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验证和完善 2017 年修订的欧洲白血病网络急性髓系白血病遗传风险分层。

Validation and refinement of the revised 2017 European LeukemiaNet genetic risk stratification of acute myeloid leukemia.

机构信息

Laboratory for Leukemia Diagnostics, Department of Medicine III, University Hospital, LMU Munich, Munich, Germany.

German Cancer Consortium (DKTK), Partner Site Munich, Munich, Germany.

出版信息

Leukemia. 2020 Dec;34(12):3161-3172. doi: 10.1038/s41375-020-0806-0. Epub 2020 Mar 30.

DOI:10.1038/s41375-020-0806-0
PMID:32231256
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7685975/
Abstract

The revised 2017 European LeukemiaNet (ELN) recommendations for genetic risk stratification of acute myeloid leukemia have been widely adopted, but have not yet been validated in large cohorts of AML patients. We studied 1116 newly diagnosed AML patients (age range, 18-86 years) who had received induction chemotherapy. Among 771 patients not selected by genetics, the ELN-2017 classification re-assigned 26.5% of patients into a more favorable or, more commonly, a more adverse-risk group compared with the ELN-2010 recommendations. Forty percent of the cohort, and 51% of patients ≥60 years, were classified as adverse-risk by ELN-2017. In 599 patients <60 years, estimated 5-year overall survival (OS) was 64% for ELN-2017 favorable, 42% for intermediate-risk and 20% for adverse-risk patients. Among 517 patients aged ≥60 years, corresponding 5-year OS rates were 37, 16, and 6%. Patients with biallelic CEBPA mutations or inv(16) had particularly favorable outcomes, while patients with mutated TP53 and a complex karyotype had especially poor prognosis. DNMT3A mutations associated with inferior OS within each ELN-2017 risk group. Our results validate the prognostic significance of the revised ELN-2017 risk classification in AML patients receiving induction chemotherapy across a broad age range. Further refinement of the ELN-2017 risk classification is possible.

摘要

修订后的 2017 年欧洲白血病网络(ELN)急性髓系白血病遗传风险分层建议已被广泛采用,但尚未在大量 AML 患者队列中得到验证。我们研究了 1116 例新诊断的 AML 患者(年龄 18-86 岁),他们接受了诱导化疗。在未通过遗传学选择的 771 例患者中,与 ELN-2010 建议相比,ELN-2017 分类将 26.5%的患者重新分配到更有利或更不利的风险组。该队列的 40%,和 51%的年龄≥60 岁的患者,按照 ELN-2017 被分类为不良风险。在 599 例年龄<60 岁的患者中,ELN-2017 有利、中间风险和不良风险患者的估计 5 年总生存率(OS)分别为 64%、42%和 20%。在 517 例年龄≥60 岁的患者中,相应的 5 年 OS 率分别为 37%、16%和 6%。具有双等位基因 CEBPA 突变或 inv(16)的患者具有特别有利的结局,而具有突变 TP53 和复杂核型的患者具有特别差的预后。DNMT3A 突变与 ELN-2017 每个风险组内的 OS 降低相关。我们的结果验证了修订后的 ELN-2017 风险分类在接受诱导化疗的 AML 患者中的预后意义,涵盖了广泛的年龄范围。ELN-2017 风险分类的进一步细化是可能的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/032c/7685975/e9a92f38df24/41375_2020_806_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/032c/7685975/a348064110f0/41375_2020_806_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/032c/7685975/986091f0e9a1/41375_2020_806_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/032c/7685975/56439f2d6f79/41375_2020_806_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/032c/7685975/b33ed737b382/41375_2020_806_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/032c/7685975/e9a92f38df24/41375_2020_806_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/032c/7685975/a348064110f0/41375_2020_806_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/032c/7685975/6c8add9f554c/41375_2020_806_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/032c/7685975/986091f0e9a1/41375_2020_806_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/032c/7685975/56439f2d6f79/41375_2020_806_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/032c/7685975/b33ed737b382/41375_2020_806_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/032c/7685975/e9a92f38df24/41375_2020_806_Fig6_HTML.jpg

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