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作 者:周宗玫[1] 王绿化[1] 吕纪马[1] 陈东福[1] 张红星[1] 欧广飞[1] 梁军[1] 殷蔚伯[1]
机构地区:[1]中国医学科学院中国协和医科大学肿瘤研究所肿瘤医院放射治疗科,北京100021
出 处:《肿瘤防治研究》2005年第2期116-118,共3页Cancer Research on Prevention and Treatment
摘 要:目的 通过局部晚期非小细胞肺癌放射治疗合并盐酸拓普替康(TPT)的综合治疗,进行Ⅰ期临床研究 ,观察其毒性、耐受剂量及临床可行性。方法 局部晚期肺癌 16 例,病理或细胞学证实为非小细胞肺癌。放射治疗肺部原发灶及淋巴引流区。化疗(TPT):放射治疗开始应用拓普替康,每周 2 次。每个剂量水平治疗4个星期。拓普替康分3个剂量级,0.5mg/m2,0.75mg/m2,1 mg/m2,每个剂量级至少入选3个病人,如无明显毒副反应进入下一个剂量水平,直至找到最大耐受量(MTD)。结果 主要毒副反应为骨髓抑制和放射性食管炎。MTD为0.75mg/m2。结论 局部晚期非小细胞肺癌合并 TPT综合治疗具有临床可行性,最大耐受剂量0.75mg/m2,推荐 II 期临床剂量为0.5mg/m2。Objective The current study was designed to determine the dose-limiting toxicities and clinical practicable of radiotherapy with Topotecan for local advanced non-small cell lung cancer. Methods Sixteen patients with histologically confirmed diagnosis of local late-stage NSCLC,radiotherapy include primary tumor site of lung and the area of lymph node.Patients were treated with Topotecan at three dose level ((0.5)mg/m^(2),(0.75)mg/m^(2 )and 1mg/m^(2))while the radiotherapy started. Topotecan was given intravenously twice a week over total four weeks . Dose escalation was based ,on each level ,of a minimum of three patients in cohort if severe toxicity had not been observed until the maximum tolerance dose(MTD). Results The predominant form of toxicity is hematologic toxicity and radiation esophagitis. The MTD was 0.75mg/m^(2). Conclusion Combined radiotherapy and Topotecan for treatment of local late-stage NSCLC is well tolerant. We recommend that the dose for phase II clinical trial is 0.5mg/m^(2).
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