>
网站首页期刊介绍通知公告编 委 会投稿须知电子期刊广告合作联系我们
最新消息:
阿扎胞苷对中高危骨髓增生异常综合征的临床疗效观察
作者:姚伟  李静  刘桂玲 
单位:蚌埠市第三人民医院 血液内科, 安徽 蚌埠 233000
关键词:骨髓增生异常综合征 阿扎胞苷 地西他滨 
分类号:R733.3
出版年·卷·期(页码):2020·39·第二期(193-196)
摘要:

目的:比较单纯应用去甲基药物阿扎胞苷(AZA)和阿糖胞苷(Ara-c)加阿克拉霉素(ACR)加粒细胞集落刺激因子(G-CSF)的CAG方案联合地西他滨对中高危骨髓增生异常综合征(MDS)的疗效和安全性。方法:回顾性分析我院50例中高危MDS患者的临床资料,其中20例患者采用CAG联合地西他滨方案,30例患者单用AZA,比较治疗4个疗程后两组患者对治疗的反应率及不良反应发生率的差异。结果:治疗4个疗程后,CAG联合地西他滨方案组治疗的总有效率(ORR)为64.7%,包括完全缓解(CR)3例、部分缓解(PR)3例、血液学改善(HI)6例,AZA组ORR为66.7%,包括CR 5例、PR 13例、HI 2例,两组ORR差异无统计学意义(P>0.05),但缓解(PR+CR)率差异具有统计学意义(P=0.04)。不良反应方面,AZA组较CAG联合地西他滨方案组Ⅲ~Ⅳ级血红蛋白减少、Ⅲ~Ⅳ级血小板减少、Ⅲ~Ⅳ级中性粒细胞绝对值减少的发生率均显著降低,两组间感染的发生率差异无统计学意义。结论:AZA治疗高危MDS较CAG联合地西他滨方案缓解率显著提高,不良反应显著减少,值得在不能进行骨髓造血干细胞移植的中高危MDS患者中推广。

Objective: To compare the efficacy and safety of demethylated drug azacitidine(AZA) with those of CAG, which consisted of cytarabine arabinoside(ara-c), acramycin(ACR) and granulocyte colony-stimulating factor(G-CSF), combined with descitabine in the treatment of patients with middle and high risk myelodysplastic syndrome(MDS). Methods: Clinical data of 50 MDS cases were retrospectively analyzed, of whom 20 cases were treated with CAG combined with descitabine and 30 received azacitidine treatment alone. The response rate and the incidence of adverse reactions between the two groups after 4 courses of treatment were compared. Results: After 4 courses of treatment, the overall response rate(ORR) of the group CAG combined with descitabine was 64.7%, including 3 complete response(CR), 3 partial response(PR) and 6 hematological improvement(HI), while the ORR in azacytarine group was 66.7%,including 5 CR, 13 PR and 2 HI. There was no statistically significant difference in ORR between the two groups(P>0.05), but there was statistically significant difference in the response rate of CR and PR(P=0.04). In terms of adverse reactions, compared to the group CAG combined with descitabine,the incidence of Ⅲ-Ⅳ level decrease in hemoglobin, platelet count and absolute neutrophil count in azacytarine group were lower. There were no statistically significant differences in the incidence of infection between the two groups. Conclusion: Compared with CAG combined with descitabine, AZA can significantly increase the remission rate and reduce the occurrence of adverse reactions in the treatment of patients with middle and high risk MDS. Therefore, it is worthy to be promoted in MDS patients who are not feasible to undergo bone marrow hematopoietic stem cell transplantation.

参考文献:

[1] NEUKIRCHEN J,SCHOONEN W M,STRUPP C,et al.Incidence and prevalence of myelodysplastic syndromes:data from the Düsseldorf MDS-registry[J].Leuk Res,2011,35(12):1591-1596.
[2] 梁亮,吴国才,聂丽容,等.减低剂量的地西他滨联合CAG方案治疗中高危骨髓增生异常综合征及难治性白血病的疗效[J].中国老年学杂志,2015,35(8):2073-2075.
[3] MUSTO P,MAURILLO L,SPAGNOLI A,et al.Azacitidine for the treatment of lower risk myelodysplastic syndromes:a retrospective study of 74 patients enrolled in an Italian named patient program[J].Cancer,2010,116(6):1485-1494.
[4] SILVERMAN L R,DEMAKOS E P,PETERSON B L,et al.Randomized controlled trial of azacitidine in patients with the myelodysplastic syndrome:a study of the cancer and leukemia group B[J].J Clin Oncol,2002,20(10):2429-2440.
[5] FENAUX P,MUFTI G J,HELLSTROM-LINDBERG E,et al.Efficacy of azacitidine compared with that of conventional care regimens in the treatment of higher-risk myelodysplastic syndromes:a randomised,open-label,phase Ⅲ study[J].Lancet Oncol,2009,10(3):223-232.
[6] PLEYER L,BURGSTALLER S,STAUDER R,et al.Azacitidine front-line in 339 patients with myelodysplastic syndromes and acute myeloid leukaemia:comparison of French-American-British and World Health Organization classifications[J].J Hematol Oncol,2016,9(1):39-54.
[7] SEKERES M A,OTHUS M,LIST A F,et al.Randomized phase Ⅱ study of azacitidine alone or in combination with lenalidomide or with vorinostat in higher-risk myelodysplastic syndromes and chronic myelomonocytic leukemia:North American Intergroup Study SWOG S1117[J].J Clin Oncol,2017,35(24):2745-2753.
[8] CHESON B D,GREENBERG P L,BENNETT J M,et al.Clinical application and proposal for modification of the International Working Group(IWG) response criteria in myelodysplasia[J].Blood,2006,108(2):419-425.
[9] GREENBERG P L,STONE R M,AL-KALI A,et al.Myelo-dysplastic syndromes,version 2.2017,NCCN clinical practice guidelines in oncology[J].J Natl Compr Canc Netw,2017,15(1):60-87.
[10] FLOTHO C,CLAUS R,BATZ C,SCHNEIDER M,et al.The DNA methyltransferase inhibitors azacitidine,decitabine and zebularine exert differential effects on cancer gene expression in acute myeloid leukemia cells[J].Leukemia,2009,23(2):1019-1028.
[11] TSUJIOKA T,YOKOI A,UESUGI M,et al.Effects of DNA methyltransferase inhibitors(DNMTIs) on MDS-derived cell lines[J].Exp Hematol,2013,41(2):189-197.

服务与反馈:
文章下载】【发表评论】【查看评论】【加入收藏
提示:您还未登录,请登录!点此登录
您是第 418304 位访问者


copyright ©《东南大学学报(医学版)》编辑部
联系电话:025-83272481 83272483
电子邮件:
bjb@pub.seu.edu.cn

苏ICP备09058364