Co-occurrence of cohesin complex and Ras signaling mutations during progression from myelodysplastic syndromes to secondary acute myeloid leukemia

Myelodysplastic syndromes (MDS) are hematological disorders at high risk of progression to secondary acute myeloid leukemia (sAML). However, the mutational dynamics and clonal evolution underlying disease progression are poorly understood at present. In order to elucidate the mutational dynamics of pathways and genes occurring during the evolution to sAML, next-generation sequencing was performed on 84 serially paired samples of MDS patients who developed sAML (discovery cohort) and 14 paired samples from MDS patients who did not progress to sAML during follow-up (control cohort). Results were validated in an independent series of 388 MDS patients (validation cohort). We used an integrative analysis to identify how mutations, alone or in combination, contribute to leukemic transformation. The study showed that MDS progression to sAML is characterized by greater genomic instability and the presence of several types of mutational dynamics, highlighting increasing (STAG2) and newly acquired (NRAS and FLT3) mutations. Moreover, we observed co-operation between genes involved in the cohesin and Ras pathways in 15-20% of MDS patients who evolved to sAML, as well as a high proportion of newly acquired or increasing mutations in the chromatin-modifier genes in MDS patients receiving a disease-modifying therapy before their progression to sAML.

Automated summary

The study revealed that MDS progression to sAML is characterized by greater genomic instability and various types of mutational dynamics, particularly highlighting increased (STAG2) and newly acquired (NRAS and FLT3) mutations. Cooperation between genes in the Ras and cohesin pathways were observed in 15-20% of MDS patients who evolved to sAML, along with a high proportion of newly acquired or increasing mutations in chromatin-modifier genes in MDS patients treated with disease-modifying therapy before progressing to sAML.