郭灵, 林焕新, 邱枋, 孙蕊, 罗东华, 洪明晃, 冼励坚, F. LEVY. 5-FU与DDP时间调节化疗治疗晚期鼻咽癌的初步临床观察[J]. 中国肿瘤临床, 2004, 31(13): 721-724.
引用本文: 郭灵, 林焕新, 邱枋, 孙蕊, 罗东华, 洪明晃, 冼励坚, F. LEVY. 5-FU与DDP时间调节化疗治疗晚期鼻咽癌的初步临床观察[J]. 中国肿瘤临床, 2004, 31(13): 721-724.
Guo Ling, Lin Huan-xin, Qiu Fang, . Feasibility Study of Chronomodulated Chemotherapy with 5-FU±LV and DDP in the Treatment of Advanced Nasopharyngeal Cancer[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2004, 31(13): 721-724.
Citation: Guo Ling, Lin Huan-xin, Qiu Fang, . Feasibility Study of Chronomodulated Chemotherapy with 5-FU±LV and DDP in the Treatment of Advanced Nasopharyngeal Cancer[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2004, 31(13): 721-724.

5-FU与DDP时间调节化疗治疗晚期鼻咽癌的初步临床观察

Feasibility Study of Chronomodulated Chemotherapy with 5-FU±LV and DDP in the Treatment of Advanced Nasopharyngeal Cancer

  • 摘要: 目的:探讨5-FU、DDP时间调节给药法治疗晚期鼻咽癌的不良反应及疗效。方法:2001年3月到2003年1月,中山大学肿瘤防治中心鼻咽癌科对30例经病理学证实未接受过化疗的晚期鼻咽癌患者进行时间调节化疗,其中初治局部晚期(诱导化疗组)20例,初治转移、治疗后复发和(或)转移(单纯化疗组)10例。应用Melodie多通道编程输液泵进行电脑调控的正弦曲线形式时间调节给药。诱导化疗组于第1~5天、第22~26天分别行2程诱导化疗,方案为5-FU750~850mg/m2·天;DDP20mg/m2·天,连续给药5天,5-FU由22h至第2天早10h给药,浓度高峰为凌晨4h;DDP由早10h至晚22h给药,浓度高峰为下午4h,第5周开始放疗。单纯化疗组行2~6程化疗,方案为5-FU600mg/m2·天;LV200mg/m2·天;DDP20mg/m2·天,连续给药5天,每3周重复,给药方法及达峰时间与诱导化疗组相同,其中LV与5-FU给药方法一致。结果:诱导化疗组2程化疗后有效率(PR)达100%;全疗程结束CR达95.0%(19/20)。单纯化疗组PR80.0%(8/10),病情稳定(SD)10.0%(1/10),病情进展(PD)10.0%(1/10)。两组不良反应主要为Ⅲ~Ⅳ度迟发性血小板减少,发生于26.7%(8/30)的患者、14.1%(13/92)的疗程,其余不良反应有轻微性差异。结论:晚期鼻咽癌时间调节化疗不良反应小,疗效明确,值得进行深入临床研究。

     

    Abstract: objective: To investigate the efficacy and the adverse effects of chronomodulated chemotherapy by 5-FU±LV+DDP in the treatment of advanced nasopharyngeal cancer patients. Methods: From 03/2001 to 01/2003, 30 patients with pathologically diagnosed advanced nasopharyngeal cancer who were never received chemotherapy were included, among which 20 were with locally advanced primary diseases (Induction CT group); 10 with metastatic primary diseases or recurrent and/or metastatic diseases (Induction CT group). Using "Melodie" multi-channel programmed pump made of AGUETTANT company France, the patients received a five-day course of 5-FU LY (5FU 600/m2 and LY 200mg/m2 for CT group; 5FU 750-850mg/m2 without CF for Induction CT group; peak delivery rate at 04:00) and DDP (20mg/m2, peak delivery at 16:00). Each course was repeated every 3 weeks. 2 cycles of chemotherapy were given for Induction CT group before radiotherapy and 2 to 6 cycles were given for CT group. Results: For Induction CT group, all were achieved partial response after 2 cycles of neoadjuvant chemotherapy. The complete response were 95% (19/20) after the end of radical radiotherapy. For CT group, Partial Response(PR) was 80%, Stable Disease (SD) was 20%(2/10),and Progression Disease (PD) was 10% (1/10). The main adverse effect is thrombocytopenia which was found in 26.1% of patients (8/30) and 14.1% (13/92) of cycles. Other adverse effects were mild. Conclusions: For advanced nasopharyngeal cancer patients, chronomodulated infusion of 5-FU±LV+DDP can get the treatment effects with minimal adverse effects. Further clinical research is recommended to test its contribution to survival.

     

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