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首页> 外文期刊>Veterinary and Comparative Oncology >Risk factors for development of sterile haemorrhagic cystitis in canine lymphoma patients receiving oral cyclophosphamide: a case-control study
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Risk factors for development of sterile haemorrhagic cystitis in canine lymphoma patients receiving oral cyclophosphamide: a case-control study

机译:口服环磷酰胺的犬淋巴瘤患者发展无菌性出血性膀胱炎的危险因素:病例对照研究

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摘要

Sterile haemorrhagic cystitis (SHC) is a known risk of cyclophosphamide treatment; however, most canine reports are case series. This case-control study examined risk factors for SHC in dogs with lymphoma receiving oral cyclophosphamide. Twenty-two dogs with SHC and 66 control dogs were identified. On univariate analysis, SHC risk factors included age (P=0.041), induction protocol (P=0.021) and cumulative cyclophosphamide dose (P=0.002). On multivariate analysis, increasing cumulative cyclophosphamide dose was associated with increased risk of SHC and the short' induction protocol (protocol 1) was associated with decreased risk. Controlling for age and induction protocol, odds of SHC increased by 2.21 per 750mgm(-2) increase in cyclophosphamide dose (P=0.001). SHC from oral cyclophosphamide is a predominately delayed toxicity resulting from high cumulative doses.
机译:无菌性出血性膀胱炎(SHC)是已知的环磷酰胺治疗的风险;但是,大多数犬类报告都是病例系列。这项病例对照研究检查了接受口服环磷酰胺的淋巴瘤狗中SHC的危险因素。鉴定出22只患有SHC的狗和66只对照狗。在单因素分析中,SHC危险因素包括年龄(P = 0.041),诱导方案(P = 0.021)和环磷酰胺累积剂量(P = 0.002)。在多变量分析中,增加环磷酰胺的累积剂量与增加SHC的风险有关,而短暂的诱导方案(方案1)与降低的风险有关。控制年龄和诱导方案后,环磷酰胺剂量每增加750mgm(-2),SHC的机率增加2.21(P = 0.001)。口服环磷酰胺引起的SHC主要是由于高累积剂量引起的延迟毒性。

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