Ono K, Uchida I, Uno N, Ohno E, Hirota K, Nakayama T, Ohtuka E, Saburi Y, Kikuchi H, Nasu M
Dept. of Hematology, Almeida Memorial Hospital.
Gan To Kagaku Ryoho. 1999 May;26(6):821-8.
The prevention of nausea, vomiting and appetite loss induced by remission induction chemotherapy for acute myeloid leukemia was compared by randomization between granisetron alone and combination with granisetron plus methylprednisolone. Granisetron was administered at 40 micrograms/kg during chemotherapy, and methylprednisolone was administered concomitantly at 125 mg/body for 3 days or more in the combination group. The single and combination groups comprised 14 and 13 patients, respectively, and there was no significant difference between the background of both groups. To evaluate the effect they were scored according to 4 grades, and evaluated every 24 hours from the start of chemotherapy to 5 days after its completion. The complete inhibition rate of vomiting was as high as 71.4% and 92.3% in the single and combination groups, respectively, showing no significant difference. The grade of vomiting was mild in both groups. Nausea was noted in 71.4% and 46.2%, respectively, and the inhibitory effect tended to be higher in the combination group. Appetite loss developed in 92.9% and 41.7%, respectively, and the prevention effect was clearly higher in the combination group. The prevention effects on nausea 7, 8 and 10 days after the start of chemotherapy, on appetite loss 2-10 days after it, and 2-5 days after its completion, were higher in the combination group. Granisetron revealed an excellent inhibitory effect on vomiting induced by remission induction chemotherapy for acute myeloid leukemia, but combination with granisetron and methylprednisolone was considered useful for nausea in the latter half of the treatment period and for appetite loss during the whole period.
通过随机分组比较了格拉司琼单独使用与格拉司琼联合甲泼尼龙对急性髓系白血病缓解诱导化疗引起的恶心、呕吐和食欲减退的预防效果。化疗期间,格拉司琼以40微克/千克的剂量给药,联合组中甲泼尼龙以125毫克/人伴随给药3天或更长时间。单药组和联合组分别有14例和13例患者,两组的背景无显著差异。为评估效果,根据4个等级进行评分,从化疗开始至结束后5天,每24小时评估一次。单药组和联合组呕吐的完全抑制率分别高达71.4%和92.3%,无显著差异。两组呕吐程度均较轻。恶心发生率分别为71.4%和46.2%,联合组的抑制作用倾向于更高。食欲减退发生率分别为92.9%和41.7%,联合组的预防效果明显更高。联合组在化疗开始后7、8和10天对恶心的预防效果、化疗后2 - 10天对食欲减退的预防效果以及化疗结束后2 - 5天对食欲减退的预防效果均更高。格拉司琼对急性髓系白血病缓解诱导化疗引起的呕吐显示出优异的抑制效果,但格拉司琼与甲泼尼龙联合使用被认为对治疗后半期的恶心以及整个期间的食欲减退有效。