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Allogeneic haematopoietic SCT for chronic myelomonocytic leukaemia:a single-centre experience

机译:异基因造血干细胞移植治疗慢性粒细胞性白血病的单中心经验

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摘要

Haematopoietic SCT (HSCT) offers the only potentially curative option in chronic myelomonocytic leukaemia (CMML). In this study, we report on single-centre results of 18 patients with CMML who have undergone allogeneic HSCT. The median age of patients was 54 years. Seven patients had AML, which had transformed from CMML. Overall, 11 patients received stem cells from an unrelated donor. A total of 15 patients received a T-cell-depleted fludarabine/BU-based reduced-intensity conditioning HSCT. The actuarial 3-year OS, non-relapse mortality (NRM) and relapse incidence for the cohort was 31 +/- 11%, 31 +/- 14% and 47 +/- 13%, respectively. Patients with favourable cytogenetics had a 3-year disease-free survival of 65 +/- 17%, whereas none of the seven patients with intermediate or poor risk cytogenetics survived beyond 2 years (P <0.01). No patients with favourable risk cytogenetics died from NRM causes, while the 2-year NRM for the intermediate/poor risk cytogenetics subgroup was 71 +/- 22% (P <0.02). In terms of disease status at transplantation, patients who had <5% BM blasts had a 3-year disease-free survival of 46.9 +/- 19% compared with those with > 5% blasts at the time of transplantation (that is, 20.0 +/- 13%). Recipient age, type of conditioning regimen or stem cell dose did not have a significant impact on overall outcomes. Our data support existing evidence that allogeneic HSCT is a feasible therapeutic option for CMML, with the ability to attain long-term remission among patient subgroups.
机译:造血干细胞移植(HSCT)在慢性粒细胞单核细胞白血病(CMML)中提供了唯一可能的治疗选择。在这项研究中,我们报告了接受异体HSCT的18例CMML患者的单中心结果。患者的中位年龄为54岁。七名患有AML的患者已从CMML转变为AML。总体而言,有11名患者从无关亲戚那里获得了干细胞。共有15位患者接受了基于T细胞的氟达拉滨/ BU降低强度调理HSCT。该人群的精算3年OS,非复发死亡率(NRM)和复发发生率分别为31 +/- 11%,31 +/- 14%和47 +/- 13%。具有良好细胞遗传学功能的患者的3年无病生存率为65 +/- 17%,而具有中等或较弱风险细胞遗传学功能的7例患者均没有生存超过2年的时间(P <0.01)。没有风险细胞遗传学有利的患者死于NRM原因,而中度/不良风险细胞遗传学亚组的2年NRM为71 +/- 22%(P <0.02)。就移植时的疾病状态而言,与5%BM blast相比,那些BM blast≥5%的患者3年无病生存率为46.9 +/- 19%(20.0) +/- 13%)。接受者的年龄,调理方案的类型或干细胞的剂量对总体结果没有显着影响。我们的数据支持现有证据,即同种异体HSCT是CMML可行的治疗选择,能够在患者亚组中实现长期缓解。

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