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维生素C联合同步放化疗治疗Ⅲ期非小细胞肺癌的临床疗效 被引量:1

Clinical efficacy of vitamin C combined with concurrent chemoradiotherapy in treatment of stage III non-small cell lung cancer
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摘要 目的探究维生素C联合同步放化疗(CCRT)对Ⅲ期非小细胞肺癌(NSCLC)患者近期疗效、生存质量及免疫球蛋白(IgA、IgM、IgG)和炎症因子水平的影响。方法将2019年3月—2021年3月贵州省黔西南布依族苗族自治州人民医院收治的60例Ⅲ期NSCLC患者随机分为对照组(n=30)与试验组(n=30)。对照组患者采用CCRT治疗。放疗方案:6MV-X直线加速器扫描,每次1.8~2.0 Gy,每周5次,总剂量60~66 Gy。化疗方案:顺铂(50 mg·m^(−2))第1天(d1)、d8、d29、d36静脉滴注,依托泊苷(50 mg·m^(−2))d1~d5、d29~d33静脉滴注。36 d为1个疗程,共治疗1个疗程。试验组患者采用维生素C联合CCRT治疗,CRRT方案同对照组,CCRT治疗方案开始后即给予静脉输注维生素C,每天10 g,每周2次(间隔3 d)至放化疗结束,放化疗全程口服维生素C,每天4 g,连续治疗36 d。观察两组患者治疗后近期疗效、生存质量(KPS评分)以及血清肿瘤坏死因子-α(TNF-α)、IgA、C反应蛋白(CRP)、IgM、白细胞介素6(IL-6)、IgG水平。结果试验组客观缓解率为53.33%,略高于对照组的46.67%,但差异无显著性(P>0.05)。试验组化疗后生存质量稳定改善率83.33%显著高于对照组56.67%(P<0.05)。试验组总不良反应发生率33.33%,显著低于对照组的60.00%(P<0.05)。治疗前,两组的IgA、IgG、IgM和IL-6、CRP、TNF-α水平比较,差异无统计学意义(P>0.05);治疗后,两组IgA、IgG、IgM水平均较本组治疗前显著升高(P<0.05),IL-6、CRP、TNF-α水平较本组治疗前降低(P<0.05);与对照组治疗后比较,试验组IgA、IgG、IgM水平显著升高(P<0.05),IL-6、CRP、TNF-α水平降低(P<0.05)。结论维生素C联合CCRT治疗Ⅲ期NSCLC可显著降低不良反应发生率,改善生存质量及机体免疫功能。 Objective To investigate the influences of vitamin C combined with concurrent chemoradiotherapy(CCRT)on the shortterm response rate,quality of life and immunoglobulin(IgA,IgM,IgG)andinflammatory factor levels in patients with stage III nonsmall cell lung cancer(NSCLC).Methods Sixty patients with stage III NSCLC who were treated in People's Hospital of Qianxinan Buyei and Miao Autonomous Prefecture from March 2019 to March 2021 were randomly grouped into control group(n=30)and experimental group(n=30).Control group was treated with CCRT.Radiotherapy regimen:6MV-X linear accelerator scanning,1.8—2.0 Gy each time,five times a week,total dose 60—66 Gy.Chemotherapy regimen:Cisplatin(50 mg·m^(−2))(d1),d8,d29,d36 intravenous infusion,etoposide(50 mg·m^(−2))d1—d5,d29—d33 intravenous infusion.A total of 36 days of treatment,36 days as a course of treatment.The experimental group was treated with vitamin C combined with CCRT,and the CCRT scheme was the same as that of the control group.After the beginning of the CCRT treatment,the patients were given intravenous infusion of vitamin C,10 g a day,twice a week(3 d interval),until the end of radiotherapy and chemotherapy.During the whole course of radiotherapy and chemotherapy,oral vitamin C,4 g a day,was continuously treated for 36 d.The short-term effective rate,quality of life(KPS score),and the levels of serum tumor necrosis factor-α(TNF-α),IgA,C-reactive protein(CRP),IgM,interleukin-6(IL-6)and IgG in two groups after treatment were observed.Results The short-term effective rate of experimental group was 53.33%,slightly higher than that of control group 46.67%,but the difference was not significant(P>0.05).The stable improvement rate of quality of life after chemotherapy in experimental group was 83.33%,which was obviously higher than 56.67%in control group(P<0.05).The incidence of total adverse reactions in the experimental group was 33.33%,which was obviously lower than that in control group(60.00%)(P<0.05).Before treatment,there were no significant differences in the levels of IgA,IgG,IgM,IL-6,CRP and TNF-αbetween the two groups(P>0.05).After treatment,the levels of IgA,IgG and IgM in two groups were significantly increased compared with before treatment(P<0.05),while the levels of IL-6,CRP and TNF-αwere decreased compared with before treatment(P<0.05).Compared with the control group after treatment,the levels of IgA,IgG and IgM in experimental groups were significantly increased(P<0.05),while the levels of IL-6,CRP and TNF-αwere decreased(P<0.05).Conclusion Vitamin C combined with CCRT in the treatment of stage III NSCLC can significantly reduce adverse reactions,and improve the quality of life and immune function.
作者 袁越 胡立立 杨莉平 王万志 YUAN Yue;HU Lili;YANG Liping;WANG Wanzhi(Department of Oncology,People's Hospital of Qianxinan Buyei and Miao Autonomous Prefecture,Xingyi 562400,China)
出处 《药物评价研究》 CAS 2023年第4期829-834,共6页 Drug Evaluation Research
基金 黔西南州科技计划项目(2018-2-36)。
关键词 维生素C 非小细胞肺癌 同步放化疗 Ⅲ期 免疫功能 不良反应 vitamin C non-small cell lung cancer concurrent chemoradiotherapy stage III immune function adverse reactions
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