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C3H小鼠乳腺癌的体内分次热化疗

Fractionated thermochemotherapy in vivo of a C3H mouse mammary carcinoma.

作者信息

Monge O R, Rofstad E K

机构信息

Department of Medical Oncology, Institute for Cancer Research, Norwegian Radium Hospital, Oslo.

出版信息

Radiother Oncol. 1991 Jul;21(3):171-8. doi: 10.1016/0167-8140(91)90034-e.

DOI:10.1016/0167-8140(91)90034-e
PMID:1924852
Abstract

The interaction between fractionated heat treatment and fractionated drug treatment with cyclophosphamide (CTX) was investigated in a transplantable C3H mouse mammary carcinoma inoculated into the hind leg of C3D2F1/Bom mice. A tumour core temperature of 43.5 +/- 0.1 degrees C was achieved by immersing the tumour-bearing leg into a water bath thermostatically maintained at 43.7 +/- 0.1 degrees C. CTX was administered i.p. using the maximum tolerated dose (MTD) (LD 1%) for single fraction treatment (100 mg/kg) as the maximum fraction dose. For combined treatment CTX was given 15 min prior to heating. The endpoint was the time to reach a tumour volume of 5 times the volume at first treatment. Specific growth delay was used as effect parameter. In dose-effect experiments using total treatment time at 43.5 degrees C as dose parameter, drug enhancement ratio (DER) was determined as the ratio of the slope of the dose-effect curve for MTD of CTX plus heat to the slope of the curve for heat alone. In dose-effect experiments using total CTX dose as dose parameter, thermal enhancement ratio (TER) was determined as the ratio of the slope of the dose-effect curve for CTX plus 43.5 degrees C for 30 min to the slope of the curve for CTX alone. The regimens investigated were single fraction treatment and 3 and 5 fractions with time intervals of 3 and 5 days. For single fraction treatment DER was 1.4 +/- 0.1 and TER 2.3 +/- 0.2. The drug sensitization of the effect of heat treatment tended to increase with increasing number of fractions.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在接种于C3D2F1/Bom小鼠后腿的可移植C3H小鼠乳腺癌模型中,研究了分次热处理与环磷酰胺(CTX)分次药物治疗之间的相互作用。将荷瘤腿浸入恒温维持在43.7±0.1℃的水浴中,使肿瘤核心温度达到43.5±0.1℃。CTX通过腹腔注射给药,单次分次治疗的最大耐受剂量(MTD)(LD 1%)(100 mg/kg)作为最大分次剂量。联合治疗时,CTX在加热前15分钟给予。终点指标是肿瘤体积达到首次治疗时体积5倍的时间。将特定生长延迟用作效应参数。在以43.5℃的总治疗时间作为剂量参数的剂量效应实验中,药物增强率(DER)定义为CTX加加热的MTD剂量效应曲线斜率与单独加热曲线斜率之比。在以总CTX剂量作为剂量参数的剂量效应实验中,热增强率(TER)定义为CTX加43.5℃ 30分钟的剂量效应曲线斜率与单独CTX曲线斜率之比。所研究的方案包括单次分次治疗以及间隔3天和5天的3次和5次分次治疗。单次分次治疗的DER为1.4±0.1,TER为2.3±0.2。热处理效果的药物致敏作用倾向于随着分次次数的增加而增强。(摘要截短于250字)

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