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利妥昔单抗辅助CHOP方案治疗B细胞型非霍奇金淋巴瘤的可行性研究 被引量:1
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作者 张晓芸 《系统医学》 2019年第7期123-125,共3页
目的分析利妥昔单抗辅助CHOP方案治疗B细胞型非霍奇金淋巴瘤的可行性。方法以2015年1月—2017年10月进入该院治疗的52例B细胞型非霍奇金淋巴瘤患者为调查目标,结合其个人意愿划入联合组与常规组(n=26)。常规组应用CHOP方案治疗,联合组... 目的分析利妥昔单抗辅助CHOP方案治疗B细胞型非霍奇金淋巴瘤的可行性。方法以2015年1月—2017年10月进入该院治疗的52例B细胞型非霍奇金淋巴瘤患者为调查目标,结合其个人意愿划入联合组与常规组(n=26)。常规组应用CHOP方案治疗,联合组在此基础上应用利妥昔单抗治疗,对比两组患者的整体有效率、不良反应发生率及生存情况。结果联合组患者整体治疗有效率为96.15%,显著高于常规组患者整体治疗有效率76.92%,数据对比差异有统计学意义(χ~2=7.17,P=0.017<0.05)。治疗期间常规组患者出现5例不良反应,联合组患者出现4例不良反应,组间数据比较无统计学意义(χ~2=2.01,P>0.05)。随访12个月,联合组死亡2例,常规组死亡6例,差异有统计学意义(χ~2=7.41,P<0.05)。结论利妥昔单抗辅助CHOP方案治疗B细胞型非霍奇金淋巴瘤,有助于提升患者的临床治疗有效率,且联合用药方式下不会显著增加患者不良反应发生率。 展开更多
关键词 利妥昔单抗 chop方案治疗 B细胞型非霍奇金淋巴瘤
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FND与CHOP方案治疗非霍奇金淋巴瘤的疗效及安全性对比 被引量:1
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作者 陈东玉 《中国伤残医学》 2015年第7期133-134,共2页
目的:对比FND与CHOP方案治疗非霍奇金淋巴瘤的临床疗效及安全性。方法:选择我院收治经确诊非霍奇金淋巴瘤患者86例,按照随机及征询患者意见原则分为观察组和对照组各43例,观察组采取FND化疗方案,对照组采用CHOP化疗方案,对比2组... 目的:对比FND与CHOP方案治疗非霍奇金淋巴瘤的临床疗效及安全性。方法:选择我院收治经确诊非霍奇金淋巴瘤患者86例,按照随机及征询患者意见原则分为观察组和对照组各43例,观察组采取FND化疗方案,对照组采用CHOP化疗方案,对比2组疗效及不良反应。结果:观察组总有效率86.05%,显著高于对照组的55.81%,差异有统计学意义(P〈0.05);FND方案治疗的不良反应主要为骨髓抑制及恶心呕吐等,患者易耐受。CHOP方案的毒性反应主要表现为脱发及胃肠道反应等。结论:采用FND化疗方案治疗非霍奇金淋巴瘤治疗具有较高的治疗总有效率,临床效果显著,不良反应轻微易耐受,可靠安全,值得临床推广应用。 展开更多
关键词 FND chop治疗方案 非霍奇金淋巴瘤 疗效对比
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Clinical randomized comparative trial of DICE regimen and CHOP regimen in treating intermediate and high grade non-Hodgkin’s lymphoma
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作者 Wenwu Wang Xuenong OuYang Zhangshu Cheng Yonghai Peng Fangwei Xie Zongyang Yu 《The Chinese-German Journal of Clinical Oncology》 CAS 2008年第2期107-110,共4页
Objective: To compare efficacies and safeties of DICE and CHOP regimens in treating intermediate and high grade non-Hodgkin's lymphoma (NHL), and indicate the standard treatment for it. Methods: A total of 74 pati... Objective: To compare efficacies and safeties of DICE and CHOP regimens in treating intermediate and high grade non-Hodgkin's lymphoma (NHL), and indicate the standard treatment for it. Methods: A total of 74 patients with moder- ately or highly malignant NHL, verified by pathology or histology, were randomized into the trial group (37 patients treated with DICE regimen) and the control group (37 patients treated with CHOP regimen). Survival rate was analyzed by Kaplan-Meier method. Chi-square test was performed between groups. Results: The complete response rate, partial response rate, and response rate were significantly higher in DICE group than in CHOP group (40.5% vs. 29.7%, 37.8% vs. 27.0%, and 78.3% vs. 56.7%, respectively, P < 0.05). The 1-, 3-, and 5-year survival rates were significantly higher in DICE group than in CHOP group (89.2% vs. 81.2%, 76.0% vs. 52.6%%, and 46.7% vs. 36.4%, respectively, P < 0.05). The major side effects, appeared with no differences (P > 0.05) in incidences between the two groups, were leukopenia, thrombocytopenia, and nausea. There were only three episodes of clinical cystitis or gross haematuria in DICE regimen. Conclusion: The results showed higher efficacy of DICE regimen over CHOP regimen. DICE regimen may prolong the survival time of patients with moderately and highly malignant NHL. 展开更多
关键词 non-Hodgkin's lymphoma combined chemotherapy comparative trial
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