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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.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
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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

Other trials in Germany

Switzerland2 sites
  • University Hospital

    Basel, 4031

  • Hopitaux Universitaires de Geneve

    Geneva

Other trials in Switzerland

France1 site
  • E Herriot Hospital

    Lyon

Other trials in France

United Kingdom1 site
  • Hammersmith Hospital

    London, W12 0NN

Other trials in United Kingdom

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:

  1. 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):

  1. To assess the impact of Dasatinib therapy on patient survival after relapse post-SCT and the incidence of any subsequent need for 'rescue' DLI.
  2. 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.

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.

  1. 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)
  1. Complete haematological response (CHR) at 3 months post commencing Dasatinib for those that have relapsed at the haematological level.

    Measured: 4 years

  2. Complete cytogenetic response (CCyR) at 6 and 12 months post commencing Dasatinib for those that have relapsed at the cytogenetic level.

    Measured: 4 years

  3. Major molecular response (MMR) at 12 months post commencing Dasatinib for all patients.

    Measured: 4 years

  4. Proportion of patients requiring DLI during the first 12 months

    Measured: 4 years

  5. Overall survival (OS) - Limited to 3 years.

    Measured: 4 years

  6. Progression free survival (PFS).

    Measured: 4 years

  7. Adverse event (AE) rate.

    Measured: 4 years

  8. 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.

  1. First posted8 May 2009 (estimated)
  2. Study startFeb 2010
  3. Primary completionOct 2011
  4. Study completionNov 2011

Why it stopped: Slow recruitment. No safety concerns during this study.

Resources

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)
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

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.

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