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作 者:谢松喜[1] 李伟雄[1] 张红丹[1] 陈应瑞[1]
机构地区:[1]广东省人民医院肿瘤中心放疗科,广东广州510080
出 处:《中华肿瘤防治杂志》2009年第6期454-456,共3页Chinese Journal of Cancer Prevention and Treatment
摘 要:目的:为了探讨局部晚期鼻咽癌吉西他滨同步放化疗的毒性和疗效。方法:确定吉西他滨的最佳使用剂量,选择病理确诊的局部晚期鼻咽癌患者60例,包括T3、T4和N2、N3患者。吉西他滨分为100、50和30mg/m23个剂量,每个剂量级别至少3例患者进入研究。每周一进行吉西他滨同步放化疗,化疗结束后至少4h行放疗,同步化疗共6次,放射治疗5次/周,2Gy/次,鼻咽部总剂量70~72Gy,颈淋巴结转移灶70Gy。结果:100mg/m2剂量级别入组15例患者,4级放射性口腔黏膜炎发生率53.3%(8/15),3级放射性皮炎33.3%(5/15);50mg/m2剂量级别25例患者,4级放射性口腔黏膜炎12%(3/25),3级放射性口腔黏膜炎40%(10/25);30mg/m2剂量级别20例患者,3级放射性口腔黏膜炎40%(8/20)。60例患者中完全缓解率41.7%(25/60),部分缓解率50.0%(30/60),稳定8.3%(5/60)。1年局部控制率100%。结论:局部晚期鼻咽癌采用吉西他滨同步放化疗的最大耐受剂量为100mg/m2,推荐最佳剂量为50mg/m2,主要的毒性为放射性口腔黏膜炎和放射性皮炎,近期疗效令人鼓舞。OBJECTIVE:To preliminarily assess the efficacy and toxicity of concurrent radiotherapy and weekly gemcitabine for locally advanced nasopharyngeal carcinoma and to confirm the optimum dose of gemcitabine. METHODS: Sixty patients with nasopharyngeal carcinoma of stage Ⅲ and ⅣA including T3,T4 and N2,N3 were enrolled. Gemcitabine doses were divided to three dose levels: 100 mg/m^2, 50 mg/m^2 and 30 mg/m^2, respectively, and at least 3 patients were enrolled in each cohort. Gemcitabine was administrated intravenously over 30 minutes once weekly, and at least 4 hours before radiation for 6 weekly cycles. The nasopharyngeal region received 70-72 Gy and neck positive lymph node regions received 70 Gy, which were delivered by a conventionally fractionated schedule (2 Gy per fraction, 5 fractions per week). Sixty patients had completed radiochemotherapy. RESULTS: In the 100 mg/m^2 dose cohort there were 8 of 15 patients (53.3%,8/15) experienced grade 4 mucositis and grade 3 dermatitis for 5 patients (33.3%,5/15); 25 patients were enrolled in the 50 mg/m^2 dose cohort, 3 patients suffered from the grade 4 mucositis and 10 patients for grade 3 mucositis (40%,10/25); 8 patienst with grade 3 mucositis were observed in the 30 mg/m^2 dose cohort of 20 patients (40%,8/20). Twenty-five patients achieved complete response (41.7%,25/60), 30 patients were classed with partial response (50.0%,30/60) and 5 patients obtained stable disease (8.3%,5/60). At a median follow-up of 26 months the 1-year locoregional progression-free was 100%. CONCLUSIONS: The maximum tolerated dose of gemcitabine concurrent with radiation for locally advanced nasopharyngeal carcinoma is 100 mg/m^2 and the optimum dose is 50 mg/m^2. The major toxicities ane radiation-induced mucositis and dermatitis, but the preliminary result is promising.
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