Cancer Treatment Unit, Department of Veterinary Clinical Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA, USA.
Vet Comp Oncol. 2010 Mar;8(1):11-22. doi: 10.1111/j.1476-5829.2009.00199.x.
The purpose of this study was to evaluate the efficacy of adding mitoxantrone to a cyclophosphamide, doxorubicin, vincristine, L-asparaginase and prednisone containing protocol. Sixty-five dogs with multicentric lymphoma were evaluated for overall remission and survival times. Remission and survival time versus stage, substage, pretreatment hypercalcaemia and pretreatment steroid administration were also evaluated. Overall median remission for dogs with multicentric lymphoma was 302 days and overall median survival was 622 days. Of the dogs with multicentric lymphoma, 23 (35%) received all scheduled mitoxantrone doses. Only median survival versus substage was found to be significant (substage a median survival was 679 days and substage b median survival was 302 days, P = 0.025). Increasing the total combined dose of doxorubicin and mitoxantrone may improve remission times when compared with historical controls, and further studies are needed to determine how best to utilize mitoxantrone in multidrug chemotherapy protocols for canine multicentric lymphoma.
本研究旨在评估在环磷酰胺、阿霉素、长春新碱、L-门冬酰胺酶和泼尼松方案中添加米托蒽醌的疗效。对 65 例患有多中心淋巴瘤的狗进行了总体缓解率和生存时间评估。还评估了缓解和生存时间与分期、亚分期、治疗前高钙血症和治疗前皮质类固醇治疗的关系。多中心淋巴瘤狗的总体中位缓解时间为 302 天,总体中位生存时间为 622 天。在患有多中心淋巴瘤的狗中,有 23 只(35%)接受了所有计划的米托蒽醌剂量。只有亚分期与生存中位数之间存在显著差异(亚分期 a 的中位生存时间为 679 天,亚分期 b 的中位生存时间为 302 天,P=0.025)。与历史对照相比,增加多柔比星和米托蒽醌的总联合剂量可能会改善缓解时间,需要进一步研究以确定如何最好地将米托蒽醌用于犬多中心淋巴瘤的多药化疗方案。