Leukemia drug holiday: study tests if patients can pause treatment
NCT ID NCT04626024
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether people with chronic myeloid leukemia (CML) who have had a stable, deep response to treatment for at least two years can safely stop taking their daily targeted therapy (TKI). It involves 17 adults who have been on TKI for over three years. The main goal is to see how many remain relapse-free six months after stopping the drug.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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17 people
The number who actually took part.
- Started
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Dec 2020
- Expected to finish
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Nov 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria 1. Patients who are 18 years or older 2. Patients have a diagnosis of Philadelphia chromosome- or BCR-ABL1-positive CML (as determined by cytogenetics, FISH, or PCR). 3. Prior evidence of a quantifiable BCR-ABL1 transcript by RT-PCR 4. Patients who have been taking TKI for \> 36 months. 5. 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. 6. 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. 7. ECOG performance status \< 2 8. 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 9. Patients must not have any signs of extramedullary leukemia 10. Patients must have a life expectancy of more than 12 months in the absence of any intervention 11. All participants must be informed of the investigational nature of this study and must sign and give written informed consent 12. Contraception requirements will be as per routine clinical practice. Exclusion Criteria 1. Patients who are unable or unwilling to give their consent to participate to the study. 2. Previous or planned allogeneic stem cell transplantation 3. Patients who have pathologies or treatments that are able to enhance the potential relapse risk after stopping Imatinib. 4. Patient has received an investigational agent within last 2 years 5. Atypical BCR-ABL transcript not quantifiable by standard RQ-PCR. 6. 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. 7. 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). 8. Any medical condition that, in the opinion of the investigator, would exclude the patient from participating in this study. 9. Active liver disease (e.g., chronic active hepatitis, cirrhosis). 10. Known diagnosis of human immunodeficiency virus (HIV) infection.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Baylor College of Medicine- McNair Campus
Houston, Texas, 77030, United States
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Ben Taub General Hospital
Houston, Texas, 77030, United States
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CHI St. Luke's Health Baylor College of Medicine Medical Center
Houston, Texas, 77030, United States
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Harris Health System- Smith Clinic
Houston, Texas, 77054, United States
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Other studies related to the condition(s) this trial covers.
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- Can a smart tool keep watch on leukemia after treatment stops?