Department of Medical Oncology, Shanghai Pulmonary Hospital, Thoracic Cancer Institute, Tongji University School of Medicine, Shanghai, 200433, PR China.
Department of Pathology, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, 200433, PR China.
Clin Lung Cancer. 2018 Jul;19(4):e421-e430. doi: 10.1016/j.cllc.2018.02.008. Epub 2018 Mar 31.
Programmed death-ligand 1 (PD-L1) expression using immunohistochemistry is approved by the US Food and Drug Administration to guide treatment with anti-programmed death-1/PD-L1 monoantibodies. However, intratumoral heterogeneity of PD-L1 expression and the accordance between primary and metastatic lesions remains unresolved.
PD-L1 expression was evaluated in tumor cells and tumor-infiltrating lymphocytes (TILs) of surgically resected lung adenosquamous carcinoma. Discrepancy of PD-L1 expression and cluster of differentiation 8-positive TILs of different histologic components was investigated. PD-L1 expression was also compared between primary tumor and nodal metastases.
The study included a total of 72 lung adenosquamous carcinomas. Fifteen patients (20.8%) and 25 patients (34.7%) were positive for PD-L1 expression in adenomatous and squamous components respectively, with a cutoff value of 5%. We found that 57.8% of cases showed consistent PD-L1 expression in tumor cells in the different histological components at a cutoff of 1%, and 48.1% of cases were likewise consistent at a cutoff of 5%. In paired squamous components of metastatic nodes and primary lesions, 90% and 80% of cases of PD-L1 expression were consistent, at cutoffs of 1% and 5%, respectively. For the adenomatous component of tumor/metastasis pairs, 77.8% of cases at the 1% cutoff and 74.1% of cases at the 5% cutoff were consistent, partially attributed to the difference of predominant histologic patterns.
PD-L1 expression showed discrepancy in different histological components within a tumor and consistency in paired histological type between tumor and metastases. Different pathological features might contribute to the heterogeneous PD-L1 expression in patients with non-small-cell lung cancer.
程序性死亡配体 1(PD-L1)的免疫组织化学表达已被美国食品和药物管理局批准用于指导抗程序性死亡-1/PD-L1 单克隆抗体的治疗。然而,肿瘤内 PD-L1 表达的异质性以及原发性和转移性病变之间的一致性仍未得到解决。
评估了手术切除的肺腺鳞癌中肿瘤细胞和肿瘤浸润淋巴细胞(TIL)的 PD-L1 表达。研究了不同组织学成分的 PD-L1 表达差异和 CD8 阳性 TIL 簇。还比较了原发性肿瘤和淋巴结转移之间的 PD-L1 表达。
本研究共纳入 72 例肺腺鳞癌。15 例(20.8%)和 25 例(34.7%)患者在腺性和鳞状成分中 PD-L1 表达阳性,截断值为 5%。我们发现,在不同组织学成分中,以 1%为截断值时,57.8%的病例肿瘤细胞中 PD-L1 表达一致,以 5%为截断值时,48.1%的病例一致。在配对的转移性淋巴结和原发性病变的鳞状成分中,以 1%和 5%为截断值时,PD-L1 表达的一致性分别为 90%和 80%。对于肿瘤/转移对的腺性成分,以 1%为截断值时,77.8%的病例一致,以 5%为截断值时,74.1%的病例一致,部分原因是主要组织学模式的差异。
肿瘤内不同组织学成分的 PD-L1 表达存在差异,肿瘤与转移之间配对组织学类型的表达一致。不同的病理特征可能导致非小细胞肺癌患者 PD-L1 表达的异质性。