中国临床新医学
中國臨床新醫學
중국림상신의학
CHINESE JOURNAL OF NEW CLINICAL MEDICINE
2013年
9期
836-839
,共4页
黎宇苗%毛平%王顺清%李庆山%张玉平%陈小卫%周铭%王彩霞
黎宇苗%毛平%王順清%李慶山%張玉平%陳小衛%週銘%王綵霞
려우묘%모평%왕순청%리경산%장옥평%진소위%주명%왕채하
造血干细胞移植%急性单核细胞白血病%疗效
造血榦細胞移植%急性單覈細胞白血病%療效
조혈간세포이식%급성단핵세포백혈병%료효
Hematopoietic stem cell transplantation%Acute monocytic leukemia%Efficacy
目的评价异基因外周血造血干细胞移植(allo-PBSCT)治疗急性单核细胞白血病(M5)的疗效,并探讨其并发症的预防及处理。方法16例M5患者接受allo-PBSCT,其中亲缘11例,非亲缘5例。预处理方案:9例采用清髓方案BUCY,7例采用非清髓方案FBC。亲缘的11例均采用环孢素+短程甲氨蝶呤预防移植物抗宿主病(GVHD),非亲缘的5例均采用环孢素+甲氨蝶呤+吗替麦考酚酯+ATG。输注的外周血干细胞有核细胞中位数为6.58×108/kg,CD34+细胞中位数为4.46×106/kg。结果16例患者中15例均证实植活,余1例在移植早期因HVOD死亡。植入病人中白细胞植入中位时间为13(9~17)d,血小板>20×109/L的中位时间为16(8~26)d。发生急性GVHD 6例(Ⅰ度4例,Ⅱ度2例),发生局限性慢性GVHD 7例。目前无病存活10例,中位生存期为45(3~78)个月。结论Allo-PBSCT是治疗M5的有效手段,并发症少,能有效延长患者生存时间。
目的評價異基因外週血造血榦細胞移植(allo-PBSCT)治療急性單覈細胞白血病(M5)的療效,併探討其併髮癥的預防及處理。方法16例M5患者接受allo-PBSCT,其中親緣11例,非親緣5例。預處理方案:9例採用清髓方案BUCY,7例採用非清髓方案FBC。親緣的11例均採用環孢素+短程甲氨蝶呤預防移植物抗宿主病(GVHD),非親緣的5例均採用環孢素+甲氨蝶呤+嗎替麥攷酚酯+ATG。輸註的外週血榦細胞有覈細胞中位數為6.58×108/kg,CD34+細胞中位數為4.46×106/kg。結果16例患者中15例均證實植活,餘1例在移植早期因HVOD死亡。植入病人中白細胞植入中位時間為13(9~17)d,血小闆>20×109/L的中位時間為16(8~26)d。髮生急性GVHD 6例(Ⅰ度4例,Ⅱ度2例),髮生跼限性慢性GVHD 7例。目前無病存活10例,中位生存期為45(3~78)箇月。結論Allo-PBSCT是治療M5的有效手段,併髮癥少,能有效延長患者生存時間。
목적평개이기인외주혈조혈간세포이식(allo-PBSCT)치료급성단핵세포백혈병(M5)적료효,병탐토기병발증적예방급처리。방법16례M5환자접수allo-PBSCT,기중친연11례,비친연5례。예처리방안:9례채용청수방안BUCY,7례채용비청수방안FBC。친연적11례균채용배포소+단정갑안접령예방이식물항숙주병(GVHD),비친연적5례균채용배포소+갑안접령+마체맥고분지+ATG。수주적외주혈간세포유핵세포중위수위6.58×108/kg,CD34+세포중위수위4.46×106/kg。결과16례환자중15례균증실식활,여1례재이식조기인HVOD사망。식입병인중백세포식입중위시간위13(9~17)d,혈소판>20×109/L적중위시간위16(8~26)d。발생급성GVHD 6례(Ⅰ도4례,Ⅱ도2례),발생국한성만성GVHD 7례。목전무병존활10례,중위생존기위45(3~78)개월。결론Allo-PBSCT시치료M5적유효수단,병발증소,능유효연장환자생존시간。
Objective To study the therapeutic effectiveness and associated complications of allogeneic pe -ripheral blood stem cells transplantation (Allo-PBSCT) in treatment of acute monocytic leukemia (M5 ).Methods Sixteen patients with acute monocytic leukemia received allo-PBSCT,11 patients received PBSCT from human leuco-cyte antigen(HLA)-matched sibling donors and 5 from HLA-matched unrelated donors.Pre-Processing regimen:9 patients were subjected to modified BU/CY2 regimen which was myeloablative , another 7 patients were subjected to FBC regimen which was non-myeloablative.The graft-versus-host disease(GVHD) was prevented by cyclosporin A (CsA),short-term methotrexate(MTX)in 11 patients who received PBSCT from HLA-matched sibling donors, and another 5 patients additionally received antithymocyte globulin (ATG) and mycophenolate mofetil (MMF).A median of 6.58 ×10 8/kg nucleated cells and 4.46 ×10 6/kg CD34+cells were transfused.Results Except for 1 patient died early after transplantation because of hepatic veno-occlusie disease(HVOD).Other 15 patients achieved engraftment confirmed by blood type, chromosome test and DNA polymorphism,with median times of neutrophil >0.5 ×10 9/L and platelet >20 ×10 9/L being 13(9~17)d and 16(8~26)d respectively.Six patients developed acute GVHD (4 developed gradeⅠand 2 developed gradeⅡ).Seven patients experienced local chronic GVHD .Ten patients were found to have disease-free survival(DFS), median of 45 (3~78)months.Conclusion Allo-PBSCT was an effective therapy for acute monocytic leukemia,it was safe and feasible,and long term survival was hoped for patients of this type.