Department of Clinical Studies, Matthew J. Ryan Veterinary Hospital, University of Pennsylvania School of Veterinary Medicine, Philadelphia, PA, USA.
Vet Comp Oncol. 2014 Dec;12(4):277-86. doi: 10.1111/vco.12009. Epub 2012 Oct 19.
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 750 mg m(-2) increase in cyclophosphamide dose (P = 0.001). SHC from oral cyclophosphamide is a predominately delayed toxicity resulting from high cumulative doses.
无菌性出血性膀胱炎 (SHC) 是环磷酰胺治疗的已知风险;然而,大多数犬的报告都是病例系列。本病例对照研究检查了接受口服环磷酰胺治疗的淋巴瘤犬发生 SHC 的风险因素。确定了 22 例 SHC 犬和 66 例对照犬。在单因素分析中,SHC 的风险因素包括年龄(P=0.041)、诱导方案(P=0.021)和累积环磷酰胺剂量(P=0.002)。在多因素分析中,累积环磷酰胺剂量增加与 SHC 的风险增加相关,“短”诱导方案(方案 1)与风险降低相关。在控制年龄和诱导方案后,环磷酰胺剂量每增加 750mg/m²,SHC 的发生几率增加 2.21 倍(P=0.001)。口服环磷酰胺引起的 SHC 主要是由于累积剂量高导致的迟发性毒性。