Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, SK, Canada.
J Feline Med Surg. 2024 Sep;26(9):1098612X241266418. doi: 10.1177/1098612X241266418.
This retrospective study aimed to determine the incidence and trends of proteinuria, elevations in serum creatinine and urea, and systolic blood pressure in cats undergoing treatment with toceranib.
In total, 32 cats treated with toceranib for malignancies were analyzed. Cats were included if urinalysis and urine protein:creatinine ratio (UPC) measurements were available at 28 days (T1) and 56 days (T2) after starting the treatment. Cats with concurrent lower urinary tract disease, including urinary tract malignancy, were excluded. Friedman's ANOVA compared variables between time points, and the Spearman test assessed the correlation between treatment duration and UPC.
The median starting dose of toceranib was 2.68 mg/kg (range 1.7-3.9). In total, 15 (46.9%) cats received concurrent non-steroidal anti-inflammatory drugs. The most commonly treated tumors were oral squamous cell carcinoma (n = 10) and mast cell tumor (n = 5). None of the 32 cats developed progressive proteinuria or azotemia during the follow-up period (median 56 days; range 56-336). Notably, UPC and serum creatinine were significantly lower at T2 compared with baseline ( = 0.012 and 0.001, respectively). Among the four cats with baseline proteinuria, UPC decreased over time with or without concurrent telmisartan treatment (n = 2). All four of these cats experienced a reduction in tumor size with toceranib concurrently with their decreased UPC. There was no significant correlation between UPC and the duration of toceranib treatment ( = 0.089). Blood pressure was not significantly different over the assessed time points.
The incidence of proteinuria, renal azotemia and hypertension in cats treated with toceranib for neoplasia appears to be low. Toceranib may be a viable treatment option even in cats with pre-existing proteinuria or renal disease, with careful monitoring of trends recommended.
本回顾性研究旨在确定接受托昔单抗治疗的猫发生蛋白尿、血清肌酐和尿素升高以及收缩压升高的发生率和趋势。
共分析了 32 只接受托昔单抗治疗恶性肿瘤的猫。如果在开始治疗后 28 天(T1)和 56 天(T2)有尿液分析和尿蛋白与肌酐比值(UPC)测量值,则将猫纳入研究。排除同时患有下尿路疾病(包括尿路恶性肿瘤)的猫。采用 Friedman ANOVA 比较各时间点的变量,采用 Spearman 检验评估治疗持续时间与 UPC 的相关性。
托昔单抗的起始剂量中位数为 2.68mg/kg(范围 1.7-3.9)。共有 15 只(46.9%)猫同时接受了非甾体抗炎药治疗。最常治疗的肿瘤是口腔鳞状细胞癌(n=10)和肥大细胞瘤(n=5)。在随访期间,32 只猫中没有一只发生进行性蛋白尿或氮质血症(中位随访时间 56 天;范围 56-336 天)。值得注意的是,T2 时 UPC 和血清肌酐与基线相比显著降低( =0.012 和 0.001)。在基线时有蛋白尿的 4 只猫中,UPC 随时间降低,无论是否同时使用替米沙坦治疗(n=2)。这 4 只猫的肿瘤大小均随着托昔单抗治疗的同时减小,其 UPC 也随之降低。UPC 与托昔单抗治疗持续时间之间无显著相关性( =0.089)。在评估的时间点之间,血压无显著差异。
接受托昔单抗治疗肿瘤的猫发生蛋白尿、肾氮质血症和高血压的发生率似乎较低。托昔单抗可能是一种可行的治疗选择,即使在存在蛋白尿或肾脏疾病的猫中,也应密切监测趋势。