1. Khoury JD, Solary E, Abla O, et al. 2022; The 5th edition of the World Health Organization Classification of Haematolymphoid Tumours: Myeloid and Histiocytic/Dendritic Neoplasms. Leukemia. 36:1703–19. DOI:
10.1038/s41375-022-01613-1. PMID:
35732831. PMCID:
PMC9252913.
Article
2. Alaggio R, Amador C, Anagnostopoulos I, et al. 2022; The 5th edition of the World Health Organization Classification of Haematolymphoid Tumours: Lymphoid Neoplasms. Leukemia. 36:1720–48. DOI:
10.1038/s41375-022-01620-2. PMID:
35732829. PMCID:
PMC9214472.
5. Malcovati L, Stevenson K, Papaemmanuil E, et al. 2020; SF3B1-mutant MDS as a distinct disease subtype: a proposal from the International Working Group for the Prognosis of MDS. Blood. 136:157–70. DOI:
10.1182/blood.2020004850. PMID:
32347921. PMCID:
PMC7362582.
6. Bernard E, Nannya Y, Hasserjian RP, et al. 2020; Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes. Nat Med. 26:1549–56. DOI:
10.1038/s41591-020-1008-z. PMID:
32747829. PMCID:
PMC8381722.
7. Bernard E, Tuechler H, Greenberg PL, et al. 2022; Molecular international prognostic scoring system for myelodysplastic syndromes. NEJM Evid. 1:2022. DOI:
10.1056/EVIDoa2200008. PMID:
38319256.
9. Taube F, Georgi JA, Kramer M, et al. 2022; CEBPA mutations in 4708 patients with acute myeloid leukemia: differential impact of bZIP and TAD mutations on outcome. Blood. 139:87–103. DOI:
10.1182/blood.2020009680. PMID:
34320176.
Article
11. Bataller A, Loghavi S, Gerstein Y, et al. 2023; Characteristics and clinical outcomes of patients with myeloid malignancies and DDX41 variants. Am J Hematol. 98:1780–90. DOI:
10.1002/ajh.27070. PMID:
37665752.
12. Duployez N, Largeaud L, Duchmann M, et al. 2022; Prognostic impact of DDX41 germline mutations in intensively treated acute myeloid leukemia patients: an ALFA-FILO study. Blood. 140:756–68. DOI:
10.1182/blood.2021015328. PMID:
35443031. PMCID:
PMC9389637.
13. Döhner H, Wei AH, Appelbaum FR, et al. 2022; Diagnosis and management of AML in adults: 2022 recommendations from an international expert panel on behalf of the ELN. Blood. 140:1345–77. DOI:
10.1182/blood.2022016867. PMID:
35797463.
Article
15. Ahn JS, Kim HJ. 2022; FLT3 mutations in acute myeloid leukemia: a review focusing on clinically applicable drugs. Blood Res. 57(S1):32–6. DOI:
10.5045/br.2022.2022017. PMID:
35483923. PMCID:
PMC9057665.
16. Walker BA, Boyle EM, Wardell CP, et al. 2015; Mutational spectrum, copy number changes, and outcome: results of a sequencing study of patients with newly diagnosed myeloma. J Clin Oncol. 33:3911–20. DOI:
10.1200/JCO.2014.59.1503. PMID:
26282654. PMCID:
PMC6485456.
Article
17. Manier S, Salem KZ, Park J, Landau DA, Getz G, Ghobrial IM. 2017; Genomic complexity of multiple myeloma and its clinical implications. Nat Rev Clin Oncol. 14:100–13. DOI:
10.1038/nrclinonc.2016.122. PMID:
27531699.
Article
18. Heuser M, Freeman SD, Ossenkoppele GJ, et al. 2021; 2021 Update on MRD in acute myeloid leukemia: a consensus document from the European LeukemiaNet MRD Working Party. Blood. 138:2753–67. DOI:
10.1182/blood.2021013626. PMID:
34724563. PMCID:
PMC8718623.
Article
20. Xie W, Raess PW, Dunlap J, et al. 2022; Adult acute myeloid leukemia patients with NUP98 rearrangement have frequent cryptic translocations and unfavorable outcome. Leuk Lymphoma. 63:1907–16. DOI:
10.1080/10428194.2022.2047672. PMID:
35258401.
21. Bertrums EJM, Smith JL, Harmon L, et al. 2023; Comprehensive molecular and clinical characterization of NUP98 fusions in pediatric acute myeloid leukemia. Haematologica. 108:2044–58. DOI:
10.3324/haematol.2022.281653. PMID:
36815378. PMCID:
PMC10388277.
26. Duncavage EJ, Schroeder MC, O'Laughlin M, et al. 2021; Genome sequencing as an alternative to cytogenetic analysis in myeloid cancers. N Engl J Med. 384:924–35. DOI:
10.1056/NEJMoa2024534. PMID:
33704937. PMCID:
PMC8130455.
Article
27. Ryan SL, Peden JF, Kingsbury Z, et al. 2023; Whole genome sequencing provides comprehensive genetic testing in childhood B-cell acute lymphoblastic leukaemia. Leukemia. 37:518–28. DOI:
10.1038/s41375-022-01806-8. PMID:
36658389. PMCID:
PMC9991920.
Article
32. Svaton M, Skotnicova A, Reznickova L, et al. 2023; NGS better discriminates true MRD positivity for the risk stratification of childhood ALL treated on an MRD-based protocol. Blood. 141:529–33. DOI:
10.1182/blood.2022017003. PMID:
36240445. PMCID:
PMC10651772.
33. Jongen-Lavrencic M, Grob T, Hanekamp D, et al. 2018; Molecular minimal residual disease in acute myeloid leukemia. N Engl J Med. 378:1189–99. DOI:
10.1056/NEJMoa1716863. PMID:
29601269.
Article
34. Patkar N, Kakirde C, Shaikh AF, et al. 2021; Clinical impact of panel-based errorcorrected next generation sequencing versus flow cytometry to detect measurable residual disease (MRD) in acute myeloid leukemia (AML). Leukemia. 35:1392–404. DOI:
10.1038/s41375-021-01131-6. PMID:
33558666. PMCID:
PMC8102181.
Article
36. Kim J, Yun W, Park YJ, et al. 2021; Chimerism assay using single nucleotide polymorphisms adjacent and in linkage-disequilibrium enables sensitive disease relapse monitoring after hematopoietic stem-cell transplantation. Clin Chem. 67:781–7. DOI:
10.1093/clinchem/hvab010. PMID:
33582770.
Article