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机构地区:[1]江苏连云港市第一医院肿瘤科,江苏连云港222002
出 处:《癌症》2001年第4期426-426,共1页Chinese Journal of Cancer
摘 要:目的:研究大剂量三苯氧胺 (Tamoxifen,TAM)提高非小细胞肺癌化疗效果。方法:将 108例患者按信封法随机分入 A、 B、 C、 D组,每组 27例患者, A、 B、 C三组为研究组, D组为对照组。研究组化疗前 3天至化疗最后 1天口服 TAM,共 11天。 TAM剂量 A组为 40 mg,每日 3次; B组为 60 mg,每日 3次; C组 80 mg,每日 3次; D组单纯化疗。每组化疗用药相同,均为长春碱酰胺 2.5 mg/m2 d1、 d8,阿霉素 30 mg/m2 d2,顺铂 80 mg/m2分 d4、 d5 2天。每组完成 3周期化疗后休息 30天,复查并评价疗效。结果: A、 B、 C、 D各组有效率分别为: 33.3% (9/27)、 48.1% (13/27)、 55.6% (15/27)、 25.9% (7/27), C组有效率最高, D组有效率最低。将 A、 B、 C三组分别与 D组比较,经统计学处理, A∶ D P >0.05; B∶ D P >0.05; C∶ D P< 0.05,有临床意义。各组化疗副作用无区别,仅 C组中有 4例患者用药 5~ 6天后出现精神症状,停服 TAM 1~ 3天后自动恢复正常。结论:大剂量 TAM有拮抗癌细胞对化疗耐药的作用,其剂量与疗效成正相关。Objective: This study was designed to investigate the chemotherapy effect of high- dose tamoxifen(TAM) in the patients with multidrug- resistant (MDR- 1) non- small cell lung cancer(NSCLC). Methods: A total of 108 patients with refractory NSCLC were divided at random into four groups: A,B,C,and D. Each group contained 27 patients. A,B,and C were study group, D was control group. TAM was given from the third day before chemotherapy up to 11 days dose of TAM for group A: 40 mg, tid;group B: 60 mg, tid;group C: 80 mg, tid;group D: Simple chemotherapy. The dosage and schedule of the chemotherapy regimen was just same in every group: VDS 2.5 mg/m2 d1,d8, ADM 30 mg/m2 d2, DDP 80 mg/m2 d4,d5. The therapeutic effect of each group after having been performed 3 cyeles,and treatment rested 30 days was evaluated. Results:The response rates of the A,B,C,and D group were 33.3% (9/27),48.1% (13/27),55.6% (15/27),25.9% (7/27),respectively. The response rate of group C was the highest and group D was the lowest. Compared group A,B,C with group D,A∶ D P >0.05, the difference did not reach statistical significance; B∶ D P >0.05, the difference did not reach statistical significance; C∶ D P< 0.05,the difference reached statistical significance. The major side effect of chemotherapy had not difference in every group. Only four patients of group C with TAM 240 mg/d developed psychiatric symptom, and TAM was abandoned after symptom automatic extinction. Conclusions: High dose TAM can be safely administered and may inhibit MDR- 1 function. The dose of TAM become positive correlation to it s effect.
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