The prognostic role of NKG2A expression for patients with chronic myeloid leukemia after treatment discontinuation

Leuk Lymphoma. 2022 Nov;63(11):2616-2626. doi: 10.1080/10428194.2022.2090549. Epub 2022 Jun 25.

Abstract

This study aims to evaluate the possibility of tyrosine kinase inhibitors (TKIs) discontinuation in chronic myeloid leukemia (CML) patients who obtained sustained deep molecular response (DMR) and to explore the prognostic role of NK cells in treatment-free remission (TFR). Sixty CML patients who discontinued TKI treatment were enrolled, and we also investigated the immune profiles in 27 CML patients after TKI cessation. Of the 60 patients, the estimated TFR rate was 60.8% [95% CI: 49.5-74.8%] at 12 months. Patients who had longer TKI duration, major molecular response, and DMR maintenance time had a significantly higher TFR rate. And a higher percentage of NKG2A+NK cells and NKG2A+CD56brightCD16-NK cells were independent prognostic factors of TFR in multivariate analysis. These results indicate the practicality of the cessation of TKIs and patients with stable NK cell counts accompanied by higher cytotoxicity and increased killing capacity are more inclined to get sustained treatment-free survival.

Keywords: Chronic myeloid leukemia (CML); NKG2A; NKG2D; natural killer (NK) cells; treatment-free remission (TFR); tyrosine kinase inhibitor (TKI).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Humans
  • Killer Cells, Natural
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive* / diagnosis
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive* / drug therapy
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive* / genetics
  • Prognosis
  • Protein Kinase Inhibitors* / adverse effects
  • Remission Induction
  • Treatment Outcome

Substances

  • Protein Kinase Inhibitors