Personalized Medicine Laboratory, Instituto Nacional de Cancerología (INCan), Mexico City, 14080, Mexico.
Pathology department, Instituto Nacional de Cancerología (INCan), Mexico City, 14080, Mexico.
J Transl Med. 2024 Sep 12;22(1):841. doi: 10.1186/s12967-024-05471-6.
CD155 is a transmembrane protein that inhibits antitumor immune response and represents a predictor of worse prognosis in non-small-cell lung cancer (NSCLC). However, it remains unexplored its association with clinical characteristics and genomic status of Latin American patients. This study characterizes the CD155 expression and its clinical implications in this population.
Tissue biopsies from 86 patients with locally-advanced or metastatic NSCLC were assessed for CD155 protein expression, ALK rearrangements and EGFR mutations. Cutoff values for high CD155 expression (CD155) were determined from receiver operating characteristic (ROC) curves according to 2-year survival. It was evaluated its association with clinicopathological features, median progression-free survival (mPFS) and overall survival (mOS).
the cutoff score for CD155 was 155 in the entire cohort and in patients without oncogenic alterations, and it was 110 in patients with oncogenic alterations. Eighty-four patients (97.7%) were CD155 positive, of which fifty-six (65.0%) had CD155. EGFR L858R mutation related to lower CD155 IHC score than exon 19 deletion. Individuals with CD155 showed a shorter mOS (13.0 vs. 30.8 months; HR: 1.96 [95% CI, 1.15-3.35]; p = 0.014). Patients without oncogenic alterations having a CD155 displayed shorter mPFS (1.6 vs. 6.4 months, HR: 2.09 [95% CI, 1.06-4.20]; p = 0.034) and mOS (2.9 vs. 23.1 months; HR: 1.27 [95% CI, 1.07- 4.42]; p = 0.032). Patients with oncogenic alterations having CD155 only showed a trend to shorter mOS (26.3 vs. 52.0 months; HR: 2.39 [95% CI, 0.98-5.83]; p = 0.058).
CD155 is a predictor of worse outcomes in patients with advanced NSCLC, predominantly among those without oncogenic alterations. CD155 could be a potential biomarker and a molecular target in patients with poor responses to current therapies.
CD155 是一种跨膜蛋白,可抑制抗肿瘤免疫反应,是预测非小细胞肺癌(NSCLC)预后不良的指标。然而,其与拉丁美洲患者的临床特征和基因组状态的关系仍不清楚。本研究旨在描述 CD155 在该人群中的表达及其临床意义。
对 86 例局部晚期或转移性 NSCLC 患者的组织活检标本进行 CD155 蛋白表达、ALK 重排和 EGFR 突变检测。根据 2 年生存率,通过受试者工作特征(ROC)曲线确定高 CD155 表达(CD155)的截断值。评估其与临床病理特征、中位无进展生存期(mPFS)和总生存期(mOS)的关系。
整个队列和无致癌改变患者的 CD155 截断值为 155,有致癌改变患者的截断值为 110。84 例患者(97.7%)CD155 阳性,其中 56 例(65.0%)CD155 高表达。EGFR L858R 突变与外显子 19 缺失相比,CD155 IHC 评分较低。CD155 阳性患者的 mOS 较短(13.0 与 30.8 个月;HR:1.96 [95%CI,1.15-3.35];p=0.014)。无致癌改变且 CD155 阳性患者的 mPFS 较短(1.6 与 6.4 个月,HR:2.09 [95%CI,1.06-4.20];p=0.034)和 mOS 较短(2.9 与 23.1 个月;HR:1.27 [95%CI,1.07-4.42];p=0.032)。有致癌改变且 CD155 阳性患者的 mOS 虽有缩短趋势(26.3 与 52.0 个月;HR:2.39 [95%CI,0.98-5.83];p=0.058)。
CD155 是晚期 NSCLC 患者预后不良的预测指标,主要见于无致癌改变的患者。CD155 可能是对当前治疗反应不佳的患者的潜在生物标志物和分子靶点。