Takeda Maiko, Kasai Takahiko, Naito Maiko, Tamiya Akihiro, Taniguchi Yoshihiko, Saijo Nobuhiko, Naoki Yoko, Okishio Kyoichi, Shimizu Shigeki, Kojima Kensuke, Nagoya Akihiro, Sakamoto Tetsuki, Utsumi Tomoki, Yoon Hyung-Eun, Matsumura Akihide, Atagi Shinji
Department of Laboratory Medicine and Pathology, National Hospital Organization Kinki-Chuo Chest Medical Center, Sakai, Japan.
Department of Internal Medicine, National Hospital Organization Kinki-Chuo Chest Medical Center, Sakai, Japan.
Clin Med Insights Oncol. 2019 Jan 9;13:1179554918821314. doi: 10.1177/1179554918821314. eCollection 2019.
In recent years, the anti-programmed cell death 1 (PD-1) drug pembrolizumab (Keytruda) was approved for treatment of unresectable advanced non-small cell lung cancer (NSCLC) as first- or second-line therapy depending on the clone 22C3-programmed death-ligand 1 (PD-L1) immunohistochemical expression score by the companion diagnostic assay. We herein evaluated 22C3-PD-L1 expression of NSCLC in a single institution experience and compared it with clinicopathologic features.
We assessed 22C3-PD-L1 expressions of 411 patients with NSCLC from our institution, including in past specimens. Programmed death-ligand 1 immunohistochemistry (IHC) testing was performed using the PD-L1 clone 22C3 pharmDx kit (Agilent Technologies/Dako, Carpinteria, CA, USA). Patients were separated into 3 groups with <1% (no expression), 1% to 49% (low expression), or ⩾50% (high expression) positive tumor cells.
In all, 137 patients (33%) did not express PD-L1, 155 (38%) showed low expression, and 119 (29%) demonstrated high expression. Archival samples showed lower PD-L1 expression than that of recent samples, and the ratios of no expression case significantly increased by using paraffin blocks embedded particularly in more than 4 years ago. Programmed death-ligand 1 positivity was significantly associated with male sex, smoking, higher tumor grade, squamous cell carcinoma in histologic type, wild-type , and rearrangement positive.
The rate of 22C3-PD-L1 expression of NSCLC detected in this study was similar to the frequencies of the previous reports, although the ratio of expression case decreased when using old paraffin blocks.
近年来,抗程序性细胞死亡蛋白1(PD-1)药物帕博利珠单抗(可瑞达)被批准用于治疗不可切除的晚期非小细胞肺癌(NSCLC),根据伴随诊断检测的克隆22C3程序性死亡配体1(PD-L1)免疫组化表达评分作为一线或二线治疗。我们在此评估了单一机构经验中NSCLC的22C3-PD-L1表达,并将其与临床病理特征进行比较。
我们评估了本机构411例NSCLC患者的22C3-PD-L1表达,包括既往标本。使用PD-L1克隆22C3免疫组化检测试剂盒(安捷伦科技/达科,美国加利福尼亚州卡平特里亚)进行程序性死亡配体1免疫组化(IHC)检测。患者被分为3组,阳性肿瘤细胞<1%(无表达)、1%至49%(低表达)或⩾50%(高表达)。
总共137例患者(33%)未表达PD-L1,155例(38%)显示低表达,119例(29%)显示高表达。存档样本显示PD-L1表达低于近期样本,特别是使用4年以上包埋的石蜡块时无表达病例的比例显著增加。程序性死亡配体1阳性与男性、吸烟、更高的肿瘤分级、组织学类型为鳞状细胞癌、野生型以及重排阳性显著相关。
本研究中检测到的NSCLC的22C3-PD-L1表达率与先前报道的频率相似,尽管使用旧石蜡块时表达病例的比例有所下降。