Figure 2.
Clinical course of lenalidomide-associated ALL in one patient. (A) Clinical course of patient #9, who was found to have an immature B-cell population with B-ALL immunophenotype at 48 months into lenalidomide maintenance for MM, with regression of B-ALL after lenalidomide withdrawal and subsequent progression to overt B-ALL at 284 days from the initial finding of abnormal B lymphoblasts. He received B-ALL therapy consisting of hyper-CVAD followed by blinatumomab and achieved CR with MRD negativity, followed by haploidentical allogeneic HCT and remains in continuous, ongoing MRD− CR. Flow cytometry plots from BMAs and TdT immunostains on core biopsies depict evolution in B-lymphoblast population from initial finding 48 months into lenalidomide maintenance (B,E) to regression after lenalidomide withdrawal (C,F) to overt progression to B-ALL (D,G). All blast percentages are from BMAs.

Clinical course of lenalidomide-associated ALL in one patient. (A) Clinical course of patient #9, who was found to have an immature B-cell population with B-ALL immunophenotype at 48 months into lenalidomide maintenance for MM, with regression of B-ALL after lenalidomide withdrawal and subsequent progression to overt B-ALL at 284 days from the initial finding of abnormal B lymphoblasts. He received B-ALL therapy consisting of hyper-CVAD followed by blinatumomab and achieved CR with MRD negativity, followed by haploidentical allogeneic HCT and remains in continuous, ongoing MRD CR. Flow cytometry plots from BMAs and TdT immunostains on core biopsies depict evolution in B-lymphoblast population from initial finding 48 months into lenalidomide maintenance (B,E) to regression after lenalidomide withdrawal (C,F) to overt progression to B-ALL (D,G). All blast percentages are from BMAs.

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