Brown Jacqueline T, Liu Yuan, Shabto Julie M, Martini Dylan J, Ravindranathan Deepak, Hitron Emilie Elise, Russler Greta Anne, Caulfield Sarah, Yantorni Lauren Beth, Joshi Shreyas S, Kissick Haydn, Ogan Kenneth, Harris Wayne B, Carthon Bradley C, Kucuk Omer, Master Viraj A, Bilen Mehmet Asim
Department of Hematology and Medical Oncology, Emory University School of Medicine, Atlanta, Georgia, USA.
Winship Cancer Institute, Emory University, Atlanta, Georgia, USA.
Oncologist. 2021 May;26(5):397-405. doi: 10.1002/onco.13727. Epub 2021 Mar 18.
The modified Glasgow prognostic score (mGPS), a clinical tool that incorporates albumin and C-reactive protein, has proven useful in the prognostication of multiple cancers. Several immune checkpoint inhibitors (ICIs) have been approved for the treatment of metastatic urothelial cell carcinoma (mUC), but a prognostic biomarker is needed. We investigated the impact of mGPS on survival outcomes in patients with mUC receiving ICIs.
We retrospectively reviewed patients with mUC treated with ICIs (programmed cell death protein 1 or programmed cell death ligand 1 inhibitors) at Winship Cancer Institute from 2015 to 2018. Overall survival (OS) and progression-free survival (PFS) were measured from the start date of ICI until death or clinical or radiographic progression, respectively. mGPS was defined as a summary score with one point given for C-reactive protein >10 mg/L and/or albumin <3.5 g/dL. Univariate (UVA) and multivariate (MVA) analyses were carried out using Cox proportional hazard model. These outcomes were also assessed by Kaplan-Meier analysis.
A total of 53 patients were included with a median follow-up 27.1 months. The median age was 70 years, with 84.9% male and 20.8% Black. Baseline mGPS was 0 in 43.4%, 1 in 28.3% and 2 in 28.3%. Increased mGPS at the time of ICI initiation was associated with poorer OS and PFS in UVA, MVA, and Kaplan-Meier analyses.
The mGPS may be a useful prognostic tool in patients with mUC when treatment with ICI is under consideration. These results warrant a larger study for validation.
The ideal prognostic tool for use in a busy clinical practice is easy-to-use, cost-effective, and capable of accurately predicting clinical outcomes. There is currently no universally accepted risk score in metastatic urothelial cell carcinoma (mUC), particularly in the immunotherapy era. The modified Glasgow prognostic score (mGPS) incorporates albumin and C-reactive protein and may reflect underlying chronic inflammation, a known risk factor for resistance to immune checkpoint inhibitors (ICIs). This study found that baseline mGPS is associated with survival outcomes in patients with mUC treated with ICIs and may help clinicians to prognosticate for their patients beginning immunotherapy.
改良格拉斯哥预后评分(mGPS)是一种结合了白蛋白和C反应蛋白的临床工具,已被证明在多种癌症的预后评估中有用。几种免疫检查点抑制剂(ICI)已被批准用于治疗转移性尿路上皮癌(mUC),但仍需要一种预后生物标志物。我们研究了mGPS对接受ICI治疗的mUC患者生存结果的影响。
我们回顾性分析了2015年至2018年在温希普癌症研究所接受ICI(程序性细胞死亡蛋白1或程序性细胞死亡配体1抑制剂)治疗的mUC患者。总生存期(OS)和无进展生存期(PFS)分别从ICI开始日期测量至死亡或临床或影像学进展。mGPS被定义为一个综合评分,C反应蛋白>10mg/L和/或白蛋白<3.5g/dL各得1分。使用Cox比例风险模型进行单因素(UVA)和多因素(MVA)分析。这些结果也通过Kaplan-Meier分析进行评估。
共纳入53例患者,中位随访时间为27.1个月。中位年龄为70岁,男性占84.9%,黑人占20.8%。基线mGPS为0的占43.4%,为1的占28.3%,为2的占28.3%。在UVA、MVA和Kaplan-Meier分析中,ICI开始时mGPS升高与较差的OS和PFS相关。
在考虑使用ICI治疗时,mGPS可能是mUC患者有用的预后工具。这些结果需要更大规模的研究进行验证。
在繁忙的临床实践中使用的理想预后工具应易于使用、具有成本效益且能够准确预测临床结果。目前在转移性尿路上皮癌(mUC)中没有普遍接受的风险评分,特别是在免疫治疗时代。改良格拉斯哥预后评分(mGPS)结合了白蛋白和C反应蛋白,可能反映潜在的慢性炎症,这是已知的对免疫检查点抑制剂(ICI)耐药的风险因素。本研究发现基线mGPS与接受ICI治疗的mUC患者的生存结果相关,可能有助于临床医生对开始免疫治疗的患者进行预后评估。