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Pharmacokinetic study and evaluation of the safety of taurolidine for dogs with osteosarcoma

机译:牛磺酸对狗骨肉瘤的安全性的药代动力学研究和评价

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Background Osteosarcoma in dogs and humans share many similarities and the dog has been described as an excellent model to study this disease. The median survival in dogs has not improved in the last 25?years. Taurolidine has been shown to be cytotoxic to canine and human osteosarcoma in vitro. The goals of this study were to determine the pharmacokinetics and safety of taurolidine in healthy dogs and the safety of taurolidine in combination with doxorubicin or carboplatin in dogs with osteosarcoma. Methods Two percent taurolidine was infused into six healthy dogs (150?mg/kg) over a period of two hours and blood samples were taken periodically. One dog received taurolidine with polyvinylpyrrolidone (PVP) as its carrier and later received PVP-free taurolidine as did all other dogs in this study. Serum taurolidine concentrations were determined using high-performance liquid chromatography (HPLC) online coupled to ESI-MS/MS in the multiple reaction monitoring mode. Subsequently, the same dose of taurolidine was infused to seven dogs with osteosarcoma also treated with doxorubicin or carboplatin. Results Taurolidine infusion was safe in 6 healthy dogs and there were no significant side effects. Maximum taurolidine serum concentrations ranged between 229 to 646?μM. The dog that received taurolidine with PVP had an immediate allergic reaction but recovered fully after the infusion was stopped. Three additional dogs with osteosarcoma received doxorubicin and taurolidine without PVP. Toxicities included dilated cardiomyopathy, protein-losing nephropathy, renal insufficiency and vasculopathy at the injection site. One dog was switched to carboplatin instead of doxorubicin and an additional 4 dogs with osteosarcoma received taurolidine-carboplatin combination. One incidence of ototoxicity occurred with the taurolidine- carboplatin combination. Bone marrow and gastro-intestinal toxicity did not appear increased with taurolidine over doxorubicin or carboplatin alone. Conclusions Taurolidine did not substantially exacerbate bone marrow or gastro-intestinal toxicity however, it is possible that taurolidine increased other toxicities of doxorubicin and carboplatin. Administering taurolidine in combination with 30?mg/m2 doxorubicin in dogs is not recommended but taurolidine in combination with carboplatin (300?mg/m2) appears safe.
机译:背景技术狗和人的骨肉瘤具有许多相似之处,并且狗被描述为研究该疾病的极佳模型。在过去的25年中,狗的中位生存期没有改善。牛磺酸在体外对犬和人骨肉瘤具有细胞毒性。这项研究的目的是确定牛磺酸对健康犬的药代动力学和安全性,以及牛磺酸与阿霉素或卡铂联合在骨肉瘤犬中的安全性。方法在两个小时的时间内,向6只健康犬(150?mg / kg)中注入2%的taurolidine,并定期采集血样。一只狗接受以聚乙烯吡咯烷酮(PVP)为载体的taurolidine,后来像本研究中的所有其他狗一样接受不含PVP的taurolidine。使用多反应监测模式在线连接ESI-MS / MS的高效液相色谱(HPLC)测定血清牛磺酸的浓度。随后,向同样用阿霉素或卡铂治疗的骨肉瘤的七只狗中输注了相同剂量的牛磺洛定。结果牛磺啶输注对6只健康犬是安全的,无明显副作用。牛磺酸的最大血清浓度范围为229至646?M。接受PVP的taurolidine的狗有立即过敏反应,但在停止输注后已完全康复。另外三只患有骨肉瘤的狗接受了阿霉素和牛磺酸去氧核糖核酸而没有PVP。毒性包括注射部位的扩张型心肌病,蛋白丢失性肾病,肾功能不全和血管病变。一只狗改用卡铂代替阿霉素,另外四只患有骨肉瘤的狗接受了牛磺吡啶-卡铂联合治疗。牛磺酸-卡铂组合发生了一种耳毒性。牛磺酸与单独的阿霉素或卡铂相比,没有出现骨髓和胃肠道毒性的增加。结论牛磺洛定基本上没有加重骨髓或胃肠道毒性,但是,牛磺洛定有可能增加阿霉素和卡铂的其他毒性。不建议在犬中与牛磺酸联用30?mg / m 2 阿霉素,但与牛磺酸联用卡铂(300?mg / m 2 )似乎是安全的。

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