This phase 2 single-arm study aims to demonstrate the efficacy of strong cytochrome inhibition with ketoconazole to reduce dasatinib dosage for adults with chronic myelogenous leukemia. Researchers will describe response rates and adverse events.
Dasatinib is a second-generation tyrosine kinase inhibitor that is metabolized by the cytochrome P450. Dasatinib has shown efficacy in patients with chronic myelogenous leukemia. Standard-dose dasatinib is 50mg-140mg/day orally, continuously. However, when combined with a strong CYP3A4 inhibitor, a dose reduction of 75% is warranted. This phase 2 single-arm study aims to demonstrate the efficacy of strong cytochrome inhibition with ketoconazole to reduce the dosage and costs of dasatinib for adults with chronic myelogenous leukemia. Researchers will describe cytogenetic and molecular response rates at 3, 6, and 12 months and adverse events (i.e., pleural effusion) associated with this strategy.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
15
Patients will receive half pill of dasatinib 50mg (25mg/day, orally) for one year
Patients will receive ketoconazole 200mg two times a day, orally, for one year.
Hospital Universitario Dr. José Eleuterio González
Monterrey, Nuevo León, Mexico
RECRUITINGThe rate of Complete Cytogenetic Response
B-cell antigen receptor(BCR)/Tyrosine-protein kinase-ABL1(ABL1) IS \<=1% at 6 months
Time frame: Up to 6 months
The rate of Molecular Response (MR4)
Log reduction in BCR/ABL of 4
Time frame: Up to 6 months
The rate of Molecular Response (MR4.5)
Log reduction in BCR/ABL of 4.5
Time frame: Up to 6 months
The rate of sustained Molecular Response (MR4.5)
Log reduction in BCR/ABL of 4.5
Time frame: Up to 12 months
The proportion of non hematological side effects
Proportion of patients that presented non hematological side effects to the intervention
Time frame: Up to 12 months
The rate of Complete Cytogenetic Response
BCR/ABL IS \<=1% at 12 months
Time frame: Up to 12 months
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