Chronic Myeloid LeukemiaPhase 2DasatinibNCT00895297
Efficacy and Safety Study of Dasatinib in Patients With Chronic Myeloid Leukemia
A Phase 2 study testing Dasatinib (Sprycel) in people with Chronic Myeloid Leukemia, run by European Society for Blood and Marrow Transplantation at 7 sites in 4 countries.
Trial summary
This is a phase II efficacy (indicates the capacity for beneficial change or therapeutic effect) and safety study of Dasatinib in patients with relapsed Chronic Myeloid Leukemia (CML) following a Stem Cell Transplant (SCT) and who are not benefiting from other treatment, such as imatinib therapy. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Chronic Myeloid Leukemia
- What is being tested?
- Dasatinib (Sprycel)
- Type of treatment
- Pill or oral medicine
- How many people
- 50 participants
- Where
- 7 sitesin 4 countries
- Study dates
- Feb 2010to Nov 2011
- Phase
- Phase 2
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Male or female patients greater or equal to 18 years of age.
- Diagnosed with BCR-ABL (+) Chronic Myeloid Leukemia (they can be Philadelphia chromosome positive or negative)
- Prior therapy including imatinib
- Patients transplanted from an HLA-identical sibling or an HLA-matched unrelated donor.
- Patients transplanted in first chronic phase or accelerated phase.
- Patients with untreated relapse of BCR-ABL (+) CML (they can be Philadelphia chromosome positive or negative) after allogeneic transplantation and entered within 6 weeks of the first detection of relapse.
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- Molecular, cytogenetic or haematological relapse in chronic or accelerated phase.
- Written informed consent.
- Absence of serious concomitant illness
Who cannot join
- Patients relapsing in blast crisis.
- Patients transplanted after blastic transformation of CML.
- Patients receiving any therapy for relapse other than withdrawal of immunosuppression (DLI is not permitted).
- Patients treated with other investigational agents during the previous 30 days
- Patients previously treated with Dasatinib.
- Absence of written informed consent.
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- Presence of serious concomitant disease.
- History of a significant bleeding disorder unrelated to CML.
- Pregnancy or lactation status positive.
- SGOT and SGPT more than 2.5 x the upper limit of the normal range as determined by the laboratory where the analysis is performed.
- Total serum bilirubin level more than 2 x the upper limit of the normal range of the laboratory where the analysis is performed.
- Serum creatinine concentration more than 1.5 x the upper limit of the normal range of the laboratory where the analysis is performed.
- Concomitant Medications, any of the following should be considered for exclusion:
- Category I drugs that are generally accepted to have a risk of causing Torsades de Points including: (Patients must discontinue drug 7 days prior to starting Dasatinib):
- quinidine, procainamide, disopyramide.
- amiodarone, sotalol, ibutilide, dofetilide.
- erythromycin, clarithromycin.
- chlorpromazine, haloperidol, mesoridazine, thioridazine, pimozide, ziprasidone.
- cisapride, bepridil, droperidol, methadone, arsenic, chloroquine, domperidone, halofantrine, levomethadyl, pentamidine, sparfloxacin, lidoflazine.
- The concomitant use of H2 blockers or proton pump inhibitors with Dasatinib is not recommended. The use of antacids should be considered in place of H2 blockers or proton pump inhibitors in patients receiving Dasatinib therapy. If antacid therapy is needed, the antacid dose should be administered at least 2 hours prior to or 2 hours after the dose of Dasatinib.
Trial locations and contacts
7 sites in 4 countries.
7 sites in 4 countries
Germany3 sites
University Hospital
Hamburg
Uniklinik Leipzig
Leipzig
Stiftung Deutsche Klinik für Diagnostik
Wiesbaden
Switzerland2 sites
University Hospital
Basel, 4031
Hopitaux Universitaires de Geneve
Geneva
About this study
Official title: Phase II Efficacy and Safety Study of Dasatinib in Patients With Chronic and Accelerated Phase Chronic Myeloid Leukemia Relapsing After Allogeneic Blood or Bone Marrow Transplantation
This is a phase II efficacy (indicates the capacity for beneficial change or therapeutic effect) and safety study of Dasatinib in patients with relapsed Chronic Myeloid Leukemia (CML) following a Stem Cell Transplant (SCT) and who are not benefiting from other treatment, such as imatinib therapy.
A relapse is when an illness that has seemed to be getting better, or to have been cured, comes back or gets worse again.
A total of 50 patients ≥18 years of age will be registered on the trial.
Read the detailed description
Primary Objective:
- To assess the efficacy of Dasatinib therapy in chronic and accelerated phase BCR-ABL (+) (Ph + and Ph -) CML patients that undergo molecular, cytogenetic or haematological relapse following SCT.
Secondary Objective(s):
- To assess the impact of Dasatinib therapy on patient survival after relapse post-SCT and the incidence of any subsequent need for 'rescue' DLI.
- To assess the safety of Dasatinib in this clinical context using this specific dose regimen
Chronic myeloid leukaemia (CML) is a form of cancer that starts in cells within the bone marrow called haematopoietic stem cells. Stem cells are immature cells which can divide many times and eventually produce all the lymphocytes and myeloid cells present in the blood. They are produced in the bone marrow - the spongy tissue found in large bones, including the pelvis, sternum, limb bones and the ribs.
Leukaemia is a cancer of the white blood cells. In CML, too many myeloid cells (one of the main types of white blood cells which defend the body against infectious diseases) are produced. The myeloid cells are released into the blood when they are immature and unable to work properly. These immature white blood cells are known as blasts.
The immature cells fill up the bone marrow and prevent it from making blood cells properly. As the leukaemia cells do not mature, they can't do the work of normal white blood cells, which leads to an increased risk of infection. Because the bone marrow is overcrowded with immature white cells it also can't make enough healthy red cells and platelets.
CML usually develops very slowly, which is why it is called 'chronic' myeloid leukaemia.
The aim of this study is to assess the efficacy (indicates the capacity for beneficial change or therapeutic effect) of a leukaemia treatment called dasatinib (sprycel) in patients with relapsed Chronic Myeloid Leukaemia (CML) following a Stem Cell Transplant (SCT) and who are not benefiting from other treatment, such as imatinib therapy.
A relapse is when an illness that has seemed to be getting better, or to have been cured, comes back or gets worse again.
Dasatinib works by blocking (inhibiting) signals within cancer cells that cause the cell to grow and divide.
The growth of cells in our bodies is controlled by signals that switch on and off within the cells. When the signals for growth are switched on the cells are triggered to grow and multiply. People with CML have an abnormal signaling protein inside their leukaemia cells. This abnormal protein sends out grow-and-divide signals to the cells at all times and never switches off.
Dasatinib finds the faulty protein and locks onto it. This prevents the protein from stimulating the cells to grow. Dasatinib is known as a signal transduction inhibitor, because it blocks the 'grow' signal. The chemical it blocks is called tyrosine kinase, so dasatinib is also known as a tyrosine kinase inhibitor.
- Conditions
- Chronic Myeloid Leukemia
- Being tested
- Dasatinib (Sprycel)
- Keywords
- Relapsing after allogeneic transplantation, Dasatinib, Sprycel, Philadelphia Chromosomes
- Medical subject headings
- Leukemia, Myelogenous, Chronic, BCR-ABL Positive
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Dasatinib (Sprycel)Drug
100mg of Dasatinib will be administered as tablets, by mouth, once a day (or twice in some cases depending on the stage of the disease) consistently either in the morning or evening for 12 months. Dose of Dasatinib will be modified according to the patients response.
What is being measured
The primary outcome is the main question the study is designed to answer.
CMR as determined by two consecutive (-) RT-PCR tests for the presence of BCR-ABL transcripts in peripheral blood samples 1 year after starting Dasatinib therapy. The expected CMR of >30% would be regarded as being clinically relevant
Measured: 4 years
Secondary outcomes (8)
Complete haematological response (CHR) at 3 months post commencing Dasatinib for those that have relapsed at the haematological level.
Measured: 4 years
Complete cytogenetic response (CCyR) at 6 and 12 months post commencing Dasatinib for those that have relapsed at the cytogenetic level.
Measured: 4 years
Major molecular response (MMR) at 12 months post commencing Dasatinib for all patients.
Measured: 4 years
Proportion of patients requiring DLI during the first 12 months
Measured: 4 years
Overall survival (OS) - Limited to 3 years.
Measured: 4 years
Progression free survival (PFS).
Measured: 4 years
Adverse event (AE) rate.
Measured: 4 years
Rate of dose reductions, interruptions and discontinuations.
Measured: 4 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted8 May 2009 (estimated)
- Study startFeb 2010
- Primary completionOct 2011
- Study completionNov 2011
Why it stopped: Slow recruitment. No safety concerns during this study.
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Chronic Myeloid LeukemiaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 50 participants (estimated)
Sponsor and investigators
- Lead sponsor
- European Society for Blood and Marrow Transplantation
- Sponsor type
- Research network
- Collaborators
- Bristol-Myers Squibb
- Investigators
- Eduardo L Olavarria, Dr, Principal investigator, Hospital De Navarra Irunlarrea, Spain
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00895297
- Sponsor's protocol ID
- 2008-001361-29
- Other IDs
- CLWP-001-2008, 2008
- Acronym
- Dasatinib
- Status last verified
- Dec 2011
- First submitted
- 6 May 2009
- Last updated
- 7 Dec 2011
- Results posted
- No
- Data monitoring committee
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 7 Dec 2011. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Phase II Efficacy and Safety Study of Dasatinib in Patients With Chronic and Accelerated Phase Chronic Myeloid Leukemia Relapsing After Allogeneic Blood or Bone Marrow Transplantation
- ClinicalTrials.gov ID
- NCT00895297
- Acronym / sponsor ID
- Dasatinib / 2008-001361-29
- Conditions
- Chronic Myeloid Leukemia
- Keywords
- Relapsing after allogeneic transplantation, Dasatinib, Sprycel, Philadelphia Chromosomes
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- TerminatedReason stopped: Slow recruitment. No safety concerns during this study.
- Enrolment
- 50 participants (estimated)
- Lead sponsor
- European Society for Blood and Marrow TransplantationResearch network
- Collaborators
- Bristol-Myers Squibb
- Study start
- Feb 2010
- Primary completion
- Oct 2011 (actual)
- Study completion
- Nov 2011 (actual)
- First posted
- 8 May 2009 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This is a phase II efficacy (indicates the capacity for beneficial change or therapeutic effect) and safety study of Dasatinib in patients with relapsed Chronic Myeloid Leukemia (CML) following a Stem Cell Transplant (SCT) and who are not benefiting from other treatment, such as imatinib therapy.
A relapse is when an illness that has seemed to be getting better, or to have been cured, comes back or gets worse again.
A total of 50 patients ≥18 years of age will be registered on the trial.
Detailed description
Primary Objective:
- To assess the efficacy of Dasatinib therapy in chronic and accelerated phase BCR-ABL (+) (Ph + and Ph -) CML patients that undergo molecular, cytogenetic or haematological relapse following SCT.
Secondary Objective(s):
- To assess the impact of Dasatinib therapy on patient survival after relapse post-SCT and the incidence of any subsequent need for 'rescue' DLI.
- To assess the safety of Dasatinib in this clinical context using this specific dose regimen
Chronic myeloid leukaemia (CML) is a form of cancer that starts in cells within the bone marrow called haematopoietic stem cells. Stem cells are immature cells which can divide many times and eventually produce all the lymphocytes and myeloid cells present in the blood. They are produced in the bone marrow - the spongy tissue found in large bones, including the pelvis, sternum, limb bones and the ribs.
Leukaemia is a cancer of the white blood cells. In CML, too many myeloid cells (one of the main types of white blood cells which defend the body against infectious diseases) are produced. The myeloid cells are released into the blood when they are immature and unable to work properly. These immature white blood cells are known as blasts.
The immature cells fill up the bone marrow and prevent it from making blood cells properly. As the leukaemia cells do not mature, they can't do the work of normal white blood cells, which leads to an increased risk of infection. Because the bone marrow is overcrowded with immature white cells it also can't make enough healthy red cells and platelets.
CML usually develops very slowly, which is why it is called 'chronic' myeloid leukaemia.
The aim of this study is to assess the efficacy (indicates the capacity for beneficial change or therapeutic effect) of a leukaemia treatment called dasatinib (sprycel) in patients with relapsed Chronic Myeloid Leukaemia (CML) following a Stem Cell Transplant (SCT) and who are not benefiting from other treatment, such as imatinib therapy.
A relapse is when an illness that has seemed to be getting better, or to have been cured, comes back or gets worse again.
Dasatinib works by blocking (inhibiting) signals within cancer cells that cause the cell to grow and divide.
The growth of cells in our bodies is controlled by signals that switch on and off within the cells. When the signals for growth are switched on the cells are triggered to grow and multiply. People with CML have an abnormal signaling protein inside their leukaemia cells. This abnormal protein sends out grow-and-divide signals to the cells at all times and never switches off.
Dasatinib finds the faulty protein and locks onto it. This prevents the protein from stimulating the cells to grow. Dasatinib is known as a signal transduction inhibitor, because it blocks the 'grow' signal. The chemical it blocks is called tyrosine kinase, so dasatinib is also known as a tyrosine kinase inhibitor.
Study design
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Single group
- Masking
- None (open label)
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (9 listed)
- Male or female patients greater or equal to 18 years of age.
- Diagnosed with BCR-ABL (+) Chronic Myeloid Leukemia (they can be Philadelphia chromosome positive or negative)
- Prior therapy including imatinib
- Patients transplanted from an HLA-identical sibling or an HLA-matched unrelated donor.
- Patients transplanted in first chronic phase or accelerated phase.
Key exclusion criteria (20 listed)
- Patients relapsing in blast crisis.
- Patients transplanted after blastic transformation of CML.
- Patients receiving any therapy for relapse other than withdrawal of immunosuppression (DLI is not permitted).
- Patients treated with other investigational agents during the previous 30 days
- Patients previously treated with Dasatinib.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Dasatinib (Sprycel)100mg of Dasatinib will be administered as tablets, by mouth, once a day (or twice in some cases depending on the stage of the disease) consistently either in the morning or evening for 12 months. Dose of Dasatinib will be modified according to the patients response. | Drug | – |
Primary outcome
CMR as determined by two consecutive (-) RT-PCR tests for the presence of BCR-ABL transcripts in peripheral blood samples 1 year after starting Dasatinib therapy. The expected CMR of >30% would be regarded as being clinically relevant
Time frame: 4 years
8 secondary outcomes
Complete haematological response (CHR) at 3 months post commencing Dasatinib for those that have relapsed at the haematological level.
Time frame: 4 years
Complete cytogenetic response (CCyR) at 6 and 12 months post commencing Dasatinib for those that have relapsed at the cytogenetic level.
Time frame: 4 years
Major molecular response (MMR) at 12 months post commencing Dasatinib for all patients.
Time frame: 4 years
Proportion of patients requiring DLI during the first 12 months
Time frame: 4 years
Overall survival (OS) - Limited to 3 years.
Time frame: 4 years
Progression free survival (PFS).
Time frame: 4 years
Adverse event (AE) rate.
Time frame: 4 years
Rate of dose reductions, interruptions and discontinuations.
Time frame: 4 years
Results and safety
The study was stopped early (reason given: Slow recruitment. No safety concerns during this study.). Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 7 Dec 2011.
- Sponsor websiteLink provided by the sponsor.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Eduardo L Olavarria, Dr principal investigator
Hospital De Navarra Irunlarrea, Spain
7 sites in 4 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing Dasatinib (Sprycel) in people with Chronic Myeloid Leukemia, run by European Society for Blood and Marrow Transplantation at 7 sites in 4 countries.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 9 inclusion and 20 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: stopped early, as of the sponsor's last update on 7 Dec 2011. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 7 sites in Germany, Switzerland, France, United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study was stopped early (reason given: Slow recruitment. No safety concerns during this study.). Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
CMR as determined by two consecutive (-) RT-PCR tests for the presence of BCR-ABL transcripts in peripheral blood samples 1 year after starting Dasatinib therapy. The expected CMR of >30% would be regarded as being clinically relevant (time frame: 4 years). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 7 Dec 2011.