首页> 外文期刊>Biology of blood and marrow transplantation: journal of the American Society for Blood and Marrow Transplantation >Allogeneic hematopoietic cell transplantation for chronic myelomonocytic leukemia: relapse-free survival is determined by karyotype and comorbidities.
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Allogeneic hematopoietic cell transplantation for chronic myelomonocytic leukemia: relapse-free survival is determined by karyotype and comorbidities.

机译:用于慢性粒单核细胞白血病的同种异体造血细胞移植:无复发生存取决于核型和合并症。

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摘要

Hematopoietic cell transplantation (HCT) offers potentially curative therapy for chronic myelomonocytic leukemia (CMML). We evaluated HCT outcomes in 85 patients with CMML, 1.0-69.1 (median 51.7) years of age, with follow-up extending to 19 years. CMML was considered de novo in 71 and secondary in 14 patients. Conditioning regimens were of various intensities. Thirty-eight patients had related (34 HLA identical), and 47 (39 HLA matched) unrelated donors. The source of stem cells was marrow in 32 and peripheral blood progenitor cells in 53 patients. Acute graft-versus-host disease (aGVHD) grades II-IV occurred in 72% and chronic GVHD (cGVHD) in 26% of patients. Relapse incidence was 27% at 10 years. Relapse correlated with increasing scores by the MD Anderson prognostic score (P = .01). The major causes of death were relapse and infections +/-GVHD. Progression-free survival (PFS) was 38% at 10 years. Mortality was negatively correlated with pre-HCT hematocrit (P = .007), and increased with high-risk cytogenetics (P = .02), higher HCT Comorbidity Index (P = .0008), and increased age (P = .02). WHO classification did not statistically significantly affect outcome. Thus, a proportion of patients with CMML have lasting remissions following allogeneic HCT and appear to be cured of their disease.
机译:造血细胞移植(HCT)为慢性粒细胞单核细胞白血病(CMML)提供了潜在的治疗方法。我们评估了85例1.0-69.1岁(平均51.7岁)的CMML患者的HCT结局,随访时间延长至19年。 CMML在71例中被认为是新生,在14例中是继发性。调理方案的强度各不相同。 38位患者有相关的(34位HLA相同)和47位(39位HLA匹配)无关的供体。干细胞的来源是32位患者的骨髓,而53位患者的外周血祖细胞。急性移植物抗宿主病(aGVHD)的II-IV级发生在72%,慢性GVHD(cGVHD)发生在26%的患者中。 10年时复发率是27%。复发与MD安德森预后评分的增加(P = 0.01)相关。死亡的主要原因是复发和感染+/- GVHD。 10年无进展生存率(PFS)为38%。死亡率与HCT之前的血细胞比容呈负相关(P = .007),并且随着高危细胞遗传学(P = .02),HCT合并症指数(P = .0008)和年龄增加(P = .02)而增加。 。 WHO分类没有统计学上显着影响预后。因此,相当一部分CMML患者在异基因HCT之后具有持久的缓解,并且似乎可以治愈他们的疾病。

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