Murakami R, Baba Y, Nishimura R, Furusawa M, Yokoyama T, Yamashita Y, Takahashi M, Yamashita N, Ono T
Department of Radiology, Kumamoto University School of Medicine, Japan.
Int J Radiat Oncol Biol Phys. 1997 Mar 1;37(4):907-11. doi: 10.1016/s0360-3016(96)00621-9.
In our previous report we described the clinical value of azelastine, an oral antiallergic agent, as an inhibitor of radiation dermatitis. Here we studied the effect of azelastine on normal skin and tumor size after irradiation in a mouse model.
The modifying effects of azelastine on both the degree of radiation dermatitis and antitumoral effect of radiation therapy were investigated in the normal skin as well as in SCC VII tumors of C3H/He mice. The right hind legs, with or without tumors, were irradiated with 20-60 Gy at 0.62 Gy/min. Azelastine was administered via the mouse chow, and acute skin reactions and tumor growth curves were compared between the azelastine and control groups.
The acute skin reactions of the azelastine group were significantly less prominent than those of the control group (p < 0.01). At a dose of 40 Gy the dose modification factors were 1.19-1.25. The tumor growth curves of the azelastine and control groups were almost identical, indicating that the treatment response of irradiation was not affected by administration of azelastine.
Application of azelastine reduces the degree of acute radiation dermatitis without affecting the antitumoral effect of radiation therapy.
在我们之前的报告中,我们描述了口服抗过敏药氮卓斯汀作为放射性皮炎抑制剂的临床价值。在此,我们在小鼠模型中研究了氮卓斯汀对放疗后正常皮肤和肿瘤大小的影响。
在C3H/He小鼠的正常皮肤以及SCC VII肿瘤中,研究了氮卓斯汀对放射性皮炎程度和放射治疗抗肿瘤效果的调节作用。对有或没有肿瘤的右后腿以0.62 Gy/分钟的剂量照射20 - 60 Gy。通过小鼠饲料给予氮卓斯汀,并比较氮卓斯汀组和对照组之间的急性皮肤反应和肿瘤生长曲线。
氮卓斯汀组的急性皮肤反应明显不如对照组突出(p < 0.01)。在40 Gy的剂量下,剂量修正因子为1.19 - 1.25。氮卓斯汀组和对照组的肿瘤生长曲线几乎相同,表明放疗的治疗反应不受氮卓斯汀给药的影响。
应用氮卓斯汀可降低急性放射性皮炎的程度,而不影响放射治疗的抗肿瘤效果。