Programmed death-1 ligand 1 and 2 are highly expressed in pleomorphic carcinomas of the lung: Comparison of sarcomatous and carcinomatous areas

被引:153
作者
Kim, Sehui [1 ,2 ]
Kim, Moon-Young [1 ]
Koh, Jaemoon [1 ,2 ]
Go, Heounjeong [3 ]
Lee, Dong Soo [4 ,5 ]
Jeon, Yoon Kyung [1 ,2 ]
Chung, Doo Hyun [1 ,2 ,6 ]
机构
[1] Seoul Natl Univ Hosp, Dept Pathol, Seoul 110744, South Korea
[2] Seoul Natl Univ, Coll Med, Dept Pathol, Seoul 151, South Korea
[3] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Pathol, Seoul, South Korea
[4] Seoul Natl Univ, Coll Med, Seoul Natl Univ Hosp, Dept Nucl Med, Seoul, South Korea
[5] Seoul Natl Univ, Coll Med, Dept Mol Med & Biopharmaceut Sci, Seoul, South Korea
[6] Seoul Natl Univ, Coll Med, Dept Biomed Sci, Seoul, South Korea
关键词
Programmed death-1; Programmed death-1 ligand 1; Pleomorphic carcinoma of the lung; Sarcomatoid carcinoma of the lung; Cancer immunotherapy; MESENCHYMAL TRANSITION; CELL CARCINOMA; CANCER-CELLS; T-CELLS; PD-L1; IMMUNOSUPPRESSION; METASTASIS; ANTIBODY; SAFETY; EMT;
D O I
10.1016/j.ejca.2015.08.013
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Pleomorphic carcinoma (PC) of the lung is a rare type of poorly differentiated non-small cell lung carcinoma (NSCLC) that belongs to sarcomatoid carcinoma (SC). It exhibits aggressive behaviour and resistance to chemotherapy and radiotherapy. Recently, immunotherapy targeting the programmed death-1 (PD-1)/PD ligand 1 (PD-L1) pathway has demonstrated favourable clinical outcomes in NSCLC. However, the expression patterns of PD-1-related molecules in pulmonary PC remain elusive. PD-L1 and PD-L2 expression was estimated in 41 cases of PC using immunohistochemistry. CD8(+) and PD-1(+) tumour-infiltrating lymphocytes (TILs) were also evaluated. PD-L1 and PD-L2 were highly expressed in pulmonary PCs (90.2% [37/41)]; 87.8% [36/41]). The amount of CD8(+) or PD-1(+) TILs and the ratio of PD-1(+)/CD8(+) TILs in PC were higher in males, smokers and older patients. PD-L1-positive PCs were infiltrated by higher numbers of CD8(+) TILs compared to PD-L1-negative cases (P = 0.006). Of note, PD-L1 expression in pulmonary PCs was significantly higher in sarcomatous areas than in the carcinomatous portion (P = 0.006). PC patients with a high ratio of PD-1(+)/CD8(+) TILs showed a shorter progression-free survival (P = 0.036), whereas PD-L1 and PD-L2 expression had no prognostic implications. Our study demonstrates that pulmonary PCs very frequently express PD-L1 and PD-L2. Moreover, their expression is higher in sarcomatous cells than in carcinomatous areas. Thus, targeting the PD-1/PD-L1 pathway may represent a potential therapeutic candidate for this aggressive tumour. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2698 / 2707
页数:10
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