Graft Versus Host Disease
Conditions
Keywords
Stem cell transplantation, GVHD, Graft Versus Host Disease
Brief summary
Alefacept (AMEVIVE®) is an immunosuppressive dimeric fusion protein. It was shown to interfere with lymphocyte activation by specifically binding to the lymphocyte antigen, CD2, and inhibiting LFA-3/CD2 interaction. Alefacept was evaluated in two randomized, double-blind, placebo-controlled studies in adults with chronic (\>1 year) plaque psoriasis and a minimum body surface area involvement of 10% who were candidates for or had previously received systemic therapy or phototherapy. The response to alefacept was significantly better in both studies. In both studies, onset of response to alefacept treatment (defined as at least 50% reduction of baseline Psoriasis Area and Severity Index (PASI)) began 60 days after the start of therapy. Graft versus host disease (GVHD) is the most ominous side effect of allogeneic stem cell transplantation (SCT). It causes severe inflammatory process, which is usually located to the skin, gut and liver. Treatment of GVHD consists of various immuno-suppressive and immuno-modulating drugs, including steroids, cyclosporine, tacrolimus, methotrexate etc. These drugs unfortunately can also cause severe immunologic failure that makes the patient prone to infection and malignancy, and other medication-specific side effects. In spite of this effect on the immune system, not all of the patients achieve control of GVHD, which usually rapidly leads to death. Despite the use of innovative immunosuppressive modalities, the prognosis of steroid resistant GVHD is usually poor. It was shown that CD2 depletion of allografts could prevent GVHD. Alefacept was never systemically tried in GVHD but A phase II study of BTI-322, a rat monoclonal IgG2b directed against the CD2 antigen in steroid-refractory acute GVHD showed a total response rate of 55%. We showed that alefacept might have a beneficial effect in controlling steroid resistant aGVHD and chronic GVHD. It was also shown to dramatically change the nature of transfusion associated GVHD.
Interventions
DRUGAlefacept (AMEVIVE®)
Alefacept
DRUGcontrol group
these patients will receive the same treatment as group A, without alefacept
Sponsors
Hadassah Medical Organization
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Caregiver)
Eligibility
Sex/Gender
ALL
Age
14 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
1. Patient age 14-75 years old with a disease necessitating allogeneic SCT. 2. In order to increase security, only full matched donors will be allowed and must be willing and capable of donating peripheral blood stem cells preferably, or bone marrow progenitor cells using conventional techniques, and lymphocytes if indicated. 3. Patients must sign written informed consents. 4. Patients must have an ECOG PS ≤ 2; creatinine \< 2.0 mg/dl; ejection fraction \> 40%; DLCO \> 50% of predicted; serum bilirubin \< 3 gm/dl; elevated GPT or GOT \> 3 x normal values.
Exclusion criteria
1. Not fulfilling any of the inclusion criteria. 2. Active life-threatening infection. 3. Overt untreated infection. 4. Hypersensitivity to alefacept. 5. HIV seropositivity, Hepatitis B or C antigen positivity with active hepatitis. 6. Pregnant or lactating women. 7. Donor contraindication (HIV seropositive confirmed by western blot). 8. Hepatitis B antigenemia. 9. Evidence of bone marrow disease. 10. Unable to donate bone marrow or peripheral blood due to concurrent medical condition. 11. Inability to comply with study requirements.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Acute GVHD occurrence. | 100d |
| Acute GVHD grading. | 100d |
Secondary
| Measure | Time frame |
|---|---|
| Time to acute GVHD. | 100d |
| Chronic GVHD occurrence. | 180d |
| Chronic GVHD grading. | 180d |
| Engraftment/graft rejection. | 21d |
| Overall survival. | 180d |
| Disease free survival. | 180d |
| Infections. | 180d |
| Transplant-related mortality (TRM). | 180d |
| Immune reconstitution | 180d |
| Toxicity assessment according to the Common Terminology Criteria for Adverse Events (CTCAE) | 180d |
Countries
Israel
Outcome results
None listed