S B Schneider, R D Nishimura, R P Zimmerman, L Tran, J Shiplacoff, M Tormey, R Contreras, G F Juillard
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引用次数: 0
摘要
我们希望确定非格司汀给予化疗/放疗初期接受外束照射治疗头颈部恶性肿瘤的患者是否会降低口腔/口咽粘膜炎的发生率和严重程度。从放疗的第一天开始,患者随机接受非格拉西汀或安慰剂的皮下注射,并在整个治疗过程中每天持续注射。滴定研究药物以保持中性粒细胞计数在10 × 10(9)和30 × 10(9)/l之间。左、右颊粘膜、硬腭和咽后壁每周评分,由盲法评估者采用两种不同的量表,每周采用最严重的评分进行数据分析。计划的54例患者中有14例是随机的(8例非格昔汀,6例安慰剂),可用于计划的中期分析。使用重复测量方差分析,各组间平均最差评分在不同时间的差异无统计学意义(Hickey, p = 0.231;WHO, p= 0.288)。然而,在几乎所有时间点,非格司汀治疗组的最差平均评分低于安慰剂治疗组,非格司汀治疗组的严重(即3级)粘膜炎评分显著低于安慰剂治疗组。非格司汀可能降低辐射引起的口腔/口咽粘膜炎的严重程度。
Filgrastim (r-metHuG-CSF) and its potential use in the reduction of radiation-induced oropharyngeal mucositis: an interim look at a randomized, double-blind, placebo-controlled trial.
We wished to determine if filgrastim administration to chemotherapy/radiation therapy-naive patients receiving external-beam irradiation for head-and-neck malignancies would reduce the incidence and severity of oral/oropharyngeal mucositis. Patients were randomized to receive subcutaneous injections of either filgrastim or placebo beginning on day 1 of radiation and continuing daily throughout treatment. Study medication was titrated to keep the neutrophil count between 10 x 10(9) and 30 x 10(9)/l. The left and right buccal mucosa, hard palate, and posterior pharyngeal wall were scored weekly, by a blinded evaluator using two different scales, and the most severe score per week was used in data analysis. Fourteen of a planned 54 patients were randomized (8 filgrastim, 6 placebo), and were evaluable for a planned interim analysis. No statistically significant between-group differences were seen in mean worst scores across time using repeated measures analysis of variance (Hickey, p = 0.231; WHO, p= 0.288). At almost all timepoints, however, the worst mean scores were lower in patients treated with filgrastim compared with those in patients treated with placebo, and the number of severe (i.e., grade 3) mucositis scores was significantly lower in the filgrastim-treated group. Filgrastim may decrease the severity of radiation-induced oral/oropharyngeal mucositis.