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与顺二氨-1,1-环丁烷二羧酸铂(II)(卡铂)联合使用时全身热疗的最佳持续时间。

Optimal duration of whole body hyperthermia when combined with cis-diaminne-1,1-cychlobutane dicarboxylate platinum (II) (carboplatin).

作者信息

Kaneko T, Sakaguchi Y, Makino M, Matsuda H, Strebel F R, Jenkins G N, Bull J M

机构信息

Department of Internal Medicine, University of Texas, Houston 77030, USA.

出版信息

Anticancer Res. 1997 May-Jun;17(3C):1897-901.

PMID:9216642
Abstract

Minimizing normal tissue toxicity can enhance the therapeutic gain of thermochemotherapy. For this purpose, we investigated the optimal duration of whole body hyperthermia (WBH) (41.5 degrees C) when administered simultaneously with carboplatin (CBDCA). Using a transplantable fibrosarcoma in Fischer 344 rats, we measured tumor growth delay (TGD) as well as normal tissue toxicities (body weight loss, thrombocytopenia) induced by various durations of WBH (0.5, 1.0, 1.5, 2.0 or 2.5 hours) when combined with CBDCA (30 mg/kg, i.v.). When combined with CBDCA, 1.0 hour WBH increased the TGD compared to 0.5 hour of WBH, but with WBH durations greater than 1.0 hour, the TGD did not further significantly increase. Measuring CBDCA-induced myelosuppression, the platelet count on day 6 post-treatment decreased from a control mean of 6.8 x 10(8)/ml to 1.8 x 10(8)/ml after 2.5 hour WBH exposure in a duration-dependent manner (p < 0.001). To estimate the specific therapeutic efficacy (STE), we calculated a ratio of TGD to myelosuppression (thrombocytopenia). Compared to other WBH exposure times, 1.0 hour duration of WBH combined with CBDCA produced the highest STE (2.8) and over 1.5 hour duration of WBH did not result in any additional increase in STE. We conclude that 1.0 hour WBH exposure is optimal when combined with CBDCA in order to maximize the therapeutic gain.

摘要

将正常组织毒性降至最低可提高热化学疗法的治疗增益。为此,我们研究了与卡铂(CBDCA)同时给药时全身热疗(WBH)(41.5摄氏度)的最佳持续时间。使用可移植到Fischer 344大鼠体内的纤维肉瘤,我们测量了不同持续时间的WBH(0.5、1.0、1.5、2.0或2.5小时)与CBDCA(30mg/kg,静脉注射)联合使用时诱导的肿瘤生长延迟(TGD)以及正常组织毒性(体重减轻、血小板减少)。与CBDCA联合使用时,1.0小时的WBH与0.5小时的WBH相比增加了TGD,但当WBH持续时间大于1.0小时时TGD并未进一步显著增加。测量CBDCA诱导的骨髓抑制,治疗后第6天的血小板计数在2.5小时WBH暴露后以持续时间依赖性方式从对照平均值6.8×10⁸/ml降至1.8×10⁸/ml(p<0.001)。为了估计特定治疗效果(STE),我们计算了TGD与骨髓抑制(血小板减少)的比值。与其他WBH暴露时间相比,1.0小时的WBH与CBDCA联合使用产生了最高的STE(2.8),并且超过1.5小时的WBH持续时间并未导致STE的任何额外增加。我们得出结论,为了使治疗增益最大化,与CBDCA联合使用时1.0小时的WBH暴露是最佳的。

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