Volume 43, Issue 5 pp. 1110-1116
ORIGINAL ARTICLE

Leukemic stem cells shall be searched in the bone marrow before “tyrosine kinase inhibitor-discontinuation” in chronic myeloid leukemia

Osman Ilhan

Osman Ilhan

Department of Hematology, Ankara University School of Medicine, Ankara, Turkey

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Zehra Narli Ozdemir

Corresponding Author

Zehra Narli Ozdemir

Department of Hematology, Ministry of Health Ankara City Hospital, Ankara, Turkey

Correspondence

Zehra Narli Ozdemir, Department of Hematology, Ministry of Health Ankara City Hospital, Ankara, Turkey.

Email: [email protected]

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Klara Dalva

Klara Dalva

Department of Hematology, Ankara University School of Medicine, Ankara, Turkey

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Aysenur Arslan

Aysenur Arslan

Department of Hematology, Ege University School of Medicine, İzmir, Turkey

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Mufide Okay Ozgeyik

Mufide Okay Ozgeyik

Department of Hematology, Ministry of Health Eskisehir City Hospital, Eskisehir, Turkey

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Senay Ipek

Senay Ipek

Department of Hematology, Ankara University School of Medicine, Ankara, Turkey

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Guray Saydam

Guray Saydam

Department of Hematology, Ege University School of Medicine, İzmir, Turkey

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Ibrahim C. Haznedaroglu

Ibrahim C. Haznedaroglu

Department of Hematology, Hacettepe University School of Medicine, Ankara, Turkey

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First published: 09 April 2021
Citations: 7

Funding information

Pfizer provided funding support for project # 54173265 through Pfizer Independent Medical Grants program as an independent grant.

Abstract

Background

Leukemic stem cells (LSCs) of chronic myeloid leukemia (CML), persisting in the bone marrow (BM) niche, could be responsible for the relapses within the patients of whom the treatment-free remission (TFR) had been attempted. We assessed the presence of the CML LSCs in the peripheral blood (PB) and concurrently in the BM in the patients with chronic-phase CML (CP CML).

Patients and Methods

Thirty-eight patients with CP CML were included into the study. CD45+/CD34+/CD38 cells with positive CD26 expression were considered as CML LSCs (CD26+ LSC) by using multiparameter flow cytometry (FCM).

Results

Mean BCR-ABL, PB LSC, and BM LSC were 58.528 IS (37.405-83.414 IS), 237.5 LSC/μL (16-737.5 LSC/μL), and 805 LSC/106 WBCs (134.6-2470 LSC/106 WBCs), respectively, in newly diagnosed CML patients. In the patients with BCR-ABL positive hematopoiesis, mean BCR-ABL, PB LSCs, and BM LSCs were 30.09 IS (0.024-147.690 IS), 13.5 LSC/μL (0-248.7 LSC/μL) and 143.5 LSC/106 WBCs (9-455.2 LSC/106 WBCs), respectively. No CML LSCs were detected in PB of patients who achieved deep molecular response (DMR). BM LSCs of the patients who were in DMR were 281.1 LSC/106 WBCs (3.1-613.7 LSC/106 WBCs). The amount of PB LSCs was highest in patients with newly diagnosed CML (P < .001).

Conclusion

LSCs persisted in the BM of the patients with DMR, whereas there was no LSCs in the peripheral blood. The investigation of the CML LSCs in bone marrow before deciding TKI discontinuation could be justified to achieve and maintain stable TFR.

CONFLICT OF INTEREST

The authors have no competing interests.

DATA AVAILABILITY STATEMENT

All relevant data in the paper and its Supporting Information files are deposited to the Ankara University Medical School, Department of Hematology, Ankara-Turkey and are available upon request.

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