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程序性细胞死亡配体 1 在卵巢透明细胞癌中的影响日益恶化。

The worsening impact of programmed cell death ligand 1 in ovarian clear cell carcinomas.

机构信息

Department of Obstetrics and Gynecology, National Defense Medical College Hospital, 3-2 Namiki, Tokorozawa, Saitama, 359-8513, Japan.

Department of Basic Pathology, National Defense Medical College Hospital, Tokorozawa, Saitama, 359-8513, Japan.

出版信息

Arch Gynecol Obstet. 2022 Dec;306(6):2133-2142. doi: 10.1007/s00404-022-06582-5. Epub 2022 May 4.

Abstract

PURPOSE

To investigate the clinical significance of programmed cell death ligand 1 (PD-L1) expression in ovarian clear cell carcinoma (CCC).

MATERIALS AND METHODS

Patients with CCC who underwent primary surgery at our hospital between 1984 and 2014 were enrolled in this study. PD-L1 and mismatch repair (MMR) protein expression in tumor cells, tumor-infiltrating lymphocytes (TILs), including cluster of differentiation (CD) 8, CD4, forkhead box P3 (FOXP3), programmed cell death 1 (PD-1), and BAF250a, were evaluated using immunohistochemistry. The association between PD-L1 expression, clinicopathological features, prognosis, and expression of several proteins was investigated.

RESULTS

Of the 125 patients with CCC, 17 had negative PD-L1 and 108 had positive PD-L1. Patients with positive PD-L1 expression showed a lower response to chemotherapy (p = 0.01). In addition, patients with positive PD-L1 showed worse progression-free survival (PFS, p = 0.01) and overall survival (OS, p = 0.01) than that in patients with negative PD-L1 expression. Multivariate analyses for PFS and OS showed that PD-L1 expression was an independent prognostic factor for PFS (hazard ratio [HR] 7.81, p < 0.01) and OS (HR 12.90, p < 0.01). PD-L1 expression was not associated with the expression of several TILs or proteins.

CONCLUSION

The expression of PD-L1 was related to a lower response to chemotherapy and worse prognosis in CCC. These results may be useful for the development of new treatments.

摘要

目的

研究程序性死亡配体 1(PD-L1)在卵巢透明细胞癌(CCC)中的表达的临床意义。

材料与方法

本研究纳入了 1984 年至 2014 年期间在我院接受初次手术治疗的 CCC 患者。采用免疫组织化学法检测肿瘤细胞、肿瘤浸润淋巴细胞(TILs)中 PD-L1 和错配修复(MMR)蛋白、包括分化群(CD)8、CD4、叉头框 P3(FOXP3)、程序性细胞死亡 1(PD-1)和 BAF250a 的表达情况。分析 PD-L1 表达与临床病理特征、预后及几种蛋白表达的关系。

结果

在 125 例 CCC 患者中,17 例 PD-L1 阴性,108 例 PD-L1 阳性。PD-L1 阳性表达患者对化疗的反应较差(p=0.01)。此外,PD-L1 阳性表达患者的无进展生存期(PFS,p=0.01)和总生存期(OS,p=0.01)均较 PD-L1 阴性表达患者差。PFS 和 OS 的多因素分析显示,PD-L1 表达是 PFS(风险比[HR]7.81,p<0.01)和 OS(HR 12.90,p<0.01)的独立预后因素。PD-L1 表达与几种 TILs 或蛋白的表达无关。

结论

PD-L1 的表达与 CCC 患者对化疗的反应降低和预后不良有关。这些结果可能有助于开发新的治疗方法。

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