在癌症患者中,贝伐单抗的累积剂量与蛋白尿相关,而与足尿无关

Q1 Medicine
Stephanie Lankhorst PhD , Hans J. Baelde PhD , Jose A.M.C. Verstijnen MSc , Albert J. ten Tije PhD , Marc H.M. Thelen PhD , A.H. Jan Danser PhD , Anton H. van den Meiracker PhD, MD , Mariëtte H.W. Kappers PhD, MD
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引用次数: 1

摘要

血管生成抑制贝伐单抗是一种抗血管内皮生长因子a (VEGF-A)的单克隆抗体,是一种与高血压和肾小球毒性(称为子痫前期样综合征)相关的抗癌治疗方法。在子痫前期,足细胞尿早于蛋白尿和子痫前期的临床特征,被认为是肾小球持续损伤的生物标志物。使用尿中足细胞特异性分子nephrin、足细胞特异性分子podocin和VEGF-A的定量聚合酶链反应,我们检查了贝伐单抗治疗的癌症患者中是否存在足细胞尿,以及它是否与蛋白尿和贝伐单抗的累积剂量有关。横断面收集43例贝伐单抗治疗患者、21例化疗患者和7例健康对照者的尿液样本。贝伐单抗组尿蛋白与肌酐比值(平均值和范围)为32.0 mg/mmol(5.2-284.4),化疗组为11.4 mg/mmol (1.1-21.0), 7.4 mg/mmol (3.9-16.5) (P <3组尿白蛋白/肌酐比值分别为18.9 mg/mmol(0.1 ~ 227.7)、1.5 mg/mmol(0.2 ~ 3.5)和0.2 mg/mmol (0.1 ~ 0.4) (P <. 05)。贝伐单抗的累积剂量范围为550至93,628 mg。59%的参与者尿足素mRNA表达未检测到,每mmol肌酐尿肾素mRNA表达在0.0至5.3之间,尿VEGF-A mRNA表达在0.0至2.7之间。尿肾素mRNA表达与白蛋白与肌酐比值或贝伐单抗累积剂量无关,而后者与白蛋白与肌酐比值相关(r = 0.77;P & lt;措施)。我们的研究结果表明,定量聚合酶链反应技术测量的贝伐单抗累积剂量与蛋白尿密切相关,但与足细胞尿无关,这挑战了这种测量方法监测长期接受贝伐单抗治疗的患者持续肾小球损伤的可行性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cumulative dose of bevacizumab associates with albuminuria rather than podocyturia in cancer patients

Angiogenesis inhibition with bevacizumab, a monoclonal antibody against vascular endothelial growth factor A (VEGF-A), is an anticancer treatment associated with hypertension and renal glomerular toxicity referred to as a preeclampsia-like syndrome. In preeclampsia, podocyturia predates proteinuria and clinical features of preeclampsia, and is regarded as a biomarker of ongoing glomerular injury. Using a quantitative polymerase chain reaction of the podocyte-specific molecules nephrin, podocin, and VEGF-A in the urine, we examined whether podocyturia is present in bevacizumab-treated cancer patients, and whether it relates to proteinuria and the cumulative dose of bevacizumab. Urine samples were cross-sectionally collected from 43 bevacizumab-treated patients, 21 chemotherapy-treated patients, and 7 healthy controls. Urinary protein-to-creatinine ratio (mean and range) was 32.0 mg/mmol (5.2–284.4) in the bevacizumab group, compared with 11.4 mg/mmol (1.1–21.0) in the chemotherapy group and 7.4 mg/mmol (3.9–16.5) (P < .05) in healthy controls, whereas urinary albumin-to-creatinine ratio values in the three groups were, respectively, 18.9 mg/mmol (0.1–227.7), 1.5 mg/mmol (0.2–3.5), and 0.2 mg/mmol (0.1–0.4) (P < .05). The cumulative dose of bevacizumab ranged from 550 to 93,628 mg. Urinary podocin mRNA expression was undetectable in 59% of participants, urinary nephrin mRNA expression per mmol creatinine ranged from 0.0 to 5.3 and urinary VEGF-A mRNA expression from 0.0 to 2.7. Urinary nephrin mRNA expression did not correlate to the albumin-to-creatinine ratio or the cumulative dose of bevacizumab, whereas the latter correlated with the albumin-to-creatinine ratio (r = 0.77; P < .001). Our results demonstrate that the cumulative dose of bevacizumab is closely correlated with albuminuria but not with podocyturia as measured with the quantitative polymerase chain reaction technique, challenging the feasibility of this measurement to monitor ongoing glomerular injury in patients chronically treated with bevacizumab.

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来源期刊
CiteScore
4.80
自引率
0.00%
发文量
0
审稿时长
6.6 weeks
期刊介绍: Cessation. The Journal of the American Society of Hypertension (JASH) publishes peer-reviewed articles on the topics of basic, applied and translational research on blood pressure, hypertension and related cardiovascular disorders and factors; as well as clinical research and clinical trials in hypertension. Original research studies, reviews, hypotheses, editorial commentary and special reports spanning the spectrum of human and experimental animal and tissue research will be considered. All research studies must have been conducted following animal welfare guidelines. Studies involving human subjects or tissues must have received approval of the appropriate institutional committee charged with oversight of human studies and informed consent must be obtained.
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