中国临床药理学杂志
中國臨床藥理學雜誌
중국림상약이학잡지
THE CHINESE JOURNAL OF CLINICAL PHARMACOLOGY
2015年
12期
1109-1111
,共3页
张燕萍%周晓慧%张丽%马光丽
張燕萍%週曉慧%張麗%馬光麗
장연평%주효혜%장려%마광려
利妥昔单抗%改良CHOP方案%非霍奇金淋巴瘤%临床疗效
利妥昔單抗%改良CHOP方案%非霍奇金淋巴瘤%臨床療效
리타석단항%개량CHOP방안%비곽기금림파류%림상료효
rituximab%CHOP regimen%non-hodgkin′s lymphoma%clinical efficacy
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。
目的:評價利妥昔單抗聯閤改良CHOP方案(600 mg? m-2環燐酰胺,第1天+1.4 mg? m-2長春新堿,第1天+潑尼鬆60 mg,第1~5天+25 mg? m-2阿黴素,第1天)治療複髮難治性非霍奇金淋巴瘤的臨床療效及安全性。方法將62例複髮難治性非霍奇金淋巴瘤患者隨機分為試驗組29例和對照組33例。對照組:改良 CHOP 方案聯閤10 mg? m-2博來黴素,第1天+75 mg? m-2足葉乙苷,第1~5天;試驗組:在改良CHOP方案實施前2 d,靜脈輸註375 mg? m-2利妥昔單抗。2組1箇週期均為21 d,共治療4~6箇週期。分析比較2組患者的臨床療效及不良反應髮生率。結果試驗組的客觀緩解率93.10%顯著高于對照組75.76%(P<0.05)。試驗組平均緩解時間(14.6±3.8)箇月顯著長于對照組(6.4±2.2)箇月(P<0.05)。2組患者不良反應髮生率比較差異無統計學意義(P>0.05)。結論利妥昔單抗聯閤改良CHOP方案治療複髮難治性非霍奇金淋巴瘤臨床的療效確切,可顯著延長患者的疾病緩解時間。
목적:평개리타석단항연합개량CHOP방안(600 mg? m-2배린선알,제1천+1.4 mg? m-2장춘신감,제1천+발니송60 mg,제1~5천+25 mg? m-2아매소,제1천)치료복발난치성비곽기금림파류적림상료효급안전성。방법장62례복발난치성비곽기금림파류환자수궤분위시험조29례화대조조33례。대조조:개량 CHOP 방안연합10 mg? m-2박래매소,제1천+75 mg? m-2족협을감,제1~5천;시험조:재개량CHOP방안실시전2 d,정맥수주375 mg? m-2리타석단항。2조1개주기균위21 d,공치료4~6개주기。분석비교2조환자적림상료효급불량반응발생솔。결과시험조적객관완해솔93.10%현저고우대조조75.76%(P<0.05)。시험조평균완해시간(14.6±3.8)개월현저장우대조조(6.4±2.2)개월(P<0.05)。2조환자불량반응발생솔비교차이무통계학의의(P>0.05)。결론리타석단항연합개량CHOP방안치료복발난치성비곽기금림파류림상적료효학절,가현저연장환자적질병완해시간。
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.