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Phase 2 N=25 Treatment

Low Dose IL-2, Hematopoietic Stem Cell Transplantation, IL2 for GVHD

Acute Lymphoblastic Leukemia · ALL · Acute Myelogenous Leukemia · AML · Chronic Myelogenous Leukemia

Enrolled (actual)
25
Serious AEs
45.5%
Results posted
Jul 2014
Primary outcome: Primary: Rate of Dose Limiting Toxicities — 0.045 proportion of participants of DLT

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
IL-2 (Biological)
Age
Pediatric, Adult, Older Adult
Sex
All
Sponsor
Baylor College of Medicine
Primary completion
Apr 2013

Outcome Measures

OutcomeResultp-value
PRIMARY
Rate of Dose Limiting Toxicities
0.045
SECONDARY
Rate of Severe (Grade III or IV) Acute GVHD
4.5
SECONDARY
Percentage Change in CD4+ CD25+ FoxP3+ Regulatory T Cells (Tregs) From Pre to Post IL-2 Infusions
55.6

Summary

Patients are being asked to participate in this study because treatment for their disease requires a stem cell transplant (SCT). Stem cells are the source of normal blood cells found in the bone marrow and lead to recovery of blood counts after bone marrow transplantation. With stem cell transplants, regardless of whether the donor is a full match to the patient or not, there is a risk of developing graft-versus-host disease (GVHD). GVHD is a serious and sometimes fatal side effect of SCT. GVHD occurs when the new donor stem cells (graft) recognizes that the body tissues of the patient (host) are different from those of the donor. When this happens, cells in the graft may attack the host organs. How much this happens and how severe the GVHD is depends on many things, including how different the donors cells are, the strength of the drugs given in preparation for the transplant, the quality of transplanted cells and the age of the person receiving the transplant. Typically, acute GVHD occurs in the first 100 days following transplant, while chronic GVHD occurs after day 100. Acute GVHD most often involves the skin, where it can cause anywhere from a mild rash to complete removal of skin; liver, where it can anywhere from a rise in liver function tests to liver failure; and the gut, where it can cause anywhere from mild diarrhea to profuse, life-threatening diarrhea. Most patients who develop GVHD experience a mild to moderate form, but some patients develop the severe, life-threatening form. Previous studies have shown that patients who receive SCT's can have a lower number of special T cells in their blood, called regulatory T cells, than people who have not received stem cell transplants. When regulatory T cells are low, there appears to be an increased rate of severe, acute GVHD. A drug known as IL-2 (Proleukin) has been shown to increase the number of regulatory T cells in patients following stem cell transplant, and in this study investigators plan to give low dose IL-2 after transplant. This study is called a phase II study because its major purpose is to find out whether using a low-dose of IL-2 will be effective in preventing acute GVHD. Other important purposes are to find out if this treatment helps the patient's immune system recover regulatory T cells faster after the transplant. This study will assess the safety and toxicity of low-dose IL-2 given to patients after transplantation and determine whether this drug is helpful in preventing GVHD.

Eligibility Criteria

INCLUSION CRITERIA

INCLUSION CRITERIA FOR INITIAL STUDY ENROLLMENT:

Patients will be eligible for initial enrollment on this study as long as they meet the following criteria:

  • Diagnosis of acute lymphoblastic leukemia, acute myelogenous leukemia, chronic myelogenous leukemia, myelodysplastic syndrome, myeloproliferative disorder, Hodgkin lymphoma, non-Hodgkin lymphoma or non-malignant disease requiring allogeneic HSCT
  • Birth to age 70 years of age
  • Study entry consent is signed and faxed to Research Coordinator

INCLUSION CRITERIA AT TIME OF IL-2 ADMINISTRATION:

  • At least day +7 post transplant
  • Less than or equal to 30 days post transplant
  • Lansky or Karnofsky score greater than or equal to 50%
  • Total bilirubin less than or equal to 1.5mg/dL
  • Alanine aminotransferase level (ALT) less than or equal to five times normal, serum direct bilirubin less than or equal to 1.5mg/dL, albumin greater than or equal to 3.0gm/dL
  • Serum creatinine less than three times normal or creatinine clearance greater than 80mg/min/1.73m2
  • Ensure that informed consent signed and faxed to Research Coordinator

EXCLUSION CRITERIA

EXCLUSION CRITERIA AT TIME OF IL-2 ADMINISTRATION:

Patients will be ineligible to receive IL-2 injections if any of the following is true:

  • Active, acute GVHD greater than or equal to grade II
  • Serious, active bacterial, fungal or viral infection (i.e. intensive care)
  • Clinical Signs of severe pulmonary dysfunction
  • Clinical Signs of sever cardiac dysfunction
  • Receiving corticosteroids as GVHD treatment
  • Hypersensitivity or allergy to IL-2
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00539695). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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