Skip to main content
. 2023 Dec 10;143(12):1139–1156. doi: 10.1182/blood.2023021199

Figure 2.

Figure 2.

WHO22 and ICC22 classification criteria analysis for WHOest, WHOnew, and ICCnew cases. (A) Overlap between the reclassified WHOnew and ICCnew cohorts, with the ICCnew cohort being a subgroup of the WHOnew cohort. (B) Overlap between established CMML cases after ICC22 (ICCest) and after WHO22 (WHOest) diagnosis update. (C-F) Classification criteria analysis in the WHOest (subdivided into MD-CMML and MP-CMML), WHOnew, and ICCnew cohorts. (C) Number of cytopenic lineages in the PB. (D) Evidence of clonality. Patients were separated into “no clonality” (maximal VAF <2% of myeloid malignancy associated mutations), VAF between 2% and 10%, and VAF >10% or karyotypical alteration. Only data of patients with ≥10 genes sequenced are shown. (E) Number of dysplastic lineages in the BM. (F) Age-adjusted BM cellularity.