ASTX727 and Dasatinib for the Treatment of Newly Diagnosed Philadelphia Chromosome or BCR-ABL Positive Chronic Myeloid Leukemia in Chronic Phase

Launched by M.D. ANDERSON CANCER CENTER · Aug 16, 2021

Keywords

ClinConnect Summary

This clinical trial is exploring the use of two medications, ASTX727 and dasatinib, to treat patients who have recently been diagnosed with a type of blood cancer called chronic myeloid leukemia (CML) that is positive for the Philadelphia chromosome or BCR-ABL mutation. These medications work in different ways to stop the growth of cancer cells and may help control the disease in its early stages.

To participate in this trial, patients should be diagnosed with Philadelphia chromosome-positive CML within the last year and should not have received much prior treatment. Other eligibility criteria include good overall health as determined by a specific performance scale and adequate organ function. Patients can expect to be monitored closely throughout the study, and those who qualify will receive these investigational treatments. It's important for potential participants to understand the nature of this study and the commitment involved, including following guidelines for contraception if applicable.

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Eligibility criteria

• Inclusion Criteria:
• • Diagnosis of Philadelphia chromosome (Ph)-positive or BCR-ABL positive CML in early chronic phase CML (i.e., time from diagnosis ≤12 months). Except for hydroxyurea and/or 1 to 2 doses of cytarabine patients must have received no or minimal prior therapy, defined as \< 1 month (30 days) of prior Food and Drug Administration (FDA) approved tyrosine kinase inhibitor (TKI)
• • Clonal evolution defined as the presence of additional chromosomal abnormalities other than the Ph chromosome has historically been included as a criterion for accelerated phase. However, patients with clonal evolution as the only criterion of accelerated phase have a significantly better prognosis, and when present at diagnosis may not impact the prognosis at all. Thus, patients with clonal evolution at diagnosis (early disease) and no other criteria for accelerated phase will be eligible for this study.
• • Eastern Cooperative Oncology Group (ECOG) performance of 0-2
• • Adequate end organ function, defined as the following: total bilirubin \<1.5x ULN (unless secondary to Gilbert's disease, in which case should be \< 2.5x ULN), SGPT \<3x ULN, creatinine clearance ≥ 30mL/min calculated using modified Crokcroft-Gault.
• • Patients must sign an informed consent indicating they are aware of the investigational nature of this study, in keeping with the policies of the hospital.
• • Males must be surgically or biologically sterile or agree to use an adequate method of contraception during the study until 3 months after the last treatment.
• Exclusion Criteria:
• • New York Heart Association (NYHA) cardiac class 3-4 heart disease
• * Cardiac Symptoms: Patients meeting the following criteria are not eligible unless cleared by Cardiology:
• • Uncontrolled angina within 3 months
• • Diagnosed or suspected congenital long QT syndrome
• • Any history of clinically significant ventricular arrhythmias (such as ventricular tachycardia, ventricular fibrillation, or Torsades de pointes).
• • Prolonged corrected QT (QTc) interval on pre-entry electrocardiogram (\> 460 msec)
• • History of significant bleeding disorder unrelated to cancer, including unless cleared by hematologist or hemato-oncologist
• • Diagnosed congenital bleeding disorders (e.g., von Willebrand's disease)
• • Diagnosed acquired bleeding disorder within one year (e.g., acquired anti-factor VIII antibodies)
• • Patients with active, uncontrolled psychiatric disorders include: psychosis, major depression, and bipolar disorders
• • Subject is known to be positive for human immunodeficiency virus (HIV) (HIV testing is not required)
• * Evidence of other clinically significant uncontrolled condition(s) including, but not limited to:
• • Uncontrolled and/or active systemic infection (viral, bacterial or fungal)
• • Chronic hepatitis B virus (HBV) or hepatitis C (HCV) requiring treatment. Note: subjects with serologic evidence of prior vaccination to HBV (i.e. hepatitis B surface \[HBs\] antigen negative-, anti-HBs antibody positive and anti-hepatitis B core \[HBc\] antibody negative) or positive anti-HBc antibody from intravenous immunoglobulins (IVIG) may participate
• • Women of pregnancy potential must practice an effective method of birth control during the course of the study, in a manner such that risk of failure is minimized. Prior to study enrollment, women of childbearing potential (WOCBP) must be advised of the importance of avoiding pregnancy during trial participation and the potential risk factors for an unintentional pregnancy. Postmenopausal women must be amenorrheic for at least 12 months to be considered of non-childbearing potential. Women must continue birth control for the duration of the trial and at least 3 months after the last dose of study drug.
• • Pregnant or breast-feeding women are excluded.
• • All WOCBP must have a negative pregnancy test prior to first receiving investigational product. If the pregnancy test is positive, the patient must not receive study drug and must not be enrolled in the study
• * Patients in late chronic phase (i.e., time from diagnosis to treatment \> 12 months), accelerated (except as noted in inclusion criteria 4.1) or blast phase are excluded. The definitions of CML phases are as follows:
• • Early chronic phase: time from diagnosis to therapy ≤ 12 months
• • Late chronic phase: time from diagnosis to therapy \> 12 months
• • Blastic phase: presence of 30% blasts or more in the peripheral blood or bone marrow
• * Accelerated phase CML: presence of any of the following features:
• • Peripheral or marrow blasts 15% or more
• • Peripheral or marrow basophils 20% or more
• • Thrombocytopenia \< 100 x 10\^9/L unrelated to therapy
• • Documented extramedullary blastic disease outside liver or spleen