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. 2025 Nov 25;9(11):e70256.
doi: 10.1002/hem3.70256. eCollection 2025 Nov.

Inflammatory disorders in IDH-mutated myeloid neoplasms: Characteristics and response to IDH inhibitors

Affiliations

Inflammatory disorders in IDH-mutated myeloid neoplasms: Characteristics and response to IDH inhibitors

Romain Stammler et al. Hemasphere. .
No abstract available

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Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
Cytokine profiling in immune‐mediated inflammatory disorder (IMID) patients with IDH mut or IDH wt myeloid neoplasms, and therapeutic efficacy of biotherapies and anti‐IDH inhibitors in IMID‐IDH mut patients. (A) Volcano plots showing upregulated (right) and downregulated (left) cytokines and chemokines between IDHmut and IDHwt. The green dashed line marks the significance threshold. Only significant cytokines are labeled. Global comparison of upregulated and downregulated cytokines between IDHmut and IDHwt groups. (B) Evolution of overall inflammatory response rates over time with biotherapies and azacitidine treatments. (C) Evolution of overall inflammatory response rates, steroid dosage, and C‐reactive protein level over time with IDH inhibitors. (D) Cytokine profile pre‐ and post‐ivosidenib (anti‐IDH1) in one patient showing log2 fold changes in circulating cytokines and chemokines, with upregulated (red) and downregulated (blue) markers. D‐2‐HG and C‐reactive protein (CRP) levels evolution under anti‐IDH1 inhibitor in the same patient. IL, interleukin‐6; TNF, tumor necrosis factor.

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