LeukemiaPhase 2NCT00143884
Study of Low Intensity Conditioning and Immunotherapy for High-Risk Cancers of the Blood
A Phase 2 study testing Reduced intensity conditioning and Prophylactic donor leukocyte infusions in people with Leukemia and Lymphoma, Low-Grade, run by University of Michigan Rogel Cancer Center at 1 site in United States.
Trial summary
This research project will focus on whether it is safe and effective to rely on donor cells to prevent relapse of leukemia, lymphoma, or other blood cancer after bone marrow stem cell transplant. Read more about this study
- Who is it for?
- Any age
- Conditions the study is for
- Leukemia, Lymphoma, Low-Grade, Lymphoma, Non-Hodgkin's
- What is being tested?
- Reduced intensity conditioning and Prophylactic donor leukocyte infusions
- Type of treatment
- Injection or infusion, Surgery or procedure
- How many people
- 30 participants
- Where
- 1 siteUnited States
- Study dates
- Mar 2000to not given
- 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 Any age
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Patient Inclusion Criteria:
- One of the following hematological malignancies:
- Chronic myelogenous leukemia
- Accelerated phase
- Blast phase
- Acute myelogenous leukemia
- First or greater complete remission if high risk features: abnormalities of chromosomes with known poor prognosis 5 or 7.
- Relapsed or refractory patients with ≤ 30% blasts
- Aged 55 years or older in any disease state beyond first remission if blast percentage is < 30%.
- Acute lymphoblastic leukemia
- First complete remission if high risk features: t(4;11)
- Second complete remission if relapse occurs within the first 12 months of therapy
- Third or greater complete remission
- Relapsed or refractory patients with ≤ 30% blasts
- Aged 55 years or old in second in any disease state beyond first remission if blast percentage is < 30%.
- Myelodyplastic syndromes
- RAEB or RAEB-t patients, 55 years of age or older
- Any hematologic malignancy relapsed following autologous or matched related donor allogeneic stem cell transplant provided at least 90 days has elapsed from most recent transplant
- Non-Hodgkin's Lymphoma
- 55 years or older, who have failed anthracycline containing regimen and do not have any tumor larger than 5 cm in diameter.
- Patients with rapidly progressive disease are ineligible.
- Multiple myeloma patients, any age, who meet at least one of the following criteria:
- disease refractory to conventional chemotherapy such as VAD, pulse decadron, or alkylating agents, OR
- chromosomal abnormality by cytogenetics or FISH probe.
- Chronic lymphoblastic leukemia patients
- Any age
- Advanced disease (Rai stage 3 or 4)
- Relapsed following/refractory to alkylating agents or nucleoside analog therapy
- NOTE: Patients with bulky disease (lymphadenopathy > 5 cm) or progressive disease NOT eligible.
- Mantle cell lymphoma
- Any age
- Disease stage 3 or 4
- Lymphadenopathy must not exceed 5 cm in any dimension
- Any eligible disease category, any age, if ineligible for myeloablative conditioning because of organ dysfunction or advanced age (55 years or older). Minimum organ function for patients entered on this protocol defined as:
- Cardiac: Ejection fraction at least 30%.
- Renal: Creatinine <1.5 times normal for age.
- Pulmonary: FEV1 and FVC >60%.
- Hepatic: Total bilirubin <2.0 and AST/ALT <3 X institutional normal for age.
- Performance (adults): Karnofsky score must be at least 60; for pts. under 16, Lansky score must be at least 60.
- Low grade lymphoma (small lymphocytic, follicular small cleaved cell, or follicular mixed small cleaved and large cell) must meet the following criteria:
- any age
- relapsed or refractory disease provided the disease is NOT rapidly progressive
- no lymphoma mass or lymph node exceeds 5 cm in greatest dimension
- Age: no age restriction
- Availability of a 6/6 HLA A, B, and DR identical relative who is willing and able to donate allogeneic stem cells
- No active infection
- Serum creatinine less than 1.5 times normal for age
- Serum bilirubin less than 1.5 times normal for age
- Not pregnant.
Patient Exclusion Criteria:
- HIV positive patients not eligible
- Pregnant
Donor Inclusion Criteria:
- 6/6 HLA match for HLA-A, B, and DR
- Age 3-70 years, good general health
- No contraindication to G-CSF stimulation
- No contraindication to leukapheresis of peripheral blood stem cells
- Good general health
Donor Exclusion Criteria:
- HIV positive or history of HIV risk factors
- Presence of other diseases transmissible by blood that pose unacceptable risk to the study subject.
- Pregnant
- Medical or psychological conditions that would make the donor unlikely to tolerate G-CSF injections or leukapheresis
Trial locations and contacts
1 site in 1 country.
United States1 site
The University of Michigan
Ann Arbor, Michigan, 48109
About this study
Official title: Adjuvant Cellular Immunotherapy for High-Risk Hematologic Malignancy After Allogeneic Stem Cell Transplantation Using Low Intensity Conditioning
This research project will focus on whether it is safe and effective to rely on donor cells to prevent relapse of leukemia, lymphoma, or other blood cancer after bone marrow stem cell transplant.
Read the detailed description
This research project will focus on whether it is safe and effective to rely on donor cells to prevent relapse of leukemia, lymphoma, or other blood cancer after bone marrow stem cell transplant (SCT). For many patients with these conditions, a bone marrow transplant can be the only chance for cure. The standard type of bone marrow transplant involves giving very high-doses of chemotherapy and radiation to kill all the cancer cells followed by an infusion of bone marrow stem cells from a relative who is a bone marrow match. After the transplant the patient takes anti-rejection drugs for many months to prevent the donor's immune cells from causing a severe reaction called Graft-versus-Host Disease (GVHD), which can even be fatal. However, for some patients with certain types of high-risk cancer even this intense treatment is not effective and the cancer relapses.
Is has been known for many years that some of the bone marrow cells from the donor can kill cancer cells. Recently, it has been discovered that sometimes patients who relapse after a bone marrow SCT can be cured by giving an infusion of donor white blood cells (called a donor leukocyte infusion or DLI). By giving a DLI BEFORE a relapse happens, hopefully relapse can be prevented.
The high doses of chemotherapy and radiation therapy given prior to a standard bone marrow stem cell transplant can make a patient very sick and also increase the chance of getting severe GVHD. In this research study we are going to rely mainly on the donor cells to kill the cancer cells, and patients will receive dosages of chemotherapy that are lower than the usual dosages. It is thought that this low intensity conditioning will make the transplant safer without risking more relapses, however it is not know whether low intensity conditioning is safer than standard conditioning.
- Conditions
- Leukemia, Lymphoma, Low-Grade, Lymphoma, Non-Hodgkin's, Multiple Myeloma, Myelodysplastic Syndromes
- Being tested
- Reduced intensity conditioning, Prophylactic donor leukocyte infusions
- Medical subject headings
- Leukemia, Lymphoma, Non-Hodgkin, Multiple Myeloma, Myelodysplastic Syndromes
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Reduced intensity conditioningProcedure or surgery
Prophylactic donor leukocyte infusionsProcedure or surgery
What is being measured
The primary outcome is the main question the study is designed to answer.
To conduct a phase I-II trial of prophylactic cellular immunotherapy after allogeneic hematopoietic stem cell therapy using low intensity conditioning for high-risk hematological malignancies
Secondary outcomes (1)
To evaluate both surrogate markers of GVHD (with a cytokine panel) and minimal residual disease and correlate these with clinical outcomes during the above trial
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted2 Sep 2005 (estimated)
- Study startMar 2000
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for LeukemiaStudies of the same condition, open and under way.
- More trials run by University of Michigan Rogel Cancer CenterThe sponsor's other registered studies.
- 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
- Early clinical test
- Allocation
- Non-randomised
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 30 participants
Sponsor and investigators
- Lead sponsor
- University of Michigan Rogel Cancer Center
- Sponsor type
- University, hospital or other
- Investigators
- John E. Levine, MS MD, Principal investigator, The Univeristy of Michigan
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00143884
- Sponsor's protocol ID
- UMCC 9979
- Status last verified
- Jan 2007
- First submitted
- 31 Aug 2005
- Last updated
- 23 Apr 2007
- Results posted
- No
Study at a glance
From the registry record, last updated by the sponsor on 23 Apr 2007. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Adjuvant Cellular Immunotherapy for High-Risk Hematologic Malignancy After Allogeneic Stem Cell Transplantation Using Low Intensity Conditioning
- ClinicalTrials.gov ID
- NCT00143884
- Acronym / sponsor ID
- UMCC 9979
- Conditions
- Leukemia, Lymphoma, Low-Grade, Lymphoma, Non-Hodgkin's, Multiple Myeloma, Myelodysplastic Syndromes
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Terminated
- Enrolment
- 30 participants
- Lead sponsor
- University of Michigan Rogel Cancer CenterUniversity, hospital or other
- Study start
- Mar 2000
- First posted
- 2 Sep 2005 (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 research project will focus on whether it is safe and effective to rely on donor cells to prevent relapse of leukemia, lymphoma, or other blood cancer after bone marrow stem cell transplant.
Detailed description
This research project will focus on whether it is safe and effective to rely on donor cells to prevent relapse of leukemia, lymphoma, or other blood cancer after bone marrow stem cell transplant (SCT). For many patients with these conditions, a bone marrow transplant can be the only chance for cure. The standard type of bone marrow transplant involves giving very high-doses of chemotherapy and radiation to kill all the cancer cells followed by an infusion of bone marrow stem cells from a relative who is a bone marrow match. After the transplant the patient takes anti-rejection drugs for many months to prevent the donor's immune cells from causing a severe reaction called Graft-versus-Host Disease (GVHD), which can even be fatal. However, for some patients with certain types of high-risk cancer even this intense treatment is not effective and the cancer relapses.
Is has been known for many years that some of the bone marrow cells from the donor can kill cancer cells. Recently, it has been discovered that sometimes patients who relapse after a bone marrow SCT can be cured by giving an infusion of donor white blood cells (called a donor leukocyte infusion or DLI). By giving a DLI BEFORE a relapse happens, hopefully relapse can be prevented.
The high doses of chemotherapy and radiation therapy given prior to a standard bone marrow stem cell transplant can make a patient very sick and also increase the chance of getting severe GVHD. In this research study we are going to rely mainly on the donor cells to kill the cancer cells, and patients will receive dosages of chemotherapy that are lower than the usual dosages. It is thought that this low intensity conditioning will make the transplant safer without risking more relapses, however it is not know whether low intensity conditioning is safer than standard conditioning.
Study design
- Primary purpose
- Early clinical test
- Allocation
- Non-randomised
- Intervention model
- Single group
- Masking
- None (open label)
Who may qualify
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
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 |
|---|---|---|
| Reduced intensity conditioning | Procedure or surgery | – |
| Prophylactic donor leukocyte infusions | Procedure or surgery | – |
Primary outcome
To conduct a phase I-II trial of prophylactic cellular immunotherapy after allogeneic hematopoietic stem cell therapy using low intensity conditioning for high-risk hematological malignancies
1 secondary outcome
To evaluate both surrogate markers of GVHD (with a cytokine panel) and minimal residual disease and correlate these with clinical outcomes during the above trial
Results and safety
The study was stopped early. Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 23 Apr 2007.
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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.
John E. Levine, MS MD principal investigator
The Univeristy of Michigan
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing Reduced intensity conditioning and Prophylactic donor leukocyte infusions in people with Leukemia and Lymphoma, Low-Grade, run by University of Michigan Rogel Cancer Center at 1 site in United States.
The full registered description is in the About this study section and the official record.
Is this clinical trial currently recruiting?
The record says: stopped early, as of the sponsor's last update on 23 Apr 2007. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. 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. 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?
To conduct a phase I-II trial of prophylactic cellular immunotherapy after allogeneic hematopoietic stem cell therapy using low intensity conditioning for high-risk hematological malignancies. 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 23 Apr 2007.