在卵巢癌的多个测试中编程死亡-连接体1表达:比较分析
Eun Bi Jang1, Kyeong A So1, Wook Youn Kim2
1Department of Obstetrics and Gynecology, Research Institute of Medical Science, Konkuk University School of Medicine, Seoul, Korea.
Cancer research and treatment
|June 12, 2025
概括
在卵巢癌中评估编程细胞死亡配体1 (PD-L1) 表达,在测试之间显示出显著的变异性. 化疗可以增加PD-L1阳性,影响免疫检查点抑制剂 (ICI) 治疗决策.
科学领域:
- 在瘤学瘤学.
- 免疫学 免疫学 免疫学
- 病理学 病理学 病理学
背景情况:
- 卵巢癌的治疗具有挑战性,对免疫检查点抑制剂 (ICI) 的反应有限.
- 编程细胞死亡连接体1 (PD-L1) 试验和切断值的标准化缺乏,使临床决策复杂化.
- PD-L1表达是ICI疗效的一个关键生物标志物.
研究的目的:
- 为了评估通常使用的PD-L1免疫组织化学分析在卵巢癌中的一致性.
- 评估化疗后PD-L1表达的变化.
- 在卵巢癌中为PD-L1提供标准化测试协议的信息.
主要方法:
- 分析了29个卵巢癌组织样本,使用了五个经过验证的PD-L1试验 (Dako 22C3,Ventana SP263,Ventana SP142,Dako 28-8,Ventana 22C3).
- 使用组合阳性得分 (CPS),免疫细胞 (IC) 或瘤比例得分 (TPS) 在1%,5%和10%的截止值评估PD-L1阳性.
- 协同分析 (OPA,科恩卡帕) 和化疗前与后的PD-L1表达评估.
主要成果:
- 在1%的CPS切线下,PD-L1阳性率从15.8% (SP142) 到29.8% (Dako 22C3,SP263) 不同.
- SP142测定显示出最低的一致性;Dako 22C3显示出与SP263,28-8和Ventana 22C3.3的高度一致性.
- 化疗增加了PD-L1阳性,28%的患者从阴性转化为阳性.
结论:
- 卵巢癌PD-L1表达是测试依赖的,突出了对标准化测试的需要.
- 化疗后增加PD-L1表达对于指导ICI治疗时间至关重要.
- 需要进一步的研究来验证发现,并完善PD-L1测试的临床应用.
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