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伊马替尼联合清髓性异基因造血干细胞移植治疗慢性髓性白血病晚期。

Imatinib combined with myeloablative allogeneic hematopoietic stem cell transplantation for advanced phases of chronic myeloid leukemia.

机构信息

Bone Marrow Transplant Center, The First Affiliated Hospital, School of Medicine, Zhejiang University, 79 Qingchun Road, Hangzhou, China.

出版信息

Leuk Res. 2011 Oct;35(10):1307-11. doi: 10.1016/j.leukres.2011.01.001. Epub 2011 Feb 26.

DOI:10.1016/j.leukres.2011.01.001
PMID:21354617
Abstract

To evaluat the efficacy and safety of myeloablative allogeneic hematopoietic stem cell transplantation (allo-HSCT) combined with imatinib for advanced chronic myeloid leukemia (CML), 15 patients with accelerated phase (n=6) or blast crisis (n=9) were enrolled in this study. All the patients were conditioned with cyclophosphamide and busulfan, and treated with cyclosporin (CsA)/methotrexate (MTX)/mycophenolate mofetil (MMF) for graft-versus-host disease (GVHD) prophylaxis. Eleven of these 15 patients (73.3%) achieved complete hematologic response to pre-transplant imatinib, and six (40%) achieved a cytogenetic response. No engraftment failure was observed and the early transplant-related mortality was only 6.7%. Grade 3/4 acute GVHD occurred in 13.3% of patients. Chronic GVHD was observed in 61.5%, including 23.1% suffered from extensive disease. The 5-year estimated rates of relapse, transplant-related mortality and overall survival were 21.0±10.8% 13.7±10.8% and 66.0±12.4%, respectively. Ten (66.7%) of 15 patients are alive with complete molecular remission, even after a median follow-up of 25 months after withdrawal of imatinib. In conclusion, even CML in advanced phases may have a satisfactory outcome after myeloablative allo-HSCT combined with imatinib, which may provide good remission prior to transplantation and reduce relapse risk, with low toxicity.

摘要

为评估清髓性异基因造血干细胞移植(allo-HSCT)联合伊马替尼治疗晚期慢性髓系白血病(CML)的疗效和安全性,本研究纳入 15 例加速期(n=6)或急变期(n=9)患者。所有患者均接受环磷酰胺和白消安预处理,并采用环孢素(CsA)/甲氨蝶呤(MTX)/霉酚酸酯(MMF)预防移植物抗宿主病(GVHD)。15 例患者中 11 例(73.3%)在移植前伊马替尼治疗时达到完全血液学缓解,6 例(40%)达到细胞遗传学缓解。未观察到植入失败,早期移植相关死亡率仅为 6.7%。患者中 13.3%发生 3/4 级急性 GVHD。61.5%的患者发生慢性 GVHD,其中 23.1%为广泛性疾病。5 年估计复发率、移植相关死亡率和总生存率分别为 21.0±10.8%、13.7±10.8%和 66.0±12.4%。15 例患者中 10 例(66.7%)在停用伊马替尼后中位随访 25 个月时仍存活且完全分子缓解。结论:即使是晚期 CML,经清髓性 allo-HSCT 联合伊马替尼治疗后也可能获得满意的疗效,这可能在移植前提供良好的缓解,并降低复发风险,同时毒性较低。

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