Phase
Condition
Chronic Myeloid Leukemia
Platelet Disorders
Leukemia
Treatment
Imatinib Mesylate, Dasatinib, Nilotinib or Bosutinib Withdrawal
Imatinib Mesylate, Dasatinib, Nilotinib or Bosutinib Re-initiation
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria
Patients who are 18 years or older
Patients have a diagnosis of Philadelphia chromosome- or BCR-ABL1-positive CML (as determined by cytogenetics, FISH, or PCR).
Prior evidence of a quantifiable BCR-ABL1 transcript by RT-PCR
Patients who have been taking TKI for > 36 months.
Patients must have a history of stable molecular response, defined as MR4.5 for ≥24 months, as documented by ≥3 separate tests performed at least three months apart.
Patient must have a current status of complete molecular remission (CMR), defined as MR4.5 (per section 5.1), within 30 days of signing consent.
ECOG performance status < 2
Patients must have normal marrow function within 30 days of registration, as defined:
Absolute Neutrophil Count (ANC) ≥ 1.5 x 10E9/L
Hemoglobin ≥ 9.0 g/dL
Platelets ≥ 100 x 10E9/L
Patients must not have any signs of extramedullary leukemia
Patients must have a life expectancy of more than 12 months in the absence of any intervention
All participants must be informed of the investigational nature of this study and must sign and give written informed consent
Contraception requirements will be as per routine clinical practice.
Exclusion Criteria
Patients who are unable or unwilling to give their consent to participate to the study.
Previous or planned allogeneic stem cell transplantation
Patients who have pathologies or treatments that are able to enhance the potential relapse risk after stopping Imatinib.
Patient has received an investigational agent within last 2 years
Atypical BCR-ABL transcript not quantifiable by standard RQ-PCR.
Patient cannot have had a known interruption of TKI therapy of greater than 14 consecutive days or for a total of 6 weeks in the six months prior to registration.
Another primary malignant disease, except those that do not currently require treatment (adequately treated conditions, such as excised skin cancer or cervical intra-epithelial neoplasia would not be considered exclusion criteria. If in doubt, please refer to the Principal Investigator).
Any medical condition that, in the opinion of the investigator, would exclude the patient from participating in this study.
Active liver disease (e.g., chronic active hepatitis, cirrhosis).
Known diagnosis of human immunodeficiency virus (HIV) infection.
Study Design
Study Description
Connect with a study center
Baylor College of Medicine- McNair Campus
Houston, Texas 77030
United StatesActive - Recruiting
Ben Taub General Hospital
Houston, Texas 77030
United StatesSite Not Available
CHI St. Luke's Health Baylor College of Medicine Medical Center
Houston, Texas 77030
United StatesActive - Recruiting
Harris Health System- Smith Clinic
Houston, Texas 77054
United StatesActive - Recruiting
Baylor College of Medicine- McNair Campus
Houston 4699066, Texas 4736286 77030
United StatesActive - Recruiting
Ben Taub General Hospital
Houston 4699066, Texas 4736286 77030
United StatesActive - Recruiting
CHI St. Luke's Health Baylor College of Medicine Medical Center
Houston 4699066, Texas 4736286 77030
United StatesActive - Recruiting
Harris Health System- Smith Clinic
Houston 4699066, Texas 4736286 77054
United StatesActive - Recruiting

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