Bone Marrow Transplant Center, The First Affiliated Hospital, School of Medicine, Zhejiang University, 79 Qingchun Road, Hangzhou, China.
Leuk Res. 2011 Oct;35(10):1307-11. doi: 10.1016/j.leukres.2011.01.001. Epub 2011 Feb 26.
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.
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。