Recruitment

Recruitment Status
Active, not recruiting
Estimated Enrollment
152

Summary

Conditions
  • Acute Myeloid Leukemia
  • Chronic Myelomonocytic Leukemia
  • Myelodysplastic Syndrome
Type
Interventional
Phase
Phase 2
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: Triple (Participant, Care Provider, Investigator)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

This trial can be divided into four phases: 1) Pre-Transplant; 2) Allogeneic Transplant; 3) Vaccination; and 4) Post-Vaccination Follow-Up. Phase 1: Pre-Transplant After signing the consent form you will undergo some screening tests to find out if you can be in this research study. These tests inclu...

This trial can be divided into four phases: 1) Pre-Transplant; 2) Allogeneic Transplant; 3) Vaccination; and 4) Post-Vaccination Follow-Up. Phase 1: Pre-Transplant After signing the consent form you will undergo some screening tests to find out if you can be in this research study. These tests include a medical history, physical examination, performance status, bone marrow aspirate and biopsy, blood tests, tuberculosis skin test, HLA antibody test, pregnancy test, urine test, ECHO, MUGA or RVG to measure heart function, chest x-ray, pulmonary function tests and dental consult. If these tests show that you are eligible to participate in the research study, you will be enrolled on the trial and randomized to receive either the GVAX vaccine or the placebo vaccine after your transplant. After enrolling in the study you will undergo additional research procedures including a blood draw and leukemia cell collection. Phase 2: Allogeneic Transplant The transplant phase of the study will begin when you are admitted to the hospital to receive the chemotherapy and stem cell transplant. In the week before you receive the stem cells, you will be treated with chemotherapy. The combination of chemotherapy given before the donor cells are infused is called the conditioning regimen. The chemotherapy conditioning is given to suppress your immune system so that the donor blood stem cells will not be rejected after transplantation. The chemotherapy may also reduce the number of MDS/CMML/AML cancer cells in your body. In this study the condition regimen will include 2 chemotherapy drugs: busulfan (twice a day or four times a day for 4 days) and fludarabine (once daily for 4 days). Depending on your age and other clinical factors, your transplant doctor will decide whether you receive a higher or lower dose of busulfan. Between 1-2 days after you finish the chemotherapy, you will receive the blood stem cell or marrow from your donor. This is given as a transfusion through a central intravenous line (IV usually placed in your chest or arm). Just prior to and immediately following the infusion of stem cells, you will receive medications to help prevent graft-versus-host disease (GVHD), a common complication of transplant where your donor's immune cells attack your body. The medications you will receive to prevent GVHD will include Tacrolimus and Methotrexate. You will be closely monitored as per standard transplant care after your stem cell transplant. If you received the higher dose chemotherapy conditioning, you will stay in the hospital for an average of about 3-4 weeks. If you received the lower dose conditioning transplant, your hospital admission for transplant may be shorter depending on your clinical condition. After your stem cell infusion, you may receive daily injections of a medication called rhGM-CSF, or Leukine, to help your white blood cells to recover faster. You may receive this medication for up to 2 weeks. You will also be given antiviral and antibiotic medications to prevent infections as per standard practice after transplantation. Between 20 to 30 days after your stem cell infusion you will have a physical examination, routine blood work and a blood draw for future immune tests. Between 30 to 60 days after your transplant you will return to clinic for a visit that will include a physical examination, routine blood work, a blood draw for future immune tests and a bone marrow biopsy and aspirate to assess your MDS/CMML/AML. Phase 3: Vaccination You may begin receiving the GVAX or placebo vaccination between 30 to 60 days following your transplant, provided your blood counts have recovered, and you do not have any severe side effects from the transplant. If by day 61, your blood counts have not recovered sufficiently, or if you have developed side effects or GVHD from the transplant, and do not meet the conditions necessary to start the vaccination portion of this trial, then you will not receive any vaccinations and you will be removed from the study. You will continue to receive standard post transplant care. If you are able to begin the vaccinations between day 30-60 after your transplant, the GVAX or placebo vaccine will be administered as an injection under and into the skin on your forearms or thighs, 6 times over a period of 9 weeks. The first 3 vaccinations will be administered once a week for 3 consecutive weeks and the last 3 vaccines will be given once every other week over 6 weeks. All vaccinations will be given either as an inpatient or outpatient in the clinic. On the days you are receiving vaccination, you may have to wait several hours in the clinic while the laboratory makes final preparations on the vaccine/placebo. During this 9 week period of vaccination, you will continue to be followed by your doctor at least on a weekly basis to monitor for any transplant or possible vaccine side effects.Two to three days after the first and fifth vaccinations, we would encourage you (but do not require you) to return to the clinic to have a skin biopsy of the GVAX/Placebo vaccination site, especially if there is redness or swelling in the area. This will allow researchers to assess whether your new immune system is reacting to the injected leukemia cells under the microscope. During the course of the study, we will also be drawing your blood on a regular basis to evaluate immune cells and the effect that the vaccinations may have on your new immune system. If you tolerate the vaccinations well, and do not have GVHD or any severe side effects from the transplant or the vaccinations, you will complete a total of 6 vaccines. However, your vaccination may be terminated earlier if you develop any side effects (from transplant or vaccination) that do not resolve/improve after 2 weeks, if you develop GVHD that requires steroid treatment, or if your MDS/CMML/AML relapses and you need to receive more treatment. Phase 4: Post Vaccination Follow-UP About 1 month after your last vaccination, you will have a physical examination, blood work, immune bloods and bone marrow biopsy and aspirate to assess the status of your disease. You will be followed at an appointment 6, 9, 12 and 18 months following your transplant with physical examinations, blood work and immune bloods. At the 12 and 18 month visit you will have a bone marrow biopsy and aspirate to assess the status of your AMLCMML//MDS.

Tracking Information

NCT #
NCT01773395
Collaborators
  • Massachusetts General Hospital
  • Beth Israel Deaconess Medical Center
Investigators
Principal Investigator: Vincent Ho, MD Dana-Farber Cancer Institute