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血清乳酸脱氢酶在纳武利尤单抗治疗前可能是转移性透明细胞肾细胞癌患者的治疗预后生物标志物。

Serum Lactate Dehydrogenase Before Nivolumab Treatment Could Be a Therapeutic Prognostic Biomarker for Patients With Metastatic Clear Cell Renal Cell Carcinoma.

机构信息

Department of Uro-Oncology, Saitama Medical University International Medical Center, Hidaka, Japan

Department of Urology, Keio University School of Medicine, Tokyo, Japan.

出版信息

Anticancer Res. 2019 Aug;39(8):4371-4377. doi: 10.21873/anticanres.13606.

Abstract

BACKGROUND/AIM: The purpose of this retrospective study was to identify the predictive biomarkers of response to pretreatment for patients with metastatic renal cell carcinoma (mRCC) treated with nivolumab.

MATERIALS AND METHODS

The subjects were 54 patients treated with nivolumab for mRCC with a clear cell component (mccRCC) between September 2016 and February 2018. We analyzed the impact of serum biomarkers (lactate dehydrogenase [LDH], neutrophil-to-lymphocyte ratio, and C-reactive protein) on patients treated with nivolumab. We adopted the International Metastatic Renal Cell Carcinoma Database Consortium prognostic model using six clinical factors (0=favorable, 1 or 2=intermediate, 3 to 6=poor risk groups, respectively).

RESULTS

The prognostic risk classification (non-poor vs. poor) and serum LDH levels were correlated with the objective response of nivolumab treatment for mccRCC. Elevated serum LDH levels at baseline were an independent biomarker for progression-free survival (PFS) of mccRCC patients receiving nivolumab [HR=2.268 (95%CI=1.014-5.051), p=0.046]. Notably, high LDH levels were associated with a poorer PFS for patients in the favorable-risk group.

CONCLUSION

Serum LDH levels at baseline before nivolumab treatment were associated with the objective response and clinical outcome of nivolumab treatment.

摘要

背景/目的:本回顾性研究的目的是确定接受纳武利尤单抗治疗的转移性肾细胞癌(mRCC)患者预处理反应的预测生物标志物。

材料和方法

本研究纳入了 2016 年 9 月至 2018 年 2 月期间接受纳武利尤单抗治疗的 54 例具有透明细胞成分(mccRCC)的 mRCC 患者。我们分析了血清生物标志物(乳酸脱氢酶[LDH]、中性粒细胞与淋巴细胞比值和 C 反应蛋白)对接受纳武利尤单抗治疗的患者的影响。我们采用了国际转移性肾细胞癌数据库联盟的预后模型,使用 6 个临床因素(0=有利,1 或 2=中等,3 至 6=不良风险组,分别)。

结果

预后风险分类(非不良与不良)和血清 LDH 水平与 mccRCC 患者接受纳武利尤单抗治疗的客观反应相关。基线时升高的血清 LDH 水平是 mccRCC 患者接受纳武利尤单抗治疗无进展生存(PFS)的独立生物标志物[HR=2.268(95%CI=1.014-5.051),p=0.046]。值得注意的是,高 LDH 水平与有利风险组患者的 PFS 较差相关。

结论

纳武利尤单抗治疗前基线时的血清 LDH 水平与纳武利尤单抗治疗的客观反应和临床结局相关。

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