Programmed Death Ligand 1 (PD-L1) Expression and its Association with Clinicopathologic Profile in Patients with Non-Small Cell Lung Cancer in a Philippine Tertiary Medical Center

Flora Mae Sta. Ines, J. Andal, R. M. Santiago, S. Sandoval, D. Ang
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Abstract

Introduction. The current management of advanced non-small cell lung cancer (NSCLC) includes the characterization of Programmed Death Ligand-1 (PD-L1) expression for potential immune checkpoint inhibitor treatment. There is currently no available data regarding the patterns of PD-L1 expression in NSCLC, as well as their association with clinicopathologic profile in Filipino patients. Methodology. Clinicopathologic characteristics of 187 consecutive NSCLC clinical samples with PD-L1 testing using the clone 22C3 pharmaDx kit were collected. The presence of stromal tumor-infiltrating lymphocytes (TILs) were assessed in hematoxylin and eosin-stained slides. PD-L1 expression on tumor cells (TC) and stromal TILs were evaluated. Results. Of the 187 cases, there were 112 males and 75 females. The mean age at diagnosis was 66.4 years old (32-92 years old). It is composed of 131 cases of Adenocarcinoma, 15 Squamous cell carcinoma, 4 Adenosquamous carcinoma, 32 Non-small cell carcinoma, not otherwise specified, 3 poorly differentiated malignancy, 1 Large cell carcinoma, and 1 Mucinous carcinoma. Specimen types included 17 pleural fluid cell blocks, 60 tumor cell block samples, and 110 tissue biopsies. Tumor cell PD-L1 expression was identified in 59.1% of the 110 tissue biopsies. PD-L1 TPS for histologic specimens are as follows: TPS >50%, TPS 1-49%, and TPS <1% were observed in 23.6%, 35.5%, and 40.9% in our lung cancer cohort, respectively. Of the 77 cytology specimens, 50.6% presented with TC PD-L1 expression. TPS for this subgroup include: 49.4% with no PD-L1 expression, 35.1% with low PD-L1 expression, and 15.6% showing high PD-L1 expression. PD-L1 expression on TC did not correlate with age, sex, or histology for both specimen type subgroups. Stromal tumor-infiltrating lymphocytes were noted in 74.5% of tissue biopsies. Tumor cell block samples did not demonstrate stromal TILs. For tissue biopsies, female gender and TPS 1-49% were more likely to have <50% PD-L1 expression on TILs. Conclusion. Overall TC PD-L1 expression was observed in more than half (55.6%) of NSCLC patients in our cohort. The prognostic value of PD-L1 and clinical response to immune checkpoint inhibitors in the Filipino population needs to be further investigated.
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程序性死亡配体1 (PD-L1)表达及其与菲律宾三级医疗中心非小细胞肺癌患者临床病理特征的关系
介绍。目前晚期非小细胞肺癌(NSCLC)的治疗包括程序性死亡配体-1 (PD-L1)表达的表征,以用于潜在的免疫检查点抑制剂治疗。目前还没有关于菲律宾NSCLC患者PD-L1表达模式及其与临床病理特征的关系的可用数据。方法。使用克隆22C3 pharmaDx试剂盒收集187例连续进行PD-L1检测的NSCLC临床样本的临床病理特征。在苏木精和伊红染色的玻片中评估基质肿瘤浸润淋巴细胞(TILs)的存在。检测PD-L1在肿瘤细胞(TC)和间质til中的表达。结果。在187宗个案中,男性112宗,女性75宗。平均诊断年龄为66.4岁(32-92岁)。其中腺癌131例,鳞状细胞癌15例,腺鳞癌4例,非小细胞癌32例,未另行说明,低分化恶性3例,大细胞癌1例,粘液癌1例。标本类型包括17例胸腔积液细胞块、60例肿瘤细胞块和110例组织活检。110例组织活检中有59.1%的肿瘤细胞PD-L1表达。组织学标本PD-L1 TPS情况如下:在我们的肺癌队列中,TPS >50%、TPS 1-49%和TPS <1%分别为23.6%、35.5%和40.9%。77例细胞学标本中,50.6%呈现TC PD-L1表达。该亚组TPS包括:无PD-L1表达49.4%,低PD-L1表达35.1%,高PD-L1表达15.6%。在两个标本类型亚组中,TC上PD-L1的表达与年龄、性别或组织学无关。74.5%的组织活检发现基质肿瘤浸润淋巴细胞。肿瘤细胞块样本未显示间质TILs。在组织活检中,女性和TPS 1-49%的患者在til上PD-L1表达<50%的可能性更大。结论。在我们的队列中,超过一半(55.6%)的NSCLC患者中观察到总TC PD-L1表达。菲律宾人群中PD-L1的预后价值和对免疫检查点抑制剂的临床反应需要进一步研究。
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