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肿瘤未知原发灶中程序性死亡配体 1 的表达

Programmed death-ligand 1 expression in carcinoma of unknown primary.

机构信息

Department of Pathology, Yonsei University College of Medicine, Seoul, South Korea.

出版信息

BMC Cancer. 2024 Jun 6;24(1):689. doi: 10.1186/s12885-024-12437-w.

DOI:10.1186/s12885-024-12437-w
PMID:38844907
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11155179/
Abstract

We examined the expression of programmed death-ligand 1 (PD-L1) in carcinoma of unknown primary (CUP) and its potential implications. Tissue microarrays were constructed for 72 CUP cases (histologic subtypes: 22 adenocarcinoma, 15 poorly differentiated carcinoma, 19 squamous cell carcinoma, and 14 undifferentiated carcinoma; clinical subtype: favorable type 17 [23.6%], unfavorable type 55 [76.4%]), with immunohistochemical staining performed for PD-L1 (22C3, SP142, SP263, and 28 - 8), CK7, and CK20 to determine the association between staining results and clinicopathological parameters. In CUP, the PD-L1 positivity rate was 5.6-48.6% (tumor cells [TC] or tumor proportion score [TPS]: 5.6-36.1%, immune cell score [IC]: 8.3-48.6%, combined positive score [CPS]: 16.7%) using different cutoff values for 22C3 (TPS ≥ 1%, CPS ≥ 10), SP142 (TC ≥ 50%, IC ≥ 10%), SP263, and 28 - 8 (TC and IC ≥ 1%). PD-L1 SP142 TC and PD-L1 SP263 IC showed the lowest (5.6%) and highest (48.6%) positivity rates, respectively. The PD-L1 positivity rate did not significantly differ based on the histologic subtype, clinical subtype, or CK7/CK20 across clones. Considering TC κ ≥ 1%, TC κ ≥ 50%, IC κ ≥ 1%, and IC κ ≥ 10%, the PD-L1 positivity rate was TC = 4.2-36.1% and IC = 9.7-48.6%; the overall agreement between antibodies ranged from 69.4 to 93.1%, showing fair or better agreement (κ ≥ 0.21). In CUP, PD-L1 positivity varied depending on antibodies and scoring systems, with no difference observed according to histologic or clinical subtypes.

摘要

我们研究了程序性死亡配体 1(PD-L1)在不明原发癌(CUP)中的表达及其潜在意义。为 72 例 CUP 病例(组织学亚型:22 例腺癌、15 例低分化癌、19 例鳞状细胞癌和 14 例未分化癌;临床亚型:有利型 17 例[23.6%],不利型 55 例[76.4%])构建了组织微阵列,并进行了 PD-L1(22C3、SP142、SP263 和 28-8)、CK7 和 CK20 的免疫组织化学染色,以确定染色结果与临床病理参数之间的关系。在 CUP 中,使用不同的 22C3(TPS≥1%,CPS≥10%)、SP142(TC≥50%,IC≥10%)、SP263 和 28-8(TC 和 IC≥1%)的截断值,PD-L1 阳性率为 5.6%-48.6%(肿瘤细胞[TC]或肿瘤比例评分[TPS]:5.6%-36.1%,免疫细胞评分[IC]:8.3%-48.6%,联合阳性评分[CPS]:16.7%)。PD-L1 SP142 TC 和 PD-L1 SP263 IC 的阳性率最低(5.6%)和最高(48.6%)。PD-L1 阳性率与克隆的组织学亚型、临床亚型或 CK7/CK20 无关。考虑到 TCκ≥1%、TCκ≥50%、ICκ≥1%和 ICκ≥10%,PD-L1 阳性率为 TC=4.2-36.1%和 IC=9.7-48.6%;抗体之间的总体一致性为 69.4%至 93.1%,显示出良好或更好的一致性(κ≥0.21)。在 CUP 中,PD-L1 阳性率因抗体和评分系统而异,与组织学或临床亚型无关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27c8/11155179/f958f1fa3bc0/12885_2024_12437_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27c8/11155179/2c0a6a788c88/12885_2024_12437_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27c8/11155179/f958f1fa3bc0/12885_2024_12437_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27c8/11155179/2c0a6a788c88/12885_2024_12437_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27c8/11155179/f958f1fa3bc0/12885_2024_12437_Fig2_HTML.jpg

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3
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Pathol Res Pract. 2022 May;233:153893. doi: 10.1016/j.prp.2022.153893. Epub 2022 Apr 12.
4
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Future Oncol. 2021 Aug;17(22):2893-2905. doi: 10.2217/fon-2021-0092. Epub 2021 Jun 30.
6
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Front Med (Lausanne). 2021 May 7;8:668612. doi: 10.3389/fmed.2021.668612. eCollection 2021.
7
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8
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