Dörr W, Spekl K, Farrell C L
Klinik and Poliklinik für Strahlentherapie and Radioonkologie, Medizinische fakultät Carl Gustav Carus der Technishen Universität, D-01307 Dresden, Germany.
Cell Prolif. 2002 Aug;35 Suppl 1(Suppl 1):86-92. doi: 10.1046/j.1365-2184.35.s1.9.x.
The purpose of this study was to examine the effect of recombinant human keratinocyte growth factor (rHuKGF) on clinically manifest acute oral mucositis. The animal model utilized in this investigation was ventral tongue epithelium of C3H/Neu mice. In a first experiment, graded single doses were applied in order to define dose effect and time course of acute mucosal ulceration, as a clinically relevant endpoint. Irradiation was given to a 3 x 3 mm2 test field in the centre of the ventral tongue with 25 kV X-rays. A single dose of 18 Gy, i.e. a dose after which ulceration is expected in more than 99% of the animals, was applied in subsequent experiments. In the study group of 20 animals, rHuKGF was applied at a daily dose of 5 mg/kg subcutaneously from the time of first diagnosis of ulcer for a maximum of 5 days. In the control group, phosphate-buffered saline was used as a placebo. The time course of ulceration, i.e. individual ulcer duration, was analysed in both the control group without rHuKGF and the study group. Irradiation with graded single doses yielded an ED50 of 11.5 +/- 0.7 Gy (logit analysis). In responding animals, the latent time to first diagnosis of ulceration and the individual ulcer duration were independent of dose. Mean latency (+/- standard deviation) was 10.5 +/- 0.5 days, mean ulcer duration 3.9 +/- 0.6 days for doses 11, 13 and 16 Gy. After a dose of 18 Gy, 39 animals developed ulceration after a mean latency of 9.3 +/- 0.3 days (control and KGF-treated). The average ulcer duration was 4.2 +/- 0.9 days in the placebo group and 4.8 +/- 0.8 days in the KGF group (P = 0.02). We conclude that when rHuKGF treatment is delayed until radiation-induced ulcers are manifest, the therapeutic activity previously reported with other treatment schedules was not observed and there was a slight prolongation of duration of ulceration. These data suggest that during tumour radiotherapy, effective rHuKGF therapy schedules should include administration before the onset of ulcerative mucositis.
本研究的目的是检验重组人角质形成细胞生长因子(rHuKGF)对临床明显的急性口腔黏膜炎的影响。本研究采用的动物模型是C3H/Neu小鼠的腹侧舌上皮。在第一个实验中,给予分级单次剂量以确定急性黏膜溃疡的剂量效应和时间进程,将其作为一个临床相关终点。用25 kV X射线对腹侧舌中央3×3 mm2的测试区域进行照射。在后续实验中给予18 Gy的单次剂量,即预计超过99%的动物会出现溃疡的剂量。在20只动物的研究组中,从首次诊断出溃疡时起,以5 mg/kg的每日剂量皮下注射rHuKGF,最长注射5天。在对照组中,使用磷酸盐缓冲盐水作为安慰剂。对未使用rHuKGF的对照组和研究组的溃疡时间进程,即个体溃疡持续时间进行了分析。分级单次剂量照射产生的半数有效剂量(ED50)为11.5±0.7 Gy(对数分析)。在出现反应的动物中,首次诊断出溃疡的潜伏期和个体溃疡持续时间与剂量无关。对于11、13和16 Gy的剂量,平均潜伏期(±标准差)为10.5±0.5天,平均溃疡持续时间为3.9±0.6天。给予18 Gy剂量后,39只动物在平均潜伏期9.3±0.3天(对照组和KGF治疗组)后出现溃疡。安慰剂组的平均溃疡持续时间为4.2±0.9天,KGF组为4.8±0.8天(P = 0.02)。我们得出结论,当rHuKGF治疗延迟至辐射诱导的溃疡出现时,未观察到先前其他治疗方案所报告的治疗活性,且溃疡持续时间略有延长。这些数据表明,在肿瘤放射治疗期间,有效的rHuKGF治疗方案应包括在溃疡性黏膜炎发作之前给药。