Treatment of CML Patients With Imatinib and Hydroxyurea (CML2004)

University of Leipzig

Status and phase: Completed; Phase 2; Phase 1

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

Treatments: Drug: Hydroxyurea; Drug: Imatinib

Study type: Interventional

Funder types: Other

Identifiers

NCT02480608

68

Details and patient eligibility

About

The study will test the tolerability and efficacy of the combination therapy Imatinib/Hydroxyurea (HU) in patients with chronic myeloid leukemia (CML) in first chronic phase (CP1) newly diagnosted or failing interferon-based therapy.

Full description

The protocol consists of a part 1, a phase I study that will enrol 20 patients, with the goal to determine the safety of the combination as well as the maximal tolerated dose. If the toxicity of the combination is acceptable, up to 200 more patients may be recruited and randomized to receive either Imatinib/HU or Imatinib alone (part 2).

Patients who meet the inclusion criteria will be started on 400 mg Imatinib daily. In part 1 of the protocol, the dose of HU will be increased by 500 mg at 3-weekly intervals until the maximal tolerated dose has been reached. In part 2 of the study, patients will be randomized to receive either the combination or Imatinib monotherapy.

Hematological and cytogenetic response will be evaluated at 3-months intervals during the first year, and at 6 months' intervals thereafter. Primary endpoints for part 1 are dose-limiting toxicity and maximal tolerated dose. Primary endpoints for part 2 are the rates of major and complete molecular response at 6, 12 and 18 months, respectively.

Enrollment: 113 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Ph-positive CML in CP1, newly diagnosed or resistant (hematologic or cytogenetic) or intolerant to interferon-based therapy
2. Age ≥ 18 years
3. Negative pregnancy test
4. Low- and intermediate risk patients younger than 45 with an HLA (Human Leukocyte Antigen) -matched sibling donor and medically fit to undergo allografting should be included only after they have been adequately counselled about the potential risk (of disease progression) associated with delaying the allograft
5. Informed consent

Exclusion criteria

1. Objective signs of disease progression beyond CP1 defined as

   • bone marrow or peripheral blood blasts > 15% and/or
   • blasts + promyelocytes ≥ 30% and/or
   • peripheral blood basophils ≥ 20% and/or
   • platelets < 100/nl and/or
   • chromosomal abnormalities in addition to the Ph chromosome

2. Findings suggestive of extramedullary involvement

3. Any severe and uncontrolled medical condition

4. Previous treatment with Imatinib (only part 2 of the study)

5. History of non-compliance

6. Simultaneous inclusion in other studies

Important note: previous treatment with Imatinib only is not an exclusion criterion for part 1 of the study.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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113 participants in 2 patient groups

combination Imatinib + Hydroxyurea

Experimental group

Description:

Patients who meet the inclusion criteria will be started on 400 mg Imatinib daily. In part 1 of the protocol, the dose of HU will be increased by 500 mg at 3-weekly intervals until the maximal tolerated dose has been reached. In part 2 of the study, patients will be randomized to receive either the combination or Imatinib monotherapy.

Treatment:

Drug: Imatinib

Drug: Hydroxyurea

monotherapy Imatinib

Active Comparator group

Description:

Imatinib monotherapy

Treatment:

Drug: Imatinib