DDX41 germline variants causing donor cell leukemia indicate a need for further genetic workup in the context of hematopoietic stem cell transplantation
Author:
Funder
Deutsche Krebshilfe
Publisher
Springer Science and Business Media LLC
Subject
Oncology,Hematology
Link
https://www.nature.com/articles/s41408-023-00846-2.pdf
Reference12 articles.
1. Newell LF, Cook RJ. Advances in acute myeloid leukemia. Br Med J. 2021;375:n2026.
2. Badar T, Nanaa A, He R, Al-Kali A, Viswanatha DS, Godsey E, et al. DDX41 variant of unknown significance (VUS) have distinct clinical and diagnostic features but are associated with similar prognosis and co-mutation patterns as pathogenic DDX41 analysis of the mayo clinic (MC) myeloid next-generation sequencing (NGS) cohort. Blood. 2021;138:3693.
3. Bannon SA, Routbort MJ, Montalban-Bravo G, Mehta RS, Jelloul FZ, Takahashi K, et al. Next-generation sequencing of DDX41 in myeloid neoplasms leads to increased detection of germline alterations. Front Oncol. 2020;10:582213.
4. Duployez N, Largeaud L, Duchmann M, Kim R, Rieunier J, Lambert J, et al. Prognostic impact of DDX41 germline mutations in intensively treated acute myeloid leukemia patients: an ALFA-FILO study. Blood. 2022;140:756–68.
5. Makishima H, Saiki R, Nannya Y, Korotev S, Gurnari C, Takeda J, et al. Germ line DDX41 mutations define a unique subtype of myeloid neoplasms. Blood. 2023;141:534–49.
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Germline Variants and Characteristic Features of Hereditary Hematological Malignancy Syndrome;International Journal of Molecular Sciences;2024-01-04
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