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接受免疫检查点抑制剂治疗的转移性尿路上皮癌患者的新型风险组分层

Novel risk group stratification for metastatic urothelial cancer patients treated with immune checkpoint inhibitors.

作者信息

Shabto Julie M, Martini Dylan J, Liu Yuan, Ravindranathan Deepak, Brown Jacqueline, Hitron Emilie E, Russler Greta A, Caulfield Sarah, Kissick Haydn, Alemozaffar Mehrdad, Ogan Kenneth, Harris Wayne B, Master Viraj A, Kucuk Omer, Carthon Bradley C, Bilen Mehmet A

机构信息

Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, GA, USA.

Winship Cancer Institute of Emory University, Atlanta, GA, USA.

出版信息

Cancer Med. 2020 Apr;9(8):2752-2760. doi: 10.1002/cam4.2932. Epub 2020 Feb 25.

Abstract

BACKGROUND

We developed a novel risk scoring system for urothelial cancer (UC) patients receiving immune checkpoint inhibitors (ICI).

METHODS

We conducted a retrospective review of 67 UC patients treated with ICI at Winship Cancer Institute of Emory University from 2015 to 2018. Using stepwise variable selection in Cox proportional hazard model and Sullivan's weighting schema, baseline platelet-to-lymphocyte ratio (PLR), presence of liver metastasis, baseline albumin, and baseline Eastern Cooperative Oncology Group performance status (ECOG PS) were used for risk scoring. Patients were categorized into good risk (risk score 0-1), intermediate risk (risk score 2-3), and poor risk (risk score 4-6). Univariable (UVA) and multivariable analysis (MVA) and Kaplan-Meier method were used to assess overall survival (OS) and progression free survival (PFS).

RESULTS

The Emory Risk Scoring System had C-statistics of 0.74 (Standard Error = 0.047) in predicting OS and 0.70 (Standard Error = 0.043) in predicting PFS. Compared to good risk patients, poor risk patients had significantly shorter OS and PFS in both UVA and MVA (all P < .001), and intermediate risk patients had significantly shorter OS and PFS in both UVA and MVA (all P < .03).

CONCLUSIONS

Risk scoring using baseline PLR, presence of liver metastasis, baseline albumin, and baseline ECOG PS may effectively predict OS and PFS in UC patients receiving ICI.

摘要

背景

我们为接受免疫检查点抑制剂(ICI)治疗的尿路上皮癌(UC)患者开发了一种新型风险评分系统。

方法

我们对2015年至2018年在埃默里大学温希普癌症研究所接受ICI治疗的67例UC患者进行了回顾性研究。在Cox比例风险模型中使用逐步变量选择和沙利文加权方案,将基线血小板与淋巴细胞比率(PLR)、肝转移情况、基线白蛋白和基线东部肿瘤协作组体能状态(ECOG PS)用于风险评分。患者被分为低风险(风险评分0 - 1)、中风险(风险评分2 - 3)和高风险(风险评分4 - 6)。采用单变量分析(UVA)、多变量分析(MVA)和Kaplan - Meier方法评估总生存期(OS)和无进展生存期(PFS)。

结果

埃默里风险评分系统在预测OS时的C统计量为0.74(标准误 = 0.047),在预测PFS时的C统计量为0.70(标准误 = 0.043)。与低风险患者相比,高风险患者在UVA和MVA中的OS和PFS均显著缩短(所有P < 0.001),中风险患者在UVA和MVA中的OS和PFS也均显著缩短(所有P < 0.03)。

结论

使用基线PLR、肝转移情况、基线白蛋白和基线ECOG PS进行风险评分可有效预测接受ICI治疗的UC患者的OS和PFS。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e47/7163104/f00c5a58b5b1/CAM4-9-2752-g001.jpg

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