PMID- 33834631 OWN - NLM STAT- MEDLINE DCOM- 20211129 LR - 20211129 IS - 1751-553X (Electronic) IS - 1751-5521 (Linking) VI - 43 IP - 5 DP - 2021 Oct TI - Leukemic stem cells shall be searched in the bone marrow before "tyrosine kinase inhibitor-discontinuation" in chronic myeloid leukemia. PG - 1110-1116 LID - 10.1111/ijlh.13528 [doi] AB - 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/muL (16-737.5 LSC/muL), and 805 LSC/10(6) WBCs (134.6-2470 LSC/10(6) 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/muL (0-248.7 LSC/muL) and 143.5 LSC/10(6) WBCs (9-455.2 LSC/10(6) 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/10(6) WBCs (3.1-613.7 LSC/10(6) 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. CI - (c) 2021 John Wiley & Sons Ltd. FAU - Ilhan, Osman AU - Ilhan O AD - Department of Hematology, Ankara University School of Medicine, Ankara, Turkey. FAU - Narli Ozdemir, Zehra AU - Narli Ozdemir Z AUID- ORCID: 0000-0003-3237-320X AD - Department of Hematology, Ministry of Health Ankara City Hospital, Ankara, Turkey. FAU - Dalva, Klara AU - Dalva K AD - Department of Hematology, Ankara University School of Medicine, Ankara, Turkey. FAU - Arslan, Aysenur AU - Arslan A AD - Department of Hematology, Ege University School of Medicine, Izmir, Turkey. FAU - Okay Ozgeyik, Mufide AU - Okay Ozgeyik M AD - Department of Hematology, Ministry of Health Eskisehir City Hospital, Eskisehir, Turkey. FAU - Ipek, Senay AU - Ipek S AD - Department of Hematology, Ankara University School of Medicine, Ankara, Turkey. FAU - Saydam, Guray AU - Saydam G AD - Department of Hematology, Ege University School of Medicine, Izmir, Turkey. FAU - Haznedaroglu, Ibrahim C AU - Haznedaroglu IC AD - Department of Hematology, Hacettepe University School of Medicine, Ankara, Turkey. LA - eng GR - 54173265/Pfizer/ PT - Journal Article DEP - 20210409 PL - England TA - Int J Lab Hematol JT - International journal of laboratory hematology JID - 101300213 RN - 0 (Protein Kinase Inhibitors) RN - EC 2.7.10.1 (Protein-Tyrosine Kinases) SB - IM MH - Adult MH - Aged MH - Aged, 80 and over MH - Bone Marrow/*drug effects/pathology MH - Cohort Studies MH - Female MH - Humans MH - Leukemia, Myelogenous, Chronic, BCR-ABL Positive/*drug therapy/pathology MH - Male MH - Middle Aged MH - Neoplastic Stem Cells/*drug effects/pathology MH - Protein Kinase Inhibitors/*therapeutic use MH - Protein-Tyrosine Kinases/antagonists & inhibitors OTO - NOTNLM OT - CML OT - flow cytometry OT - stem cell EDAT- 2021/04/10 06:00 MHDA- 2021/11/30 06:00 CRDT- 2021/04/09 06:50 PHST- 2021/03/03 00:00 [revised] PHST- 2020/12/24 00:00 [received] PHST- 2021/03/09 00:00 [accepted] PHST- 2021/04/10 06:00 [pubmed] PHST- 2021/11/30 06:00 [medline] PHST- 2021/04/09 06:50 [entrez] AID - 10.1111/ijlh.13528 [doi] PST - ppublish SO - Int J Lab Hematol. 2021 Oct;43(5):1110-1116. doi: 10.1111/ijlh.13528. Epub 2021 Apr 9.