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放疗同步替莫唑胺化疗治疗恶性胶质瘤临床观察 被引量:10

Effect of radiotherapy plus concomitant and adjuvant temozolomide on malignant glioma
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摘要 目的研究术后放疗同步替莫唑胺(RT-TMZ)治疗恶性胶质瘤的近期疗效和不良反应。方法收集2008年11月-2009年5月在我院确诊的61例恶性胶质瘤术后患者,按照患者自愿选择的治疗方案分为RT-TMZ组和单纯放疗(RT)组。RT-TMZ组31例,行放疗(总剂量60Gy,共治疗6周)期间同时持续口服替莫唑胺(Temozolomide,TMZ)化疗(75mg/(m2·d),共42d),放疗结束后续行TMZ辅助化疗150-200mg/(m2·d),共4-6个周期;RT组30例,单纯放疗6周,总剂量60Gy。结果RT-TMZ组与RT组有效率(CR+PR)分别为79.3%(23/29)、53.3%(16/30),疾病控制率(CR+PR+SD)分别为89.7%(26/29)、83.3%(25/30),P<0.05。RT-TMZ组6个月无疾病进展生存率为71.0%(22/31),患者对治疗的耐受性良好;不良反应为恶心、呕吐和乏力,白细胞和血小板下降基本限于I-Ⅱ度。结论恶性胶质瘤术后放疗同步替莫唑胺治疗近期疗效良好,不良反应较轻,是切实可行的治疗方案。 Objective To study the effect of temozolomide combined with radiotherapy(RT-TMZ)on malignant glioma after operation and its toxic side effects.Methods Sixty-one patients with malignant glioma admitted to our hospital in November 2008-May 2009 were divided into RT-TMZ group(n=31)and RT group(n=30).Patients in RT-TMZ group received radiotherapy with a total dosage of 60Gy and chemotherapy with oral temozolomide(TMZ),75mg/(m^2·d)for 42 days,followed by 4-6 cycles of adjuvant TMZ,150-200mg/(m^2·d).Patients in RT group received only radiotherapy with a total dosage of 60Gy for 42 days.Results The response rate was 79.3%(23/29)and 53.3%(16/30)respectively in RT-TMZ group and RT group.The disease control rate was 89.7%(26/29)and 83.3%(25/30)respectively in the two groups.The 6-month survival rate was 71.0%(22/31)in RT-TMZ group with no disease progress.The patients had a rather good tolerance to radiotherapy and chemotherapy.The main side effects included nausea,vomiting,and anorexia.The number of white blood cells and platelets was decreased.Conclusion Radiotherapy plus concomitant and adjuvant temozolomide has a rather good short-term efficacy on malignant glioma with less side effects and is a practical treatment modality for malignant glioma.
出处 《军医进修学院学报》 CAS 2010年第6期551-552,554,共3页 Academic Journal of Pla Postgraduate Medical School
关键词 神经胶质瘤 放射疗法 替莫唑胺 Glioma Radiotherapy Temozolomide
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  • 1王忠诚主编..王忠诚神经外科学[M].武汉:湖北科学技术出版社,2005:1124.
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