期刊
JOURNAL OF HEMATOLOGY & ONCOLOGY
卷 14, 期 1, 页码 -出版社
BMC
DOI: 10.1186/s13045-021-01068-4
关键词
IDH1; IDH2; T-ALL
资金
- Programme Hospitalier de Recherche Clinique, Ministere de l'Emploi et de la Solidarite, France [P0200701, P030425/AOM03081]
- Swiss Federal Government in Switzerland
- Soutien pour la formation a la recherche translationnelle en cancerologie dans le cadre du Plan cancer 2009-2013
- Association pour la Recherche contre le Cancer (Equipe labellisee)
- Institut National du Cancer [PRT-K 18-071]
- Federation Leucemie espoir and Horizon Hemato
- Association Laurette Fugain
- Action Leucemie
IDH2 mutations in T-ALL are associated with older age, an immature phenotype, more frequent RAS gain-of-function mutations, and epigenetic regulator loss-of-function alterations. Conversely, IDH1 mutations appeared to be an independent prognostic factor in multivariate analysis.
IDH1 and IDH2 mutations (IDH1/2(Mut)) are recognized as recurrent genetic alterations in acute myeloid leukemia (AML) and associated with both clinical impact and therapeutic opportunity due to the recent development of specific IDH1/2(Mut) inhibitors. In T-cell acute lymphoblastic leukemia (T-ALL), their incidence and prognostic implications remain poorly reported. Our targeted next-generation sequencing approach allowed comprehensive assessment of genotype across the entire IDH1 and IDH2 locus in 1085 consecutive unselected and newly diagnosed patients with T-ALL and identified 4% of, virtually exclusive (47 of 49 patients), IDH1/2(Mut). Mutational patterns of IDH1/2(Mut) in T-ALL present some specific features compared to AML. Whereas IDH2(R140Q) mutation was frequent in T-ALL (25 of 51 mutations), the IDH2(R172) AML hotspot was absent. IDH2 mutations were associated with older age, an immature phenotype, more frequent RAS gain-of-function mutations and epigenetic regulator loss-of-function alterations (DNMT3A and TET2). IDH2 mutations, contrary to IDH1 mutations, appeared to be an independent prognostic factor in multivariate analysis with the NOTCH1/FBXW7/RAS/PTEN classifier. IDH2(Mut) were significantly associated with a high cumulative incidence of relapse and very dismal outcome, suggesting that IDH2-mutated T-ALL cases should be identified at diagnosis in order to benefit from therapeutic intensification and/or specific IDH2 inhibitors.
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