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The presence of treatment-resistant cancer stem cells has been proposed as a mechanism for disease progression or relapse in many cancer types. Investigators have now explored that possibility in seven patients with myelodysplastic syndrome characterized by chromosome 5q deletion, also called del(5q) myelodysplasia, who had achieved clinical response (i.e., transfusion independence) on lenalidomide therapy.
At baseline and while on treatment, the patients' bone-marrow aspirates were assessed for the presence of clonal stem cells (CD34+, CD90+, and CD38–/low) and clonal progenitor cells (CD34+, CD38+). Key findings included the following:
During lenalidomide treatment, progenitor cells were efficiently targeted and depleted, whereas stem cells…