Pathology Laboratory, Çankırı State Hospital, Çankırı, Turkey
Department of Pathology, İstanbul University-Cerrahpaşa, Cerrahpaşa School of Medicine, İstanbul, Turkey
Balkan Med J. 2019 May 10;36(3):184-189. doi: 10.4274/balkanmedj.galenos.2018.2018.0392. Epub 2018 Dec 28.
Prognostic significance of the programmed death-ligand-1 status in non-small cell lung carcinoma remains controversial.
To show the programmed death-ligand-1 expression status in patients with non-small cell lung carcinoma and its effect on the prognosis and the relationship with clinicopathologic data.
Retrospective cross-sectional study.
The study included 208 cases who were diagnosed with NSCLC and who underwent surgical resection between 2001 and 2012. Programmed death-ligand-1 (SP142 clone) was applied to the histological sections acquired from the microarray paraffin blocks with immunohistochemistry. Staining intensity was scored as weak (+, 1), moderate (++, 2), and strong (+++, 3). Percentage (0%-100%) was multiplied by staining intensity (1-2-3) to calculate the H score. Four different cut-off values were used; 1: ≥1% (independent of intensity), 2: ≥5% (independent of intensity), 3: ≥5% moderate/strong staining (except for weak staining), 4: H score ≥30 values were considered positive. In this study, staining a single cell at any intensity was considered positive.
Thirty-four out 208 cases (16.3%) had PDL-1 positive staining. PDL-1 expression was observed in patients with non-small cell lung carcinoma independent of the histological type or subtype (range; 0-25%). When the cut-off level was set to ≥5% with moderate and strong staining, the median overall survival was 45 months for the PD-L1 positive group and not reached for the PD-L1 negative group (p-value 0.024). PD-L1 positivity was significantly higher in patients over the age of 60 years and in cases with a tumor diameter of more than 5 cm (p=0.023 and 0.025, respectively).
PD-L1 expression is positive in 16.3% of patients with non-small cell lung cancer and may have a negative prognostic value.
程序性死亡配体-1(PD-L1)状态在非小细胞肺癌(NSCLC)中的预后意义仍存在争议。
展示 NSCLC 患者的 PD-L1 表达状态及其对预后的影响,并探讨其与临床病理数据的关系。
回顾性病例对照研究。
纳入 208 例于 2001 年至 2012 年间接受手术切除的 NSCLC 患者。采用免疫组化法,应用 SP142 克隆检测组织微阵列石蜡块中的 PD-L1。染色强度评分:弱(+,1)、中(++,2)、强(+++,3)。将阳性百分比(0%-100%)乘以染色强度(1-2-3),计算 H 评分。本研究共采用了 4 种不同的截断值:1:≥1%(不论强度);2:≥5%(不论强度);3:≥5%中/强染色(除弱染色外);4:H 评分≥30 视为阳性。本研究中,任何强度的单个细胞染色阳性即视为阳性。
208 例患者中,34 例(16.3%)PD-L1 染色阳性。PD-L1 表达与 NSCLC 的组织学类型或亚型无关(范围:0-25%)。当截断值设定为≥5%的中/强染色时,PD-L1 阳性组的中位总生存期为 45 个月,而 PD-L1 阴性组未达到(p 值=0.024)。PD-L1 阳性患者的年龄大于 60 岁和肿瘤直径大于 5cm 的比例显著更高(p=0.023 和 0.025)。
PD-L1 表达在 16.3%的 NSCLC 患者中呈阳性,可能具有负预后价值。