Chronic Myeloid Leukemia, Philadelphia Chromosome Positive CML
Conditions
Brief summary
The purpose of this pilot study is to investigate whether some patients who were started on a 2G-TKI as first-line treatment can be safely switched to imatinib, a first-generation TKI, while maintaining or even deepening the molecular response as a cost-effective treatment. Eligible patients will be switched to imatinib 400mg daily, with regular molecular monitoring.
Detailed description
Imatinib, nilotinib and dasatinib are standard first-line options for newly diagnosed patients with chronic-phase chronic myeloid leukemia (CML). While nilotinib and dasatinib, also known as second-generation TKI (2G-TKI), have been shown to result in earlier and deeper molecular response, they have not been proven superior to imatinib in terms of clinical outcomes like progression-free survival and overall survival. Moreover, their long-term safety has been questioned: nilotinib is associated with increased cardiovascular risk while dasatinib causes pleural effusion in significant proportion of patients and may even lead to pulmonary hypertension. The purpose of this pilot study is to investigate whether some patients who were started on a 2G-TKI as first-line treatment can be safely switched to imatinib, a first-generation TKI, while maintaining or even deepening the molecular response as a cost-effective treatment. Eligible patients will be switched to imatinib 400mg daily, with regular molecular monitoring. In case of molecular progression The following should be systematically performed: * Clinical examination * Baseline blood test including complete blood count (CBC), liver and renal function, lactate dehydrogenase (LDH), urate * Restart the original 2G-TKI and in same dose as given before study entry unless medically indicated to change therapy * Screening of breakpoint cluster region- Abelson murine leukemia (BCR-ABL) kinase domain mutations * In the absence of signs of haematological relapse or breakpoint cluster region- Abelson murine leukemia (BCR-ABL1) ≥ 1% (IS ratio), bone marrow aspiration and cytogenetics are not routinely performed unless deemed indicated by the physician in charge. The patient will be followed until major molecular response (MMR) is re-achieved and further 6 months beyond. Date of progression, hematological data at progression (molecular, cytogenetic, and hematological), and treatment proposed for molecular progression and response to it (molecular, cytogenetic, hematological) will be collected. Follow-up for overall survival (OS) and progression-free survival (PFS) will last 2 years since the date of switch of TKI. In case of loss of complete hematological response (CHR) or any sign of accelerated or blastic phase of CML, the patient will be immediately considered as in disease progression and TKI should be started immediately.
Interventions
DRUGImatinib Mesylate
a first-generation tyrosine kinase inhibitors
Sponsors
The University of Hong Kong
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Adult (aged 18 years or above) patients diagnosed with chronic-phase CML 2. Must have received a 2G-TKI (nilotinib or dasatinib) as first-line therapy for at least 12 months (Note: Cytoreductive agents, namely hydroxyurea and anagrelide, prior to the use of TKI are allowed.) 3. In sustained, good molecular response (i.e. molecular response (MR3) or below) for at least 6 months, as confirmed with at least 2 consecutive quantitative real time-polymerase chain reaction (RT-PCR) results
Exclusion criteria
1. Under 18 years old 2. Adults under law protection or without ability to consent 3. Previous or planned autologous/allogeneic haematopoietic stem cell transplantation 4. Documented kinase domain mutation 5. A change to the current TKI because of unsatisfactory response to a previous TKI (Note: patients are still considered eligible if the switch in TKI was due to intolerance or side effects) 6. History of disease progression (accelerated or blast phase) 7. Patients who can speak neither Chinese nor English 8. Any molecular result during the preceding 6 months that is higher than MR3, i.e. BCR-ABL1/ABL1 ratio \>0.1% on IS ratio
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| molecular progression-free survival | 6 months | Molecular progression-free survival after switch to imatinib at 6 months |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Molecular responses | 12 months | Molecular responses after switch to imatinib at 12 months |
| molecular progression-free survival | 12 months | Molecular progression-free survival after switch to imatinib at 12 months |
| Rate of molecular progression on Imatinib | 24 months | Number of patients who have molecular progression on Imatinib |
| Rate of regain MMR after resumption of original TKI and time to recovery of MMR | 24 months | Number of patients who regain MMR on resumption of their original TKI, and time to recovery of MMR |
Countries
Hong Kong
Contacts
Primary ContactCarol Cheung, MBBS
Backup ContactCrosby Lu, MMedSc
Outcome results
None listed