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作 者:张燕萍[1] 周晓慧[1] 张丽[1] 马光丽[2]
机构地区:[1]江山市中医院血液内科,浙江江山324100 [2]温州医科大学附属第六医院血液科,浙江丽水323000
出 处:《中国临床药理学杂志》2015年第12期1109-1111,共3页The Chinese Journal of Clinical Pharmacology
基 金:中医药行业科研专项基金资助项目(201107001-14)
摘 要:目的:评价利妥昔单抗联合改良CHOP方案(600 mg· m-2环磷酰胺,第1天+1.4 mg· m-2长春新碱,第1天+泼尼松60 mg,第1~5天+25 mg· m-2阿霉素,第1天)治疗复发难治性非霍奇金淋巴瘤的临床疗效及安全性。方法将62例复发难治性非霍奇金淋巴瘤患者随机分为试验组29例和对照组33例。对照组:改良 CHOP 方案联合10 mg· m-2博来霉素,第1天+75 mg· m-2足叶乙苷,第1~5天;试验组:在改良CHOP方案实施前2 d,静脉输注375 mg· m-2利妥昔单抗。2组1个周期均为21 d,共治疗4~6个周期。分析比较2组患者的临床疗效及不良反应发生率。结果试验组的客观缓解率93.10%显著高于对照组75.76%(P<0.05)。试验组平均缓解时间(14.6±3.8)个月显著长于对照组(6.4±2.2)个月(P<0.05)。2组患者不良反应发生率比较差异无统计学意义(P>0.05)。结论利妥昔单抗联合改良CHOP方案治疗复发难治性非霍奇金淋巴瘤临床的疗效确切,可显著延长患者的疾病缓解时间。Objective To assess the effects and safety of rituximab com-bined with CHOP chemotherapy regimen ( 600 mg· m-2 cytoxan on day 1+1.4 mg· m-2 vinblastine on day 1+prednisone 60 mg on day 1 to 5+25 mg· m-2 adriamycin on day 1 ) in the treatment of relapsing non-hodgkin′s lymphoma.Methods A total of 62 cases of relapsing non-hodgkin′s lymphoma were divided into experiment group ( n=29 ) and control group ( n =33 ) .Patients in the control group were given CHOP regimen combined with 10 mg· m-2 bleomycin on day 1 and 5 mg· m-2 etoposide on day 1 to 3.Patients in experiment group were given 375 mg· m-2 rituximab 2 days before CHOP chemotherapy.All of the patients underwent 4 to 6 cycles of chemotherapy (21 days was a cy-cle).The clinical effects and adverse reactions were evaluated between the two groups.Results The objective response rate were 93.10%and 75.76%in experiment and control group respectively ( P 〈0.05 ) .The mean complete response time were ( 14.6 ±3.8 ) months in experiment group, higher than(6.4 ±2.2) months in control group( P〈0.05).The main adverse reaction in two groups were not statistically different (P〉0.05).Conclusion Rituximab combined with CHOP chemothera-py regimen can improve the clinical efficacy and complete response time on patients with relapsing non-hodgkin′s lymphoma.
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