Ai H, Fu Y W, Wang Y Q, Wei X D, Song Y P
Department of Hematology, The Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou 450008, China.
Zhonghua Xue Ye Xue Za Zhi. 2019 Oct 14;40(10):827-830. doi: 10.3760/cma.j.issn.0253-2727.2019.10.006.
To investigate the safety and efficacy of allogeneic hematopoietic stem cell transplantation (allo-HSCT) containing cladribine sequential busulfan regimen for refractory/relapsed acute myeloid leukemia (AML) . The clinical data of 12 refractory/relapsed AML patients received allo-HSCT with cladribine sequential busulfan regimen. ① Of the 12 patients, 9 were males and 3 females, with a median age of 36 (27-50) years. The donors were identical sibling (3) , matched unrelated (1) and haploidentical family member (9) respectively. Nine patients reached partial remission and other remained no remission after chemotherapy before allo-HSCT. The median previous chemotherapy courses before allo-HSCT were 6 (2-13) . ② Conditioning regimen: Smostine 250 mg·m(-2)·d(-1), d-7; Cladribine 5 mg·m(-2)·d(-1), d-6 to d-2; Cytarabine Arabinoside 2 g·m(-2)·d(-1), d-6 to d-2; Busulfan 3.2 mg·m(-2)·d(-1), d-6 to d-3; Rabbit anti-human thymocyte immunoglobulin (ATG) 1.5 mg·m(-2)·d(-1) (unrelated donor transplantation) or 2.0-2.5 mg·m(-2)·d(-1) (haplo-HSCT) , d-4 to d-1. ③ Of the 12 patients, 11 patients attained complete haploidentical engraftment, one case occurred primary graft failure. The median durations for neutrophils and platelet implantations were 15 (15-21) and 19 (17-30) days respectively. ④After conditioning, no hepatic veno-occlusive diseases were observed, hemorrhagic cystitis occurred in 2 patients, 8 patients had fever, 3 cases experienced acute GVHD grade II, localized chronic GVHD occurred in 8 patients. ⑤The median follow-up was 8 (4-12) months. Leukemia relapse occurred in 2 patients at time of 6, 12 months after allo-HSCT. The estimated 1-year OS and DFS were (71.1±1.8) % and (62.2±1.8) %, respectively. allo-HSCT with cladribine sequential busulfan regimen was a feasible choice with favorable outcome for refractory/relapsed AML.
探讨含克拉屈滨序贯白消安方案的异基因造血干细胞移植(allo-HSCT)治疗难治性/复发性急性髓系白血病(AML)的安全性和疗效。回顾性分析12例接受含克拉屈滨序贯白消安方案allo-HSCT的难治性/复发性AML患者的临床资料。①12例患者中,男性9例,女性3例,中位年龄36(27 - 50)岁。供者分别为同基因同胞(3例)、人类白细胞抗原(HLA)全相合非血缘供者(1例)和单倍体相合家庭成员(9例)。allo-HSCT前9例患者化疗后达部分缓解,其余患者化疗未缓解。allo-HSCT前既往化疗疗程中位数为6(2 - 13)个。②预处理方案:司莫司汀250 mg·m(-2)·d(-1),d - 7;克拉屈滨5 mg·m(-2)·d(-1),d - 6至d - 2;阿糖胞苷2 g·m(-2)·d(-1),d - 6至d - 2;白消安3.2 mg·m(-2)·d(-1),d - 6至d - 3;兔抗人胸腺细胞免疫球蛋白(ATG)1.5 mg·m(-2)·d(-1)(非血缘供者移植)或2.0 - 2.5 mg·m(-2)·d(-1)(单倍体造血干细胞移植),d - 4至d - 1。③12例患者中,11例单倍体相合造血干细胞成功植入,1例发生原发性移植失败。中性粒细胞和血小板植入中位时间分别为15(15 - 21)天和19(17 - 30)天。④预处理后,未观察到肝静脉闭塞病,2例患者发生出血性膀胱炎,8例患者发热,3例发生急性移植物抗宿主病(GVHD)Ⅱ度,8例患者发生局限性慢性GVHD。⑤中位随访时间为8(4 - 12)个月。2例患者分别于allo-HSCT后6个月、12个月白血病复发。估计1年总生存率(OS)和无病生存率(DFS)分别为(71.1±1.8)%和(62.2±1.8)%。含克拉屈滨序贯白消安方案的allo-HSCT是治疗难治性/复发性AML的一种可行选择,疗效良好。