Suppr超能文献

高血清可溶性程序性死亡配体1水平与霍奇金淋巴瘤预后不良相关。

High Serum Level of Soluble Programmed Death Ligand 1 is Associated With a Poor Prognosis in Hodgkin Lymphoma.

作者信息

Guo Xiaofang, Wang Juan, Jin Jietian, Chen Hao, Zhen Zijun, Jiang Wenqi, Lin Tongyu, Huang Huiqiang, Xia Zhongjun, Sun Xiaofei

机构信息

State Key Laboratory of Oncology in South China, Collaborative Innovation Center of Cancer Medicine, Department of Pediatric Oncology, Sun Yat-Sen University Cancer Center, Guangzhou, China; The Eastern Hospital of the First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, China.

State Key Laboratory of Oncology in South China, Collaborative Innovation Center of Cancer Medicine, Department of Pediatric Oncology, Sun Yat-Sen University Cancer Center, Guangzhou, China.

出版信息

Transl Oncol. 2018 Jun;11(3):779-785. doi: 10.1016/j.tranon.2018.03.012. Epub 2018 Apr 24.

Abstract

Blockade of the programmed cell death 1-programmed cell death ligand 1 pathway is a new and promising therapeutic approach in Hodgkin lymphoma (HL). To our knowledge, the impact of soluble programmed cell death ligand 1 (sPD-L1) serum levels on HL patient prognosis has not yet been investigated. In this study, the prognostic value of sPD-L1 was assessed in patients with HL. We measured serum sPD-L1 levels and identified their prognostic value in 108 newly diagnosed HL patients using an enzyme-linked immunosorbent assay (ELISA). We found higher serum sPD-L1 concentrations in HL patients than in healthy controls. The best sPD-L1 cutoff value for predicting disease progression risk was 25.1674 ng/ml. The 4-year progression-free survival (PFS) rates for the high-sPD-L1 and low-sPD-L1 groups were 78.8% and 93.3%, respectively. Multivariate survival analysis showed that advanced stage and higher sPD-L1 levels (>25.1674 ng/ml) were independent prognostic factors for shorter PFS. In addition, higher sPD-L1 levels were positively correlated with advanced stage and negatively correlated with peripheral blood monocyte number. The serum sPD-L1 level is an independent prognostic factor for PFS in HL patients and may allow identification of a subgroup of patients who require more intensive therapy and who may benefit from anti-PD-1 agents.

摘要

程序性细胞死亡蛋白1-程序性细胞死亡配体1通路的阻断是霍奇金淋巴瘤(HL)一种新的且有前景的治疗方法。据我们所知,可溶性程序性细胞死亡配体1(sPD-L1)血清水平对HL患者预后的影响尚未得到研究。在本研究中,评估了sPD-L1在HL患者中的预后价值。我们使用酶联免疫吸附测定(ELISA)测量了108例新诊断HL患者的血清sPD-L1水平,并确定了其预后价值。我们发现HL患者的血清sPD-L1浓度高于健康对照。预测疾病进展风险的最佳sPD-L1临界值为25.1674 ng/ml。高sPD-L1组和低sPD-L1组的4年无进展生存率(PFS)分别为78.8%和93.3%。多因素生存分析表明,晚期和较高的sPD-L1水平(>25.1674 ng/ml)是PFS缩短的独立预后因素。此外,较高的sPD-L1水平与晚期呈正相关,与外周血单核细胞数量呈负相关。血清sPD-L1水平是HL患者PFS的独立预后因素,可能有助于识别需要更强化治疗且可能从抗PD-1药物中获益的患者亚组。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea3f/6058012/957294f5ca36/gr1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验