Leukemic stem cell persistence in chronic myeloid leukemia patients with sustained undetectable molecular residual disease

Author:

Chomel Jean-Claude12,Bonnet Marie-Laure2,Sorel Nathalie12,Bertrand Angelina2,Meunier Marie-Claude2,Fichelson Serge3,Melkus Michael4,Bennaceur-Griscelli Annelise4,Guilhot François25,Turhan Ali G.12

Affiliation:

1. Service d'Hématologie et Oncologie Biologique, CHU de Poitiers, Poitiers, France;

2. Inserm U935, Université de Poitiers, Poitiers, France;

3. Institut Cochin, Inserm U1016, Université Paris Descartes, Paris, France;

4. Inserm U935, Université Paris-Sud 11, Paris, France; and

5. Inserm CIC 0802, CHU de Poitiers, Poitiers, France

Abstract

Abstract Sustained undetectable molecular residual disease (UMRD) is obtained in a minority of patients with chronic myeloid leukemia treated with tyrosine kinase inhibitors. It remains unclear whether these patients are definitively cured of their leukemia or whether leukemic stem cells (LSCs) persist in their BM. We have evaluated the presence of BCR-ABL–expressing marrow LSCs in 6 patients with chronic myeloid leukemia with sustained UMRD induced by IFN-α (n = 3), imatinib mesylate after IFN-α failure (n = 2), and dasatinib after imatinib intolerance (n = 1). Purified CD34+ cells were used for clonogenic and long-term culture-initiating cell assays performed on classic or HOXB4-expressing MS-5 feeders. Using this strategy, we identified BCR-ABL–expressing LSCs in all patients. Interestingly, long-term culture-initiating cell assays with MS-5/HOXB4 stromal feeders increased detected numbers of LSCs in 3 patients. The relation between LSC persistency and a potential risk of disease relapse for patients with durable UMRD (on or off tyrosine kinase inhibitor therapy) warrants further investigation.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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