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米托蒽醌单独及联合全身热疗对犬淋巴瘤的I期评估。

Phase I evaluation of mitoxantrone alone and combined with whole body hyperthermia in dogs with lymphoma.

作者信息

Hauck M L, Price G S, Ogilvie G K, Johnson J, Gillette E L, Thrall D E, Dewhirst M W, Page R L

机构信息

Duke University Medical Center, Durham, NC, USA.

出版信息

Int J Hyperthermia. 1996 May-Jun;12(3):309-20. doi: 10.3109/02656739609022520.

DOI:10.3109/02656739609022520
PMID:9044901
Abstract

The maximum tolerated dose of mitoxantrone (MX) administered alone or combined with whole body hyperthermia (WBH) was determined in this nonrandomized, prospective study in dogs with lymphoma. MX was administered to 53 dogs every three weeks for a total of six treatments unless progressive disease or persistent, severe toxicity developed. Fifty dogs were evaluable (MX alone n = 30, MX/WBH n = 20). MX was administered as a 1 h infusion at the onset of the plateau phase of WBH in dogs treated with combined therapy. Dogs were evaluated weekly between treatments for the first four treatments with physical examination and complete blood counts to define acute and cumulative toxicity. Dogs were evaluated every three weeks for tumour response until relapse. The maximum tolerated dose (MTD) was defined as that dose in each group that resulted in a 50% incidence of moderate or severe toxicity as estimated from logistic regression analysis of the toxicity data. Myelosuppression was the only toxicity observed. Neutropenia was equal in frequency and severity between treatment groups. Thrombocytopenia was not observed in any dog receiving MX/WBH but occurred in 13% of dogs treated with MX alone. The MTD for MX +/- WBH was 6.1 +/- 0.6 and 6.5 +/- 0.8mg/M2 respectively. A steeper dose response relationship was observed in dogs receiving combined therapy compared to dogs treated with MX alone suggesting WBH may improve the uniformity of patient response to chemotherapy. We concluded that MX may be administered without dose reduction to dogs undergoing WBH and that MX should be evaluated more thoroughly in future thermochemotherapy studies.

摘要

在这项针对淋巴瘤犬的非随机前瞻性研究中,确定了单独使用米托蒽醌(MX)或与全身热疗(WBH)联合使用时的最大耐受剂量。除非出现疾病进展或持续的严重毒性,否则每三周给53只犬使用MX,共进行六次治疗。50只犬可进行评估(单独使用MX组n = 30,MX/WBH组n = 20)。在接受联合治疗的犬中,MX在WBH平台期开始时进行1小时输注。在最初四次治疗期间,每周对犬进行评估,通过体格检查和全血细胞计数来确定急性和累积毒性。每三周对犬进行肿瘤反应评估,直至复发。最大耐受剂量(MTD)定义为根据毒性数据的逻辑回归分析估计,每组中导致中度或重度毒性发生率为50%的剂量。观察到的唯一毒性是骨髓抑制。各治疗组之间中性粒细胞减少的频率和严重程度相同。接受MX/WBH的犬未观察到血小板减少,但单独接受MX治疗的犬中有13%出现血小板减少。MX +/- WBH的MTD分别为6.1 +/- 0.6和6.5 +/- 0.8mg/M2。与单独接受MX治疗的犬相比,接受联合治疗的犬观察到更陡峭的剂量反应关系,这表明WBH可能会改善患者对化疗反应的一致性。我们得出结论,对于接受WBH的犬,可以不减量使用MX,并且在未来的热化疗研究中应更全面地评估MX。

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