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三维适形放疗同步奥沙利铂化疗治疗不可手术Ⅲ期非小细胞肺癌的临床研究 被引量:5

Research of three-dimensional conformal radiotherapy combined with concurrent weekly oxaliplatin for inoperable stage Ⅲ non-small cell lung cancer
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摘要 目的 探讨三维适形放疗同步每周小剂量奥沙利铂化疗治疗不可手术Ⅲ期非小细胞肺癌(NSCLC)的疗效、毒副反应以及生存期.方法 将64例不可手术的Ⅲ期NSCLC患者分为诱导化疗后胸部三维适形放疗(3D-CRT)同步小剂量奥沙利铂化疗组(同步组)32例和诱导化疗后胸部三维适形放疗组(序贯组)32例.两组均采用以铂类为基础的化疗方案先诱导化疗2周期,获疾病控制者(CR+PR+SD)休息3~4周开始胸部三维适形放疗,同步组在放疗的同期给予小剂量奥沙利铂(50mg/次)化疗,每周1次,直至放疗结束.两组胸部放疗总剂量相同均为66Gy/33f,每周一至周五.两组放疗结束后获疾病控制者休息4~6周后进一步行多西他赛或吉西他滨单药巩固化疗2周期.结果 中位随访13.5个月,同步组和序贯组的中位总生存期(OS)分别为17.0个月和14.5个月,中位无进展生存期(PFS)分别为12.9个月和9.2个月,1年和2年生存率分别为62.5%、56.3%和28.1%、21.9%,1年和2年无进展生存率分别为40.6%、31.3%和15.6%、12.5%.毒副反应同步组的2~3级放射性食管炎发生率高(P<0.05),其他治疗相关毒性两组比较无统计学差异(P>0.05).结论 诱导化疗后胸部3D-CRT同步每周小剂量奥沙利铂化疗治疗不可手术Ⅲ期NSCLC安全有效,毒性反应轻,患者耐受性好. Objective To evaluate the toxicity and efficacy of three-dimensional conformal radiotherapy (3D-CRT) combined with oxaliplatin on inoperable stage m non-small cell lung cancer(NSCLC) patients. Methods Sixty-four inoperable NSCLC patients were divided into induction chemotherapy followed by concurrent weekly low-dose oxaliplatin and radiotherapy group (group A) or sequential chemoradiotherapy group (group B). The group A were treated with inductive cisplatin (70mg/m^2 dj-d3 ) basement chemotherapy (combined with vinorelbine 25mg/m^2 d1 ,ds or pacilitaxel 175mg/m^2 d1 or gemeitabine 1000mg/m^2 d1,d8 or docetaxel 75mg/ m^2 d1 ) for two cycles(21 days was a cycle) and followed by concurrent chemoradiotherapy ( oxaliplatin 50mg weekly for 7 weeks). The following consolidation chemotherapy was consisted of two cycles of docetaxel (75mg/m^2 d1 ) or gemeitabine (1000mg/m^2 d1 ). The group B were treated with the same inductive chemotherapy for two cycles (42 days) ; the following procedures of the therapy were same also with group A except oxaliplatin. All patients were received with the same radiotherapy (66 Gy at 2Gy per fraction, five fractions per week in both two groups). The patients were followed-up on one month, three months. Results The median follow-up time was 13.5 months (range 2-39 months). The median overall survival (OS) time was 17.0 months in group A and 14. 5 months in group B. The progression free survival (PFS) time was 12. 9 months in group A and 9. 2 months in group B. The 1- , 2-year overall survival rates were 62. 5% , 56. 3% and 28.1% , 21.9% , respectively. The 1- and 2-year progression free survival (PFS) rates were 40. 6% , 31.3% and 15.6%, 12. 5%, respectively. The major treatment related toxicities included radiation-lnduced esophagitis, radiation pneumonitis, and haematological toxicities. None of them were observed grade 4 either radiation-induced pneumonitis or esophagitis. The incidence rate of grade 3 to 4 neutropenia was 28% (group A) and 15.6% (group B) respectively (P 〉 0. 05 ). The rate of grade 2 to 3 esophagitis was 37.5% and 12. 5%, respectively (P 〈 0. 05). There was no death due to the treatment. Conclusion It is safe and efficient that the combination treatment of schedule of 3D-CRT combined with concurrent weekly low-dose oxaliplatin for inoperable stage H1 NSCLC patient,and the therapeutic effects is tended to be superior to sequential demonstration.
出处 《临床肿瘤学杂志》 CAS 2010年第11期991-995,共5页 Chinese Clinical Oncology
基金 江西省卫生厅科技计划基金项目(040328)
关键词 非小细胞肺癌 奥沙利铂 同步放化疗 Non-small cell lung cancer Oxaliplatin Concurrent chemoradiotherapy
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参考文献12

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