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感应热化疗可提高对小鼠纤维肉瘤进行分次放射治疗时的治疗增益因子。

Induction thermochemotherapy increases therapeutic gain factor for the fractionated radiotherapy given to a mouse fibrosarcoma.

作者信息

Kuroda M, Urano M, Nishimura Y, Reynolds R

机构信息

Department of Radiation Medicine, University of Kentucky Medical Center, Lexington, USA.

出版信息

Int J Radiat Oncol Biol Phys. 1997 May 1;38(2):411-7. doi: 10.1016/s0360-3016(97)00037-0.

Abstract

PURPOSE

It has been shown that thermochemotherapy (TC) given prior to radiation reduces the number of clonogens, with a resultant decrease in the tumor control radiation dose. The purpose of this article was to investigate using an animal tumor model how this clonogen reduction affects subsequent fractionated radiotherapy, including repopulation of surviving clonogens, and whether the induction TC can increase the therapeutic gain factor (TGF).

METHODS AND MATERIALS

The single-cell suspensions prepared from the fourth-generation isotransplants of a spontaneous fibrosarcoma, FSa-II, were transplanted into the C3Hf/Sed mouse foot. TC was given by heating tumors at 41.5 degrees C for 30 min immediately after an intraperitoneal injection of cyclophosphamide (200 mg/kg) when tumors reached an average diameter of 4 mm. Fractionated radiotherapy (R) with equally graded daily doses was initiated 24 h after TC either in air (A) or under hypoxic conditions (H). The 50% tumor control dose (TCD50) and the radiation dose to induce a score 2.0 reaction (complete epilation with fibrosis) in one-half of irradiated animals, RD50(2.0), were obtained, and the TGF was calculated. Our previous results on the fractionated radiotherapy using the same tumor system served as controls.

RESULTS

The TCD50(A, single dose) and TCD50(H, single dose) following TC+R were 52.2 and 57.3 Gy, respectively, which were 14.0 and 20.4 Gy lower than those following radiation alone. The TCD50(A, TC+R) increased only slightly when the number of fractions was increased from one to 10 doses, and all TCD50s were significantly lower than the TCD50(A, R alone). Both TCD50(H, TC+R) and TCD50(H, R alone) increased consistently from a single dose to 20 doses, but all TCD50(H, TC+R) were significantly lower than the TCD50(H, R alone). Regarding the normal tissue reaction, the RD50 values both following TC+R and R alone increased consistently from a single dose to 20 daily doses. However, the RD50(TC+R) and RD50(R alone) for each corresponding number of fractions was not significantly different, resulting in the TGFs significantly > 1.0 for combined TC+R treatments, with the exception of 20 daily doses given in air.

CONCLUSION

The induction TC decreased the TCD50 values substantially without altering the RD50 for a late reaction, resulting in an significant increase in the TGF. These results encourage the use of TC as an induction treatment prior to fractionated radiotherapy.

摘要

目的

研究表明,放疗前给予热化疗(TC)可减少克隆源性细胞数量,从而降低肿瘤控制所需的放射剂量。本文旨在利用动物肿瘤模型研究这种克隆源性细胞数量减少如何影响后续的分次放射治疗,包括存活克隆源性细胞的再增殖,以及诱导性热化疗是否能提高治疗增益因子(TGF)。

方法与材料

将自发纤维肉瘤FSa-II第四代同基因移植瘤制备的单细胞悬液接种于C3Hf/Sed小鼠足部。当肿瘤平均直径达到4mm时,腹腔注射环磷酰胺(200mg/kg)后立即将肿瘤加热至41.5℃ 30分钟进行热化疗。热化疗后24小时,在空气(A)或缺氧条件(H)下开始给予等剂量分级的分次放射治疗(R)。获得50%肿瘤控制剂量(TCD50)以及使一半受照射动物出现2.0级反应(完全脱毛伴纤维化)的放射剂量RD50(2.0),并计算治疗增益因子。我们之前使用相同肿瘤系统进行分次放射治疗的结果作为对照。

结果

热化疗联合放疗后,单剂量照射时的TCD50(A)和TCD50(H)分别为52.2 Gy和57. Gy,比单纯放疗时分别低14.0 Gy和20.4 Gy。当分次剂量从1次增加到次时,TCD50(A, 热化疗联合放疗)仅略有增加,且所有TCD50均显著低于单纯放疗时的TCD50(A)。TCD50(H, 热化疗联合放疗)和TCD50(H, 单纯放疗)均从单剂量到20次剂量持续增加,但所有TCD50(H, 热化疗联合放疗)均显著低于单纯放疗时的TCD50(H)。关于正常组织反应,热化疗联合放疗和单纯放疗后的RD50值均从单剂量到每日20次剂量持续增加。然而,各相应分次剂量下的RD50(热化疗联合放疗)和RD50(单纯放疗)无显著差异,导致热化疗联合放疗治疗时的治疗增益因子显著>1.0,但空气环境下每日20次剂量照射除外。

结论

诱导性热化疗可显著降低TCD50值,而不改变晚期反应的RD50,从而使治疗增益因子显著增加。这些结果鼓励在分次放射治疗前使用热化疗作为诱导治疗。

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