Novel precision medicine approaches and treatment strategies in hematological malignancies

R Rosenquist, E Bernard, T Erkers… - Journal of Internal …, 2023 - Wiley Online Library
Genetic testing has been applied for decades in clinical routine diagnostics of hematological
malignancies to improve disease (sub) classification, prognostication, patient management …

Emerging molecular subtypes and therapeutic targets in B-cell precursor acute lymphoblastic leukemia

J Li, Y Dai, L Wu, M Zhang, W Ouyang, J Huang… - Frontiers of …, 2021 - Springer
B-cell precursor acute lymphoblastic leukemia (BCP-ALL) is characterized by genetic
alterations with high heterogeneity. Precise subtypes with distinct genomic and/or gene …

Transcriptome-based molecular subtypes and differentiation hierarchies improve the classification framework of acute myeloid leukemia

WY Cheng, JF Li, YM Zhu, XJ Lin… - Proceedings of the …, 2022 - National Acad Sciences
The current classification of acute myeloid leukemia (AML) relies largely on genomic
alterations. Robust identification of clinically and biologically relevant molecular subtypes …

Fusion gene map of acute leukemia revealed by transcriptome sequencing of a consecutive cohort of 1000 cases in a single center

X Chen, F Wang, Y Zhang, X Ma, P Cao, L Yuan… - Blood cancer …, 2021 - nature.com
Fusion genes (FGs) are important genetic abnormalities in acute leukemias, but their variety
and occurrence in acute leukemias remain to be systematically described. Whole …

Long noncoding RNA expression independently predicts outcome in pediatric acute myeloid leukemia

JE Farrar, JL Smith, M Othus, BJ Huang… - Journal of Clinical …, 2023 - ascopubs.org
PURPOSE Optimized strategies for risk classification are essential to tailor therapy for
patients with biologically distinctive disease. Risk classification in pediatric acute myeloid …

Whole transcriptome sequencing detects a large number of novel fusion transcripts in patients with AML and MDS

A Stengel, R Shahswar, T Haferlach, W Walter… - Blood …, 2020 - ashpublications.org
Fusion transcripts are frequent genetic abnormalities in myeloid malignancies and are often
the basis for risk stratification, minimal residual disease (MRD) monitoring, and targeted …

Clinical application of whole transcriptome sequencing for the classification of patients with acute lymphoblastic leukemia

W Walter, R Shahswar, A Stengel, M Meggendorfer… - BMC cancer, 2021 - Springer
Background Considering the clinical and genetic characteristics, acute lymphoblastic
leukemia (ALL) is a rather heterogeneous hematological neoplasm for which current …

Application of precision medicine in clinical routine in haematology—challenges and opportunities

T Wästerlid, L Cavelier, C Haferlach… - Journal of Internal …, 2022 - Wiley Online Library
Precision medicine is revolutionising patient care in cancer. As more knowledge is gained
about the impact of specific genetic lesions on diagnosis, prognosis and treatment response …

[HTML][HTML] Fusion gene detection by RNA-sequencing complements diagnostics of acute myeloid leukemia and identifies recurring NRIP1-MIR99AHG rearrangements

P Kerbs, S Vosberg, S Krebs, A Graf, H Blum… - …, 2022 - ncbi.nlm.nih.gov
Identification of fusion genes in clinical routine is mostly based on cytogenetics and targeted
molecular genetics, such as metaphase karyotyping, fluorescence in situ hybridization and …

Targeted inhibition of the NUP98-NSD1 fusion oncogene in acute myeloid leukemia

S Mohanty, N Jyotsana, A Sharma, A Kloos… - Cancers, 2020 - mdpi.com
Simple Summary NUP98-NSD1-positive acute myeloid leukemia (AML) frequently shows an
additional mutation in Neuroblastoma rat sarcoma (NRAS). However, the synergistic effect of …