Medication Adherence to Tyrosine Kinase Inhibitors: 2-Year Analysis of Medication Adherence to Imatinib Treatment for Chronic Myeloid Leukemia and Correlation with the Depth of Molecular Response

Acta Haematol. 2016;136(1):45-51. doi: 10.1159/000444626. Epub 2016 May 10.

Abstract

Objective: Adherence to tyrosine kinase inhibitor treatment is a significant factor in the achievement of a good clinical response in chronic myeloid leukemia (CML). The aim of this retrospective study is to investigate 1- and 2-year medication adherence to imatinib treatment, linking adherence rates with the clinical outcome, in accordance with European LeukemiaNet Recommendations for the management of CML. We have tried to find a cutoff value for adherence in order to achieve a good clinical outcome.

Methods: The method used to calculate medication adherence was the ratio between the received and the prescribed daily dose.

Results: We observed the levels of mean adherence for each of the following response groups (in years 1 and 2, respectively): complete response (0.96, 0.95), MR4.5 (1.00, -), MR4 (0.93, 0.91), major molecular responses (0.96, 0.97), warning (0.91, 0.89) and failure (0.79, 0.84).

Conclusion: Results show that the higher the adherence, the lower the level of BCR-ABL1. Furthermore, using cutoffs ≥0.9, outcomes were significantly improved compared to those with cutoffs <0.90. This value of adherence is in line with previous publications.

Publication types

  • Comment

MeSH terms

  • Antineoplastic Agents / therapeutic use
  • Benzamides / therapeutic use
  • Fusion Proteins, bcr-abl / therapeutic use
  • Humans
  • Imatinib Mesylate*
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / drug therapy
  • Medication Adherence*
  • Piperazines / therapeutic use
  • Protein Kinase Inhibitors / therapeutic use
  • Protein-Tyrosine Kinases / therapeutic use
  • Pyrimidines / therapeutic use
  • Retrospective Studies
  • Treatment Outcome

Substances

  • Antineoplastic Agents
  • Benzamides
  • Piperazines
  • Protein Kinase Inhibitors
  • Pyrimidines
  • Imatinib Mesylate
  • Protein-Tyrosine Kinases
  • Fusion Proteins, bcr-abl