Department of Medical Oncology, Istinye University, Faculty of Medicine, İSTANBUL, TURKEY.
Turk Patoloji Derg. 2022;38(2):106-113. doi: 10.5146/tjpath.2021.01558.
< 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.
甲状腺髓样癌(MTC)是一种起源于滤泡旁 C 细胞的罕见肿瘤。与分化型甲状腺癌相比,其生物学行为更为侵袭性,且对放射性碘治疗不敏感。凡德他尼和卡博替尼是晚期新批准的酪氨酸激酶抑制剂,但对于这些患者的临床管理,新型有效的全身治疗可能是至关重要和必要的。我们旨在评估我们的 MTC 队列中程序性死亡配体 1(PD-L1)的表达,这是一种新的免疫治疗靶点,并确定其与临床和病理特征是否存在关联。
本回顾性研究纳入了 41 例 MTC 病例,中位随访时间为 54 个月。采用 PD-L1 单克隆抗体(SP263 克隆)进行免疫组织化学检测。肿瘤细胞中超过 1%的完全或部分膜染色模式被认为是阳性的。分析 PD-L1 表达与临床病理和预后特征的相关性。
41 例肿瘤中有 5 例(12.2%)检测到 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 表达与临床病理特征之间没有明显的相关性。
虽然 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,但我们在我们的病例中没有发现 PD-L1 表达与临床病理特征之间存在任何显著相关性。仍需要进行更多的研究来进行更全面的分析。