Pharmacogenomics Validation for Imatinib in Chronic Myeloid Leukemia (VATIC)

Asan Medical Center

Status: Completed

Conditions: Leukemia, Myelogenous, Chronic, BCR-ABL Positive

Study type: Observational

Funder types: Other

Identifiers

NCT01437202

AMC-H-64

Details and patient eligibility

About

This is a multicenter, retrospective, observational study to validate a pharmacogenetics model for imatinib metabolism and resistance in patients with chronic myeloid leukemia among patients in different independent cohort.

Full description

1. The activity of Imatinib(IM) is mediated by blocking the activity of BCR/ABL tyrosine kinase in CML cells. However, some of the patients failed to achieve optimal response, and a substantial proportion of patients develop resistance to IM.
2. IM is a substrate for the adenosine triphosphate binding cassette (ABC) transporters, ABCB1 and ABCG2, while the active uptake of IM into cells is mediated by the human organic cationic transporter-1 (hOCT1). Also, IM is metabolized through first pass drug metabolism by the cytochrome P450 - CYP3A4 and CYP3A5. In addition, it is delivered in a bound form with a plasma protein referred to α1-acid glycoprotein (AGP).
3. Accordingly, the intracellular or systemic level of imatinib should be influenced by these factors such as ABCB1, ABCG2, hOCT1, CYP3A4, CYP3A5 or AGP genes. Inter-individual variability of 5 candidate genes associated with drug transport/metabolism (i.e. ABCB1, ABCG2, hOCT1, CYP3A4/3A5 and AGP) could affect the expression of corresponding proteins, thus influencing the treatment outcomes of imatinib therapy.
4. In the investigators' previous study, the investigators reported the cumulative incidences of MCyR and CCyR was significantly affected by the predictive model using 2 genotypes and disease stage. These predictive models for CCyR/MMoR or LOR/treatment failure seemed to work well. However, external validation of these predictive models is warranted especially using ethnically different independent cohort.

Enrollment: 100 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Chronic myeloid leukemia of any stage including chronic phase, accelerated or blastic phase.
• Age>18 years
• Complete set of clinical data available for review (demographic data, stage, treatment history, cytogenetic reports, and latest BCR/ABL RQ-PCR results)
• Treated with imatinib mesylate at least 3 months

Exclusion criteria

• Treated with imatinib mesylate less than 3 months
• Not agree with the intention of this study

Trial design

100 participants in 3 patient groups

high risk group

Description:

Identified by the predictive model using 2 genotypes and disease stage

intermediate risk group

Description:

Identified by the predictive model using 2 genotypes and disease stage

Low risk group

Description:

Identified by the predictive model using 2 genotypes and disease stage