Wakuda Kazushige, Morita Meiko, Sekikawa Motoki, Morikawa Noboru, Miura Keita, Doshita Kosei, Iida Yuko, Kodama Hiroaki, Mamesaya Nobuaki, Kobayashi Haruki, Ko Ryo, Ono Akira, Kenmotsu Hirotsugu, Naito Tateaki, Murakami Haruyasu, Muramatsu Koji, Kawata Takuya, Mori Keita, Shimizu Tetsuo, Gon Yasuhiro, Takahashi Toshiaki
Division of Thoracic Oncology, Shizuoka Cancer Center Hospital, 1007 Shimonagakubo, Nagaizumi-cho, Suntou-gun, Shizuoka, 411-8777, Japan.
Division of Pathology, Shizuoka Cancer Center Hospital, 1007 Shimonagakubo, Nagaizumi-cho, Suntou-gun, Shizuoka, 411-8777, Japan.
Int J Clin Oncol. 2024 Feb;29(2):96-102. doi: 10.1007/s10147-023-02451-6. Epub 2024 Jan 6.
Although various companion diagnostic tests of ALK fusion gene-rearrangement are approved, few reports have assessed the concordance of ALK fusion gene-rearrangement in two companion diagnostic tests: next-generation sequencing (NGS) testing and immunohistochemistry (IHC).
The samples evaluated for gene alterations using NGS testing between May 2019 and November 2021 were included in this study. The inclusion criteria were as follows: samples were diagnosed with non-small cell lung cancer; the results of the NGS analysis were informative; and samples had residual specimens for IHC. We performed IHC on the residual specimens and retrospectively collected sample characteristics from medical records.
A total of 185 samples were analyzed using NGS. Twenty-six samples were excluded because of failure to analyze gene alterations using NGS, no residual samples, and inadequate IHC. We analyzed 159 samples. The major histological type was adenocarcinoma (115 samples). The number of surgical and transbronchial lung biopsy specimens was 59 and 56, respectively. ALK fusion gene-rearrangement was detected in four samples using NGS, and five were detected using IHC. The sensitivity and specificity of IHC referred to by NGS were 75.0% and 98.7%, respectively. The concordance rate between IHC and NGS was 98.1%. ALK rearrangement was detected in two patients using IHC but not using NGS. In addition, ALK rearrangement was detected in one patient using NGS but not using IHC.
Our results suggest that IHC and NGS might be complementary tests. In patients suspected of harboring ALK fusion gene-rearrangement, it should be analyzed using another diagnostic method.
尽管多种间变性淋巴瘤激酶(ALK)融合基因重排的伴随诊断检测已获批准,但很少有报告评估两种伴随诊断检测(下一代测序[NGS]检测和免疫组织化学[IHC])中ALK融合基因重排的一致性。
本研究纳入了2019年5月至2021年11月期间使用NGS检测评估基因改变的样本。纳入标准如下:样本被诊断为非小细胞肺癌;NGS分析结果具有信息性;样本有用于IHC的残留标本。我们对残留标本进行了IHC检测,并从病历中回顾性收集了样本特征。
共对185个样本进行了NGS分析。26个样本因无法使用NGS分析基因改变、无残留样本以及IHC不充分而被排除。我们分析了159个样本。主要组织学类型为腺癌(115个样本)。手术和经支气管肺活检标本的数量分别为59个和56个。使用NGS在4个样本中检测到ALK融合基因重排,使用IHC在5个样本中检测到。以NGS为参照,IHC的敏感性和特异性分别为75.0%和98.7%。IHC与NGS之间的一致性率为98.1%。使用IHC在2例患者中检测到ALK重排,但使用NGS未检测到。此外,使用NGS在1例患者中检测到ALK重排,但使用IHC未检测到。
我们的结果表明,IHC和NGS可能是互补检测。对于怀疑存在ALK融合基因重排的患者,应使用另一种诊断方法进行分析。