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. 2025 Aug 22;15(8):e095640. doi: 10.1136/bmjopen-2024-095640

Table 2. Bone marrow features and 2022 WHO classification for confirmed suspicions of myelodysplastic neoplasms (n=37).

MDS features
Bone marrow blasts, median (IQR), % 2.5 (1.8–5.5)
Any bone marrow cytogenetic abnormality, n (%)* 19/36 (53)
Any bone marrow somatic mutation, n (%)† 25/26 (96)
Bone marrow flow cytometric score≥2, n (%)‡ 26/35 (74)
2022 WHO classification, n (%)
 MDS with defining genetic abnormalities
 MDS with low blasts and SF3B1 mutation (MDS-SF3B1) 4 (11)
 MDS with low blasts and ring sideroblasts (wild-type SF3B1) 1 (2.7)
 MDS with biallelic TP53 inactivation (MDS-biTP53) 1 (2.7)
 MDS morphologically defined
 MDS with low blasts (MDS-LB) 17 (46)
 MDS with increased blasts 1 (MDS-IB1) 5 (14)
 MDS with increased blasts 2 (MDS-IB2) 5 (14)
 Chronic myelomonocytic leukaemia (CMML1) 4 (11)
International Prognostic Scoring System, n (%)
 Low/intermediate-1 29 (78)
 Intermediate-2/high 8 (22)
Revised International Prognostic Scoring System, n (%)
 Very low/low/intermediate 27 (73)
 High/very high 10 (27)
*

Bone marrow karyotype was not available for one patient.

†

Molecular profiling was not available for 11 patients.

‡

Bone marrow flow cytometric24 score was computed as the number of parameters with values outside of the reference ranges among myeloblast-related cluster size in all nucleated cells (%), B-progenitor-related cluster size in all CD34+ cells (%), lymphocytes to myeloblast CD45 ratio and granulocyte to lymphocyte SSC ratio. Bone marrow flow cytometric score was not available for two patients.

MDS, myelodysplastic neoplasm.