Effect of ATG combined cyclosporine treatment in 35 patients with severe aplastic anemia
-
摘要: 目的:分析重型再生障碍性贫血(SAA)患者进行抗胸腺细胞球蛋白(ATG)联合环孢素免疫抑制治疗的疗效。方法:回顾性分析ATG联合环孢素治疗35例SAA患者的临床资料,并随访6~88个月,分析联合免疫抑制治疗的疗效及可能的影响因素。结果:使用联合免疫抑制方案治疗SAA的总体有效率为68.6%。对免疫抑制治疗有效的患者,白细胞恢复中位时间为27(12~43) d。获得治愈的8例患者,血小板恢复时间为2~6个月,其余患者血小板未能恢复,其中有7例缓解患者不依赖血小板输注。单因素分析显示,治疗前网织红细胞计数(Ret)高于24×109/L的患者治疗有效率达88.9%,高于Ret<24×109/L的患者(61.5%)(P<0.01);+30 d时中性粒细胞绝对值(ANC)≥1.5×109/L的患者有效率为81.0%,高于ANC<1.5×109/L的患者(53.8%)(P<0.05);SAA患者的有效率为81.0%,优于极重型再障患者的50.0%(P<0.05)。结论:ATG联合环孢素治疗SAA可有效减少输血依赖,治疗前患者Ret、再障的严重程度分型、+30 d的ANC可能是预测免疫抑制治疗的疗效指标。Abstract: Objective: To analyze the effect of the ATG combined cyclosporine (CsA) in patients with severe aplastic anemia (SAA).Method: Clinical data of 35 patients with SAA receiving ATG/CsA treatment were retrospectively analyzed.After follow-up of 6 to 88 months,the efficacy of immunosuppressive therapy (IST) and the factors that may affect the efficacy were analyzed.Result: The overall effective rate was 68.6%.In patients effective to IST,the median recovery time of white blood cell was 27 (12 to 43) days.The platelet recovery time in the 8 cured patients was 2 to 6 months,and the platelet count in the remaining patients failed to rise,of which 7 relieved cases didn't depend on platelet transfusion.The patients with reticulocte count (Ret)≥24×109/L before treatment had the response rate of 88.9%,which was higher than that with Ret<24×109/L (P<0.01).The patients with the neutrophils counts (ANC)≥1.5×109/L at +30 day had a higher response rate of 81.0%,which was higher than that with ANC<1.5×109/L (P<0.05).SAA patients' response rate (81.0%) was higher than that of the VSAA (50.0%),P<0.05.Conclusion: ATG combined with CsA can effectively reduce transfusion dependence on SAA patients.The Ret count,severity of aplastic anemia and the ANC count at +30 day may predict the efficacy of IST treatment.
-
Key words:
- aplastic anemia /
- immunosuppressive therapy /
- effect analysis
-
-
[1] 张之南,沈悌.血液病诊断及疗效标准[M].3版.北京:科学出版社,2007:19-23.
[2] YOUNG N S,BACIGALUPO A,MARSH J C.Aplastic anemia:pathophysiology and treatment[J].Biol Blood Marrow Transplant,2010,16:S119-S125.
[3] TICHELLI A,SCHREZENMEIER H,SOCIE G,et al.A randomized controlled study in patients with newly diagnosed severe aplastic anemia receiving antithymocyte globulin (ATG),cyclosporine,with or without G-CSF:a study of the SAA Working Party of the European Group for Blood and Marrow Transplantation[J].Blood,2011,117:4434-4441.
[4] SCHEINBERG P,WU C O,NUNEZ O,et al.Predicting response to immunosuppressive therapy and survival in severe aplastic anaemia[J].Br J Haematol,2009,144:206-216.
[5] MATSUDA A,MISUMI M,SHIMADA T,et al.Soluble transferrin receptor and its ratio to erythroblasts in bone marrow may be a new diagnostic tool to distinguish between aplastic and refractory anemia[J].Acta Haematol,2004,111:138-142.
[6] FENG X,KAJIGAYA S,SOLOMOU E E,et al.Rabbit ATG but not horse ATG promotes expansion of functional CD4+CD25 high FOXP3+ regulatory T cells in vitro[J].Blood,2008,11:3675-3683.
[7] ATTA E H,DIAS D S,MARRA V L,et al.Comparison between horse and rabbit antithymocyte globulin as first-line treatment for patients with severe aplastic anemia:a single-center retrospective study[J].Ann Hematol,2010,89:851-859.
[8] SCHEINBERG P,NUNEZ O,Weinstein B,et al.Horse versus rabbit antithymocyte globulin in acquired aplastic anemia[J].N Engl J Med,2011,365:430-438.
[9] BING H,SIYI Y,WEI Z,et al.The use of anti-human T lymphocyte porcine immunoglobulin and cyclosporine a to treat patients with acquired severe aplastic anemia[J].Acta Haematol,2010,124:245-250.
[10] MARSH J,SOCIE G,TICHELLI A,et al.Should irradiated blood products be given routinely to all patients with aplastic anaemia undergoing immunosuppressive therapy with antithymocyte globulin (ATG)?[J].Br J Haematol,2010,150:377-379.
[11] CALADO R T,YOUNG N S.Telomere maintenance and human bone marrow failure[J].Blood,2008,111:4446-4455.
[12] CALADO R T,YEWDELL W T,WILKERSON K L,et al.Sex hormones,acting on the TERT gene,increase telomerase activity in human primary hematopoietic cells[J].Blood,2009,114:2236-2243.
[13] LOCASCIULLI A,BACIGALUPO A,BRUNO B,et al.Hepatitis-associated aplastic anaemia:epidemiology and treatment results obtained in Europe.A report of The EBMT aplastic anaemia working party[J].Br J Haematol,2010,149:890-895.
-
计量
- 文章访问数: 99
- PDF下载数: 126
- 施引文献: 0