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成人急性髓系白血病伴不确定细胞遗传学分析患者的基因突变谱、结局和异基因造血干细胞移植的影响。

Mutational profile, outcomes, and impact of allogeneic hematopoietic stem cell transplantation in adult patients with acute myeloid leukemia and inconclusive cytogenetic analysis.

机构信息

The Ottawa Hospital Bone Marrow Transplant Programme, University of Ottawa, Ottawa, Ontario, Canada.

Leukemia Program, Princess Margaret Cancer Centre, University of Toronto, Toronto, Ontario, Canada.

出版信息

Eur J Haematol. 2023 Jun;110(6):618-625. doi: 10.1111/ejh.13940. Epub 2023 Feb 16.

Abstract

BACKGROUND

Inconclusive cytogenetic analysis (IC) at baseline has been reported as a predictor of poor prognosis in patients with acute myeloid leukemia (AML). The mutational profile in this group of patients, and its impact on outcomes have not been reported.

METHODS

We retrospectively analyzed adult patients (≥18 years) with newly diagnosed AML treated with intensive induction chemotherapy between 2015 and 2019. Patients with any documented cytogenetic abnormalities were excluded. Targeted next generation sequencing (NGS) was performed in all patients. Baseline characteristics, mutation profile, and outcomes were compared between patients with normal cytogenetics(NC) and those with IC.

RESULTS

Sixty-one patients (males 39.3%; median age 59 years) had IC at diagnosis. The proportion of patients with mutations in genes with proven prognostic impact were not different between AML patients with IC and NC. AML patients with NC were more likely to harbor the prognostically favorable NPM1 /FLT3-ITD mutational combination conferring "favorable" risk status. As a result, a larger proportion of patients in the IC group underwent allogeneic hematopoietic stem cell transplantation (allo HCT; 54.1% vs. 39.6%; p = .02). The 2-year RFS (55.9% vs. 58.5%; p = .29) and OS (61.9% vs. 66.9%; p = .48) were similar in IC and NC patients. There was no difference in survival of patients who underwent allo HCT when compared with patients who did not (p = .99).

CONCLUSIONS

Inconclusive cytogenetic analysis may not be an independent prognostic indicator in AML. In such patients, molecular abnormalities detected through NGS or whole genome sequencing are more likely to be informative.

摘要

背景

基线时不确定的细胞遗传学分析(IC)已被报道为急性髓系白血病(AML)患者预后不良的预测因子。该组患者的突变谱及其对结果的影响尚未报道。

方法

我们回顾性分析了 2015 年至 2019 年间接受强化诱导化疗的新诊断为 AML 的成年患者(≥18 岁)。排除有任何明确细胞遗传学异常的患者。所有患者均进行靶向下一代测序(NGS)。比较细胞遗传学正常(NC)和 IC 患者的基线特征、突变谱和结局。

结果

61 例患者(男性占 39.3%;中位年龄 59 岁)在诊断时存在 IC。IC 和 NC 的 AML 患者基因突变具有明确预后影响的比例无差异。NC 的 AML 患者更有可能携带预后良好的 NPM1/FLT3-ITD 突变组合,赋予“有利”的风险状态。因此,IC 组中更多的患者接受异基因造血干细胞移植(allo HCT;54.1% vs. 39.6%;p=0.02)。2 年 RFS(55.9% vs. 58.5%;p=0.29)和 OS(61.9% vs. 66.9%;p=0.48)在 IC 和 NC 患者中相似。与未接受 allo HCT 的患者相比,接受 allo HCT 的患者的生存无差异(p=0.99)。

结论

不确定的细胞遗传学分析可能不是 AML 的独立预后指标。在这些患者中,通过 NGS 或全基因组测序检测到的分子异常更有可能具有信息性。

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