PD-L1在甲状腺髓样癌中的表达及其与临床病理的关系。

IF 1.1 Q4 PATHOLOGY
Yasemin Kemal, Sultan Çalişkan, Seda Gun, Mehmet Kefeli
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引用次数: 2

摘要

目的:< /strong >甲状腺髓样癌(MTC)是一种起源于滤泡旁C细胞的罕见肿瘤。它比分化型甲状腺癌具有更强的侵袭性生物学行为,并且对放射性碘治疗不敏感。Vandetanib和cabozantinib是新批准的晚期酪氨酸激酶抑制剂,但新的有效的全身治疗可能是至关重要的,并且需要对这些患者的临床管理。我们的目的是评估程序性死亡配体1 (PD-L1)的表达,这是一个新的免疫治疗靶点,在我们的MTC队列中,确定它是否与临床和病理特征有关。< strong >材料与方法:< /strong >本回顾性研究纳入41例MTC,中位随访54个月。免疫组织化学方法检测PD-L1单克隆抗体(SP263克隆)。超过1%的肿瘤细胞呈完全和/或部分膜性染色模式为阳性。分析PD-L1表达与临床病理及预后的相关性。结果:41例肿瘤中有5例(12.2%)PD-L1阳性。所有肿瘤的PD-L1染色程度均较低(< 5%)。在我们的MTC患者中,PD-L1表达没有临床病理和预后相关性。结论:< /strong >尽管PD-L1表达可能是预测各种癌症预后和对检查点抑制剂反应的潜在生物标志物,但在我们的病例中,我们未发现PD-L1表达与临床病理特征之间有任何显著相关性。患者数量较多的研究仍需要进行更全面的分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

PD-L1 Expression in Medullary Thyroid Carcinoma and Its Association with Clinicopathological Findings.

PD-L1 Expression in Medullary Thyroid Carcinoma and Its Association with Clinicopathological Findings.

PD-L1 Expression in Medullary Thyroid Carcinoma and Its Association with Clinicopathological Findings.

< strong > Objective: < /strong > Medullary thyroid carcinoma (MTC) is a rare tumor originating from parafollicular C cells. It has more aggressive biologic behavior than differentiated thyroid carcinomas, and it is insensitive to treatment with radioactive iodine. Vandetanib and cabozantinib are the newly approved tyrosine kinase inhibitors in advanced stages, but novel effective systemic therapeutics could be crucial and needed for the clinical management of these patients. We aimed to evaluate the Programmed death-ligand 1 (PD-L1) expression, which is a novel immunotherapy target, in our MTC cohort, and determine whether it has an association with clinical and pathological features. < strong > Material and Method: < /strong > This retrospective study involved 41 cases of MTC with a median follow-up of 54 months. PD-L1 monoclonal antibody (SP263 clone) was investigated immunohistochemically. Complete and/or partial membranous staining pattern in more than 1% of tumor cells was considered positive. The correlations of PD-L1 expression with clinicopathologic and prognostic features were analyzed. < strong > Results: < /strong > PD-L1 positivity was detected in 5 (12.2%) of 41 tumors. The extent of PD-L1 staining was low ( < 5%) for all tumors. There was no clinicopathologic and prognostic relevance regarding PD-L1 expression in our MTC patients. < strong > Conclusion: < /strong > Although PD-L1 expression could be a potential biomarker to predict the prognosis of various cancers and response to checkpoint inhibitors, we did not find any significant correlation between PD-L1 expression and clinicopathologic features in our cases. Studies with larger patient numbers are still required to perform a more comprehensive analysis.

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来源期刊
CiteScore
1.90
自引率
10.00%
发文量
23
审稿时长
14 weeks
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