{"title":"上尿路尿路上皮癌中雄激素受体与 PD-L1 表达的关系","authors":"Yohei Okuda, Taigo Kato, Kazutoshi Fujita, Hiroaki Fushimi, Hiroshi Miyamoto, George J Netto, Norio Nonomura","doi":"10.21873/cgp.20435","DOIUrl":null,"url":null,"abstract":"<p><strong>Background/aim: </strong>The response to immune checkpoint inhibitors (ICIs) or enfortumab vedotin is limited in patients with upper urinary tract urothelial carcinoma (UTUC), and the development of new targeted therapy for UTUC is eagerly needed. Several biomarkers, including programmed cell death-ligand 1 (PD-L1), have already been reported as predictors of response to ICIs therapy for UTUC. Recently, several studies have shown that steroid hormone receptors, including the androgen receptor (AR), are associated with progression of urothelial carcinoma.</p><p><strong>Materials and methods: </strong>We prepared tissue microarrays (TMA) from paraffin blocks of UTUC specimens in 99 non-metastatic UTUC patients who underwent radical nephroureterectomy. 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Among AR-positive cases, patients with absence of PD-L1 expression had significantly lower cancer-specific survival (CSS) than that in PD-L1 expression-positive cases (p=0.049), although PD-L1 expression had no significant impact on CSS in AR-negative cases (p=0.920).</p><p><strong>Conclusion: </strong>Our findings suggest that AR is the promising target for UTUC treatment, especially in PD-L1-negative cases.</p>","PeriodicalId":9516,"journal":{"name":"Cancer Genomics & Proteomics","volume":"21 2","pages":"137-143"},"PeriodicalIF":2.6000,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10905274/pdf/","citationCount":"0","resultStr":"{\"title\":\"Association of Androgen Receptor and PD-L1 Expression in Upper Urinary Tract Urothelial Carcinoma.\",\"authors\":\"Yohei Okuda, Taigo Kato, Kazutoshi Fujita, Hiroaki Fushimi, Hiroshi Miyamoto, George J Netto, Norio Nonomura\",\"doi\":\"10.21873/cgp.20435\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background/aim: </strong>The response to immune checkpoint inhibitors (ICIs) or enfortumab vedotin is limited in patients with upper urinary tract urothelial carcinoma (UTUC), and the development of new targeted therapy for UTUC is eagerly needed. 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引用次数: 0
摘要
背景/目的:上尿路尿路上皮癌(UTUC)患者对免疫检查点抑制剂(ICIs)或恩福单抗维多汀的反应有限,因此急需开发新的UTUC靶向疗法。已有报道称,包括程序性细胞死亡配体1(PD-L1)在内的一些生物标志物可预测UTUC对ICIs疗法的反应。最近,一些研究表明,包括雄激素受体(AR)在内的类固醇激素受体与尿路上皮癌的进展有关:我们从99名接受根治性肾切除术的非转移性UTUC患者的UTUC标本石蜡块中制备了组织芯片(TMA)。通过这些 TMA 切片,我们对 PD-L1 和 AR 进行了免疫组化染色,并检测了肿瘤细胞中 PD-L1 和 AR 的表达水平。此外,我们还分析了这些标记物与UTUC病例临床预后的相关性:99例样本中有24例(24%)PD-L1阳性,20例(20%)患者AR阳性。AR阴性样本的PD-L1表达水平明显高于AR阳性样本(平均值为4.70%对2.55%,P=0.0324)。在AR阳性病例中,没有PD-L1表达的患者的癌症特异性生存率(CSS)明显低于PD-L1表达阳性病例(P=0.049),尽管PD-L1表达对AR阴性病例的CSS没有明显影响(P=0.920):我们的研究结果表明,AR是UTUC治疗的理想靶点,尤其是在PD-L1阴性病例中。
Association of Androgen Receptor and PD-L1 Expression in Upper Urinary Tract Urothelial Carcinoma.
Background/aim: The response to immune checkpoint inhibitors (ICIs) or enfortumab vedotin is limited in patients with upper urinary tract urothelial carcinoma (UTUC), and the development of new targeted therapy for UTUC is eagerly needed. Several biomarkers, including programmed cell death-ligand 1 (PD-L1), have already been reported as predictors of response to ICIs therapy for UTUC. Recently, several studies have shown that steroid hormone receptors, including the androgen receptor (AR), are associated with progression of urothelial carcinoma.
Materials and methods: We prepared tissue microarrays (TMA) from paraffin blocks of UTUC specimens in 99 non-metastatic UTUC patients who underwent radical nephroureterectomy. With these TMA sections, we performed immunohistochemical staining for PD-L1 and AR and examined PD-L1 and AR expression levels in tumor cells. In addition, we analyzed the correlation between these markers and clinical prognosis in UTUC cases.
Results: PD-L1 was positive in 24 (24%) of the 99 samples, whereas AR was positive in 20 (20%) patients. AR-negative samples had significantly higher PD-L1 expression level than that the AR-positive samples (mean value 4.70% versus 2.55%, p=0.0324). Among AR-positive cases, patients with absence of PD-L1 expression had significantly lower cancer-specific survival (CSS) than that in PD-L1 expression-positive cases (p=0.049), although PD-L1 expression had no significant impact on CSS in AR-negative cases (p=0.920).
Conclusion: Our findings suggest that AR is the promising target for UTUC treatment, especially in PD-L1-negative cases.
期刊介绍:
Cancer Genomics & Proteomics (CGP) is an international peer-reviewed journal designed to publish rapidly high quality articles and reviews on the application of genomic and proteomic technology to basic, experimental and clinical cancer research. In this site you may find information concerning the editorial board, editorial policy, issue contents, subscriptions, submission of manuscripts and advertising. The first issue of CGP circulated in January 2004.
Cancer Genomics & Proteomics is a journal of the International Institute of Anticancer Research. From January 2013 CGP is converted to an online-only open access journal.
Cancer Genomics & Proteomics supports (a) the aims and the research projects of the INTERNATIONAL INSTITUTE OF ANTICANCER RESEARCH and (b) the organization of the INTERNATIONAL CONFERENCES OF ANTICANCER RESEARCH.