江杭,金风,吴伟莉,李媛媛,龙金华,龚修云,陈潇潇,甘家应,李卓玲.调强放疗联合时辰化疗治疗局部进展期鼻咽癌的近期疗效及不良反应[J].中华放射医学与防护杂志,2019,39(11):813-819
调强放疗联合时辰化疗治疗局部进展期鼻咽癌的近期疗效及不良反应
Short-term efficacy and adverse events of intensity-modulated radiotherapy combined with chronomodulated chemotherapy for locally advanced nasopharyngeal carcinoma
投稿时间:2019-05-27  
DOI:10.3760/cma.j.issn.0254-5098.2019.11.003
中文关键词:  鼻咽癌  时辰化疗  调强放射治疗  不良反应  近期疗效
英文关键词:Nasopharyngeal carcinoma  Chronomodulated chemotherapy  Intensity-modulated radiotherapy  Adverse events  Short-term efficacy
基金项目:贵州省科技厅社发攻关项目黔科合SY字〔2015〕3049
作者单位E-mail
江杭 贵州医科大学附属医院肿瘤科, 贵阳 550001  
金风 贵州医科大学附属医院肿瘤科, 贵阳 550001 jinf8865@yeah.net 
吴伟莉 贵州医科大学附属医院肿瘤科, 贵阳 550001  
李媛媛 贵州医科大学附属医院肿瘤科, 贵阳 550001  
龙金华 贵州医科大学附属医院肿瘤科, 贵阳 550001  
龚修云 贵州医科大学附属肿瘤医院/贵州省肿瘤医院头颈肿瘤科, 贵阳 550004  
陈潇潇 贵州医科大学附属医院肿瘤科, 贵阳 550001  
甘家应 贵州医科大学附属医院肿瘤科, 贵阳 550001  
李卓玲 贵州医科大学附属医院肿瘤科, 贵阳 550001  
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中文摘要:
      目的 比较时辰化疗与常规化疗联合调强放疗在局部进展期鼻咽癌患者治疗过程中的不良反应、免疫功能、近期疗效。方法 选取2015年7月至2017年4月在贵州医科大学附属肿瘤医院初治局部进展期鼻咽癌患者159例,采用简单随机分组法,前瞻性将159例初治局部进展期鼻咽癌患者随机分为时辰化疗组与常规化疗组,前者采用时辰化疗模式给药,后者采用常规模式给药,两组均采用调强放射治疗,评价近期疗效及观察不良反应。结果 时辰化疗组与常规化疗组近期疗效完全缓解(CR)、部分缓解(PR)、稳定(SD)、进展(PD)差异无统计学意义(P>0.05),两组有效率(CR+PR)差异无统计学意义(P>0.05);时辰化疗组的白细胞减少(Z=-2.222,P<0.05)、中性粒细胞减少(Z=-1.999,P<0.05)、呕吐(Z=-2.298,P<0.05)、口腔黏膜炎(Z=-3.571,P<0.05)发生率低于常规化疗组,差异有统计学意义;时辰化疗组CD16+56+淋巴细胞计数高于常规化疗组(Z=-2.332,P<0.05)。结论 时辰化疗作为一种新的治疗模式,与调强放疗联合可在不降低临床疗效的同时减轻治疗相关不良反应的发生率及严重程度,减轻免疫抑制,值得临床推广及应用。
英文摘要:
      Objective To compare the adverse events, immune status, and short-term efficacy between chronomodulated chemotherapy (CCR) and routine chemotherapy (RCR) combined with intensity modulated radiotherapy (IMRT)in the treatment of patients with locally advanced nasopharyngeal carcinoma. Methods A total of 159 patients with newly diagnosed locally advanced nasopharyngeal carcinoma were randomized into the CCR group and the RCR group to evaluate the short-term efficacy and adverse events. Results No significant difference was found in CR, PR,SD, and PD between the CCR group and the RCR group (P>0.05), and no significant difference was observed in the response rate (CR+PR) between the two groups (P>0.05). The incidence of leukopenia(Z=-2.222, P<0.05), neutropenia(Z=-1.999,P<0.05), vomiting(Z=-2.298, P<0.05), and oral mucositis(Z=-3.571, P<0.05)of the CCR group was lower than those of the RCR group with statistical significance. The CD16+56+ lymphocyte cell count was higher in the CCR group than that in the RCR group(Z=-2.332,P<0.05). Conclusions As a novel invention, CCR combined with IMRT can reduce the incidence and severity of treatment-related adverse events and improve immune status without diminishing clinical efficacy, therefore deserving clinical application.
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