A clinical observation of Chinese chronic myelogenous leukemia patients after discontinuation of tyrosine kinase inhibitors

Oncotarget. 2016 Sep 6;7(36):58234-58243. doi: 10.18632/oncotarget.11281.

Abstract

Whether tyrosine kinase inhibitors (TKIs) can be safely discontinued is a key focus of chronic myelogenous leukemia (CML) at present. We report a clinical observation of TKIs cessation in Chinese CML patients and a probable connection between CML leukemia stem cells (LSCs) and relapse. In all, 22 of 1057 patients consented to participate in this observation. The average time of complete molecular response was 12.73 months after TKI withdrawal. LSCs could be flow cytometrically detected in most of the patients. However, the number of LSCs did not differ between the relapsers and non-relapsers. We evaluated the leukemogenetic ability of the LSCs by transplanting bone marrow into irradiated NOD/SCID mice. The results indicated that part of the bone marrow from the relapsers lead to leukemogensis in the mice. Besides, we found that LSCs-derived microvesicles might serve as a novel factor for the stratification of undetectable minimal residual disease and an early warning sign of relapse. In summary, post-TKI cessation relapse seems to show none association with the number of LSCs. A mouse xenograft model would provide a novel and useful method of analyzing LSCs function and predicting relapse. Microvesicles may provide important information about optimal molecular monitoring schedules in TKI discontinuation strategies.

Keywords: chronic myelogenous leukemia (CML); discontinuation; leukemia stem cell (LSC); microvesicle (MV); monitoring.

Publication types

  • Observational Study

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Animals
  • Antineoplastic Agents / therapeutic use*
  • Asian People
  • Bone Marrow Transplantation
  • China
  • Drug Resistance, Neoplasm
  • Female
  • Flow Cytometry
  • Humans
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / drug therapy*
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / ethnology*
  • Male
  • Mice
  • Mice, Inbred NOD
  • Mice, SCID
  • Middle Aged
  • Neoplasm Recurrence, Local
  • Neoplasm Transplantation
  • Neoplasm, Residual
  • Neoplastic Stem Cells / drug effects
  • Protein-Tyrosine Kinases / antagonists & inhibitors*
  • Signal Transduction
  • Treatment Outcome
  • Young Adult

Substances

  • Antineoplastic Agents
  • Protein-Tyrosine Kinases