中华器官移植杂志
中華器官移植雜誌
중화기관이식잡지
CHINESE JOURNAL OF ORGAN TRANSPLANTATION
2009年
3期
175-178
,共4页
李秋柏%游泳%陈智超%黎纬明%夏凌辉%邹萍
李鞦柏%遊泳%陳智超%黎緯明%夏凌輝%鄒萍
리추백%유영%진지초%려위명%하릉휘%추평
白血病%造血干细胞移植%复发%抗肿瘤联合化疗方案
白血病%造血榦細胞移植%複髮%抗腫瘤聯閤化療方案
백혈병%조혈간세포이식%복발%항종류연합화료방안
Leukemia%Hematopoietic stem cell transplantation%Recurrence%Antineoplastic combined chemotherapy protocols
目的 观察氟达拉滨联合阿糖胞苷(FA方案)大剂量化疗对异基因造血干细胞移植(allo-HSCT)后急性白血病复发的治疗效果.方法 急性白血病患者10例,7例接受亲缘供者造血干细胞移植,3例接受非亲缘供者造血干细胞移植,所有患者移植后均获得造血重建,为完全供者型.10例于首次移植后38~213 d(中位数为126 d)急性白血病复发,其中完全供者型复发1例,完全受者型复发4例,混合嵌合体型复发5例.原发病复发后均采用FA方案化疗,氟达拉滨用量为25 mg/m2,阿糖胞苷用量为1.5 g/m2,用5 d,其中6例于化疗结束后第2天还接受原供者外周造血干细胞(PBSC)移植,未使用预防移植物抗宿主病(GVHD)的药物.结果 除1例早期(8 d)死亡外,其余9例再次获得造血重建,经外周血DNA序列分析证实为完全供者型.获得造血重建的9例,4例由于复发、感染、多脏器功能衰竭等原因死亡,5例无病存活至随访结束,存活时间分别为585、442、405、213和243 d.治疗后,3例未发生GVHD,其余7例发生急性或慢性GVHD;7例并发肺部真菌感染,3例并发出血性膀胱炎,4例并发巨细胞病毒血症.10例的6个月实际无病存活率为60%,2年预期无病存活率为53%.结论 对于allo-HSCT后的急性白血病复发,采用FA方案化疗,如条件允许联合原供者造血干细胞输注,可能是目前可采取的一种有效治疗方案.
目的 觀察氟達拉濱聯閤阿糖胞苷(FA方案)大劑量化療對異基因造血榦細胞移植(allo-HSCT)後急性白血病複髮的治療效果.方法 急性白血病患者10例,7例接受親緣供者造血榦細胞移植,3例接受非親緣供者造血榦細胞移植,所有患者移植後均穫得造血重建,為完全供者型.10例于首次移植後38~213 d(中位數為126 d)急性白血病複髮,其中完全供者型複髮1例,完全受者型複髮4例,混閤嵌閤體型複髮5例.原髮病複髮後均採用FA方案化療,氟達拉濱用量為25 mg/m2,阿糖胞苷用量為1.5 g/m2,用5 d,其中6例于化療結束後第2天還接受原供者外週造血榦細胞(PBSC)移植,未使用預防移植物抗宿主病(GVHD)的藥物.結果 除1例早期(8 d)死亡外,其餘9例再次穫得造血重建,經外週血DNA序列分析證實為完全供者型.穫得造血重建的9例,4例由于複髮、感染、多髒器功能衰竭等原因死亡,5例無病存活至隨訪結束,存活時間分彆為585、442、405、213和243 d.治療後,3例未髮生GVHD,其餘7例髮生急性或慢性GVHD;7例併髮肺部真菌感染,3例併髮齣血性膀胱炎,4例併髮巨細胞病毒血癥.10例的6箇月實際無病存活率為60%,2年預期無病存活率為53%.結論 對于allo-HSCT後的急性白血病複髮,採用FA方案化療,如條件允許聯閤原供者造血榦細胞輸註,可能是目前可採取的一種有效治療方案.
목적 관찰불체랍빈연합아당포감(FA방안)대제양화료대이기인조혈간세포이식(allo-HSCT)후급성백혈병복발적치료효과.방법 급성백혈병환자10례,7례접수친연공자조혈간세포이식,3례접수비친연공자조혈간세포이식,소유환자이식후균획득조혈중건,위완전공자형.10례우수차이식후38~213 d(중위수위126 d)급성백혈병복발,기중완전공자형복발1례,완전수자형복발4례,혼합감합체형복발5례.원발병복발후균채용FA방안화료,불체랍빈용량위25 mg/m2,아당포감용량위1.5 g/m2,용5 d,기중6례우화료결속후제2천환접수원공자외주조혈간세포(PBSC)이식,미사용예방이식물항숙주병(GVHD)적약물.결과 제1례조기(8 d)사망외,기여9례재차획득조혈중건,경외주혈DNA서렬분석증실위완전공자형.획득조혈중건적9례,4례유우복발、감염、다장기공능쇠갈등원인사망,5례무병존활지수방결속,존활시간분별위585、442、405、213화243 d.치료후,3례미발생GVHD,기여7례발생급성혹만성GVHD;7례병발폐부진균감염,3례병발출혈성방광염,4례병발거세포병독혈증.10례적6개월실제무병존활솔위60%,2년예기무병존활솔위53%.결론 대우allo-HSCT후적급성백혈병복발,채용FA방안화료,여조건윤허연합원공자조혈간세포수주,가능시목전가채취적일충유효치료방안.
Objective To investigate the clinical efficacy of fludarabine combined with cytarabine (FA) in treating the relapse of acute leukemia after allogeneic stem cell transplantation (allo-HSCT). Methods Ten patients with relapse of acute leukemia after allo-HSCT were retrospectively analyzed. Among the patients, PBSCs were from 7 related donors and 3 unrelated donors. After the transplantation, the median relapse time was 126 days (range,38~213 days). Two days after the FA chemotherapy, 6 patients received infusion of the same donor's peripheral blood stem cells, and the median number of CD34+ cells was 3.5×106/kg[(1.8~4.2)×106)], mobilized by granulocyte colony stimulating factor. No prophylactic agents for graft versus host diseases were administered. Results One patient who had received FA treatment and the donor's stem cell transfusion failed to acquire hematopioetic reconstitution and died 8 days after the PBSC transfusion, and the remaining 9 patients successfully got hematopioetic reconstitution of full donor chimera. Bone marrow hematological complete remission and full donor chimera were verified 30 days after the treatment in the 9 cases. Of the total 10 patients,graft versus host disease occurred in 7,and 2 of them received no donor's stem cell infusion (DSI). Seven patients suffered from pulmonary funsal infection, 3 from haemorrhagic cystitis, and 2 from cytomegalovirus viraemia. Five patients died and 5 survived with DFS till to the follow-up endpoint. The survival time for the 5 patients with DFS was 585,442, 405,213 and 243 days, respectively. The 6-month DFS rate was 60 % and the estimated 2-year DFS rate was 53 %. Conclusion FA chemotherapy, combined with reinfusion of donor's PBSC if possible, could serve as an possible effective therapeutic method for leukemia relapse after allo-HSCT.