Department of General Thoracic Surgery, National Hospital Organization Kinki-Chuo Chest Medical Center, Sakai, Japan.
Department of Laboratory Medicine and Pathology, National Hospital Organization Kinki-Chuo Chest Medical Center, Sakai, Japan.
Jpn J Clin Oncol. 2022 Mar 3;52(3):281-285. doi: 10.1093/jjco/hyab202.
The association between non-small cell lung cancer histology and programmed death-ligand 1 expression remains controversial. We retrospectively analyzed histological dependence of the programmed death-ligand 1 expression by a multiple regression analysis of 356 non-small cell lung cancer patients. The programmed death-ligand 1 expression patterns of adenocarcinoma were consistent with a pathological predominant growth pattern as a reference to papillary adenocarcinoma: minimally invasive adenocarcinoma[partial regression coefficient (B), 0.17; 95% confidence interval, 0.05-0.59], lepidic adenocarcinoma (B, 0.46; 95% confidence interval, 0.23-0.90), acinar adenocarcinoma (B, 1.98; 95% confidence interval, 1.05-3.76) and solid adenocarcinoma (B, 5.11; 95% confidence interval, 2.20-11.9). In histology other than adenocarcinoma, the programmed death-ligand 1 expression tended to be high with poor differentiation: adenosquamous carcinoma (B, 4.17; 95% confidence interval, 1.05-16.6), squamous cell carcinoma (B, 4.32; 95% confidence interval, 2.45-7.62) and pleomorphic carcinoma (B, 13.0; 95% confidence interval, 4.43-38.2). We showed quantitatively that the programmed death-ligand 1 expression in non-small cell lung cancer tended to be clearly histology-dependent, with more poorly differentiated histology showing a higher expression.
非小细胞肺癌组织学与程序性死亡配体 1 表达之间的关系仍存在争议。我们通过对 356 例非小细胞肺癌患者的多元回归分析,回顾性分析了程序性死亡配体 1 表达的组织学依赖性。腺癌的程序性死亡配体 1 表达模式与以乳头状腺癌为主的病理生长模式一致:微浸润性腺癌[偏回归系数(B),0.17;95%置信区间,0.05-0.59]、贴壁性腺癌(B,0.46;95%置信区间,0.23-0.90)、腺泡性腺癌(B,1.98;95%置信区间,1.05-3.76)和实体性腺癌(B,5.11;95%置信区间,2.20-11.9)。在非腺癌组织学中,分化较差的程序性死亡配体 1 表达倾向于升高:腺鳞癌(B,4.17;95%置信区间,1.05-16.6)、鳞状细胞癌(B,4.32;95%置信区间,2.45-7.62)和多形性癌(B,13.0;95%置信区间,4.43-38.2)。我们定量地表明,非小细胞肺癌中程序性死亡配体 1 的表达倾向于明显依赖于组织学,分化越差表达越高。