Clinical utility of next-generation sequencing in acute myeloid leukemia

F Yang, T Anekpuritanang, RD Press - Molecular diagnosis & therapy, 2020 - Springer
Acute myeloid leukemia (AML) is a genetically heterogeneous disease that, even with
current advancements in therapy, continues to have a poor prognosis. Recurrent somatic …

Genetic aspects of myelodysplastic/myeloproliferative neoplasms

L Palomo, P Acha, F Solé - Cancers, 2021 - mdpi.com
Simple Summary Myelodysplastic/myeloproliferative neoplasms (MDS/MPN) are clonal
myeloid neoplasms characterized, at the time of their presentation, by the simultaneous …

DDX41 germline variants causing donor cell leukemia indicate a need for further genetic workup in the context of hematopoietic stem cell transplantation

B Rolles, R Meyer, M Begemann, M Elbracht… - Blood Cancer …, 2023 - nature.com
Hematopoietic stem cell transplantation (HSCT) represents the standard treatment for
patients with high or intermediate-2 risk (IPSS classification) myelodysplastic syndrome …

Assessing acquired resistance to IDH1 inhibitor therapy by full-exon IDH1 sequencing and structural modeling

ZN Oltvai, SE Harley, D Koes… - Molecular …, 2021 - molecularcasestudies.cshlp.org
Somatic mutations in hotspot regions of the cytosolic or mitochondrial isoforms of the
isocitrate dehydrogenase gene (IDH1 and IDH2, respectively) contribute to the …

Myelodysplasia cutis

CP Whittington, CW Ross… - … of Pathology & …, 2024 - meridian.allenpress.com
Context.—Myelodysplasia cutis is an emerging concept in cutaneous neoplasia. Many of
these cases were previously included under the umbrella of histiocytoid Sweet syndrome …

Haematologic malignancies with unfavourable gene mutations benefit from donor lymphocyte infusion with/without decitabine for prophylaxis of relapse after …

R Zhang, L Wang, P Chen, X Gao, S Wang… - Cancer …, 2021 - Wiley Online Library
Relapse is the main cause of treatment failure for leukaemia patients with unfavourable
gene mutations who receive allogeneic haematopoietic stem cell transplantation (allo …

Technical validation and clinical utility of an NGS targeted panel to improve molecular characterization of pediatric acute leukemia

C Vicente-Garcés, E Esperanza-Cebollada… - Frontiers in Molecular …, 2022 - frontiersin.org
Development of next-generation sequencing (NGS) has provided useful genetic information
to redefine diagnostic, prognostic, and therapeutic strategies for the management of acute …

Gene mutation analysis using next‐generation sequencing and its clinical significance in patients with myeloid neoplasm: A multi‐center study from China

J Li, L Pei, S Liang, S Xu, Y Wang, X Wang… - Cancer …, 2023 - Wiley Online Library
Background Myeloid neoplasms (MN) tend to relapse and deteriorate. Exploring the
genomic mutation landscape of MN using next‐generation sequencing (NGS) is a great …

[HTML][HTML] Clinical utility of targeted next-generation sequencing assay to detect copy number variants associated with myelodysplastic syndrome in myeloid …

L Jiang, A Pallavajjala, J Huang, L Haley… - The Journal of Molecular …, 2021 - Elsevier
Copy number variants (CNVs) and gene mutations are important for diagnosis and treatment
of myeloid malignancies. In a routine clinical setting, somatic gene mutations are detected …

Clusterization in acute myeloid leukemia based on prognostic alternative splicing signature to reveal the clinical characteristics in the bone marrow microenvironment

N Zhang, P Zhang, Y Chen, S Lou, H Zeng, J Deng - Cell & bioscience, 2020 - Springer
Background Alternative splicing (AS), a crucial post-transcriptional regulatory mechanism in
expanding the coding capacities of genomes and increasing the diversity of proteins, still …