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伴正常核型的治疗相关性急性髓系白血病患者的特征和结局。

Characteristics and outcomes of patients with therapy-related acute myeloid leukemia with normal karyotype.

机构信息

Department of Leukemia, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX, 77030, USA.

Georgia Cancer Center at Augusta University, 1411 Laney Walker Blvd, Augusta, GA, 30912, USA.

出版信息

Blood Cancer J. 2020 May 4;10(5):47. doi: 10.1038/s41408-020-0316-3.

Abstract

Normal karyotype in therapy-related acute myeloid leukemia (t-AML) is rare and the relative contribution of prior exposure to chemotherapy or radiotherapy to outcomes in these patients remains uncertain. We performed a retrospective study of 742 patients with newly diagnosed AML and normal karyotype (t-AML, n = 61, and non-t-AML, n = 681). Patients with t-AML were older but had a similar mutational profile compared to those with non-t-AML. Overall survival (OS) and relapse-free survival (RFS) were significantly worse for patients with t-AML (P < 0.01 and P = 0.02, respectively). Patients with t-AML had a higher cumulative incidence of death in remission (51% versus 16%, P < 0.01), but not higher cumulative incidence of relapse (42% versus 56%, respectively, P = 0.21). Both intensive induction and allogeneic hematopoietic stem cell transplantation in first remission were associated with improved OS and RFS in non-t-AML but not in t-AML. Overall, although disease biology appears similar between t-AML and non-t-AML with normal karyotype as indicated by similar risks of relapse, death in remission is the main driver of inferior outcome in t-AML. Careful therapeutic decisions are required to mitigate potential treatment-related toxicity in this rare subgroup of patients with t-AML and normal karyotype.

摘要

在治疗相关的急性髓系白血病(t-AML)中,正常核型较为罕见,且先前接触化疗或放疗对这些患者结局的相对贡献仍不确定。我们对 742 例新诊断为 AML 且核型正常的患者(t-AML,n=61 例;非 t-AML,n=681 例)进行了回顾性研究。t-AML 患者年龄较大,但与非 t-AML 患者相比,其突变谱相似。t-AML 患者的总生存(OS)和无复发生存(RFS)显著更差(P<0.01 和 P=0.02)。缓解期 t-AML 患者的累积死亡率更高(51%比 16%,P<0.01),但缓解期的累积复发率(42%比 56%,P=0.21)并无差异。强化诱导和异基因造血干细胞移植在非 t-AML 患者中均与 OS 和 RFS 的改善相关,但在 t-AML 患者中则无相关性。总体而言,尽管 t-AML 和核型正常的非 t-AML 患者的疾病生物学似乎相似,复发风险相似,但缓解期的死亡是 t-AML 患者预后不良的主要驱动因素。对于 t-AML 和核型正常这一罕见亚组患者,需要慎重做出治疗决策,以减轻潜在的治疗相关毒性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7d2/7198507/91515575f032/41408_2020_316_Fig1_HTML.jpg

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