with thymoma and 12 patients with thymic carcinoma) were identified. One patient with thymic carcinoma had two samples from different time points. From the same set of patients, 15 samples of normal thymus tissue were available. In the normal thymus tissue, 10 samples (67%) showed no positivity of Trop2, while the remaining 5 samples (33%) showed only 1+ IHC staining. In the thymoma samples, 4 (24%) showed 0 or 1+ IHC staining, while 13 (76%) showed 2+ or 3+ staining. Of the 12 thymic carcinoma samples, all exhibited Trop2 expression; three samples (23%) showed 1+ IHC staining while 8 (62%) showed 2+ staining and 2 (15%) showed 3+ staining. Conclusions Trop2 is readily expressed in both thymomas and thymic carcinomas with a higher degree of expression in thymic carcinoma. The expression of Trop-2 was lower in normal thymic tissue compared with TETs. 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引用次数: 0

摘要

滋养细胞抗原2 (Trophoblastic antigen 2, Trop2)是一种细胞表面糖蛋白,在多种类型的癌症中表达,包括乳腺癌、非小细胞肺癌和胃肠道癌1。针对trop2表达肿瘤的治疗干预是一个活跃的研究领域。在胸腺上皮肿瘤(TETs)中,Trop2的表达和Trop2定向治疗(如抗体-药物偶联(ADC))的使用尚未被研究。方法回顾性分析2011-2021年在MedStar乔治城大学医院接受tet治疗的患者。在有肿瘤样本的患者中,使用SP295兔IgG抗人Trop2 (Abcam, Waltham, MA, USA)对Trop2进行免疫组织化学(IHC)膜染色。在可能的情况下,对来自同一患者的正常胸腺组织进行了Trop2的免疫组化染色。阳性要求至少10%的肿瘤细胞染色,强度评分为1+(弱),2+(中等)和3+(强)对纳入患者的医疗记录进行审查,以确定临床特征,包括年龄、性别、疾病分期和WHO亚型。结果29例患者(胸腺瘤17例,胸腺癌12例)共检出TET样本30份。一名胸腺癌患者有两个不同时间点的样本。从同一组患者中,可获得15个正常胸腺组织样本。正常胸腺组织中,有10例(67%)未见Trop2阳性,其余5例(33%)仅见1+ IHC染色。胸腺瘤4例(24%)IHC染色为0 +或1+,13例(76%)IHC染色为2+或3+。12例胸腺癌均表达Trop2;1+ IHC染色3例(23%),2+染色8例(62%),3+染色2例(15%)。结论Trop2在胸腺瘤和胸腺癌中均有表达,在胸腺癌中表达程度更高。与TETs相比,正常胸腺组织中Trop-2的表达较低。Trop-2在TETs中的表达增加表明,Trop-2是一个有吸引力的靶向治疗靶点。
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AB007. Expression of trophoblastic antigen 2 (Trop2) in thymic epithelial tumors
Background Trophoblastic antigen 2 (Trop2) is a cell surface glycoprotein expressed in multiple types of cancers, including breast cancer, non-small cell lung cancer, and gastrointestinal cancers1. Therapeutic intervention targeting Trop2-expressing tumors is an active area of investigation. Trop2 expression and the use of Trop2-directed therapy such as antibody-drug conjugate (ADC) have not yet been investigated in thymic epithelial tumors (TETs). Methods Patients with TETs treated at MedStar Georgetown University Hospital between 2011–2021 were retrospectively identified. Of the patients for whom tumor samples were available, immunohistochemistry (IHC) membranous staining for Trop2 was performed using SP295 rabbit IgG anti-human Trop2 (Abcam, Waltham, MA, USA). When available, IHC staining for Trop2 was performed on normal thymus tissue from the same patients. Positivity required at least 10% of the tumor cells to be stained, with an intensity scored of 1+ (weak), 2+ (moderate), and 3+ (strong).3 Medical records of the included patients were reviewed to identify clinical characteristics including age, sex, stage of disease, and WHO subtype. Results Thirty TET samples from 29 patients (17 patients with thymoma and 12 patients with thymic carcinoma) were identified. One patient with thymic carcinoma had two samples from different time points. From the same set of patients, 15 samples of normal thymus tissue were available. In the normal thymus tissue, 10 samples (67%) showed no positivity of Trop2, while the remaining 5 samples (33%) showed only 1+ IHC staining. In the thymoma samples, 4 (24%) showed 0 or 1+ IHC staining, while 13 (76%) showed 2+ or 3+ staining. Of the 12 thymic carcinoma samples, all exhibited Trop2 expression; three samples (23%) showed 1+ IHC staining while 8 (62%) showed 2+ staining and 2 (15%) showed 3+ staining. Conclusions Trop2 is readily expressed in both thymomas and thymic carcinomas with a higher degree of expression in thymic carcinoma. The expression of Trop-2 was lower in normal thymic tissue compared with TETs. The increased expression of Trop-2 in TETs suggests that Trop2 is an attractive therapeutic target for Trop-2 directed therapy.
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Imaging of thymic epithelial tumors-a clinical practice review. Locally advanced thymic epithelial tumors: a foreword to the special series. Genomic insights into molecular profiling of thymic carcinoma: a narrative review. Re-evaluation and operative indications after induction therapy for thymic epithelial tumors. Narrative review of indication and management of induction therapy for thymic epithelial tumors.
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