IDH1 and IDH2 mutations are frequent genetic alterations in acute myeloid leukemia and confer adverse prognosis in cytogenetically normal acute myeloid leukemia with NPM1 mutation without FLT3 internal tandem duplication.
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Summary
IDH1 and IDH2 mutations are recurring genetic changes in AML that constitute a poor prognostic factor in CN-AML with mutated NPM1 without FLT3-ITD, which allows refined risk stratification of this AML subset.
- Type
- article
- Published
- 2010-08-01
- Cited by
- 811
- References
- 45
- OpenAlex
- https://openalex.org/W2152496375
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:34532973
Keywords
NPM1, IDH2, CEBPA, Myeloid leukemia, Medicine
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Cited by
- IDH1 and IDH2 mutations in myeloid neoplasms – Novel paradigms and clinical implications
- Leukemia stem cells and microenvironment: biology and therapeutic targeting.
- Impact of molecular prognostic factors in cytogenetically normal acute myeloid leukemia at diagnosis and relapse
- NCCN Task Force report: Evaluating the clinical utility of tumor markers in oncology.
- Lessons from next-generation sequencing analysis in hematological malignancies
- Molecular evaluation of DNMT3A and IDH1/2 gene mutation: frequency, distribution pattern and associations with additional molecular markers in normal karyotype Indian acute myeloid leukemia patients.
- New Developments in the Pathogenesis and Therapeutic Targeting of the IDH1 Mutation in Glioma
- Next Generation Sequencing of Acute Myeloid Leukemia: Influencing Prognosis
- Hematopoietic stem cell transplantation for adult patients with isolated NPM1 mutated acute myeloid leukemia in first remission
- Emerging drug profile: Krebs cycle and cancer: IDH mutations and therapeutic implications
- Manipulation du métabolisme énergétique dans les leucémies aiguës myéloïdes : mitochondrie, apoptose et mécanisme d'action de la metformine
- Acute Myeloid Leukemia, Genetics, and Risk Stratification: Data Overload or Ready for a Breakthrough?
- Topics in cancer genomics
- Studies on CEBPA mutations in acute myeloid leukaemia
- Mutations de gènes impliqués dans le métabolisme énergétique et cancer
- Aktuelle Behandlungsmöglichkeiten akuter myeloischer Leukämien
- Prognostic markers in pediatric leukemia and mechanisms of KRAS induced leukemogenesis
- Rôle des anomalies de TET2 dans la transformation tumorale lymphoïde et myéloïde
- Cytosine modifications in myeloid malignancies.
- Molecular Characterization of Genetic and Epigenetic Alterations in Gliomas
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