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A phase II study of antithymocyte globulin in patients undergoing HLA-matched allogeneic peripheral blood stem cell transplantatio

Not Applicable
Conditions
AML,ALL,HL,NH
Registration Number
JPRN-UMIN000018645
Lead Sponsor
JSCT
Brief Summary

ow-dose ATG as a GVHD prophylaxis showed safety and efficacy for the prevention of both acute and chronic GVHD in HLA-matched PBSCT using myeloablative conditioning.

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
77
Inclusion Criteria

Not provided

Exclusion Criteria

1. Patients who are positive for HIV antibody. 2. Patients with active other malignancies. 3. Patients with active infectious disease. 4. Women who are pregnant, of childbearing potential, or lactating. 5. Patients who experienced serious hypersensitivity or anaphylaxis to antithymocyte globulin. 6. Patients who has a prior history of allogeneic transplantation. 7. Patients who are not eligible for this study at the discretion of the investigator.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The incidence of grade III-IV acute GVHD at 100 days
Secondary Outcome Measures
NameTimeMethod
1. Engraftment at 100 days. 2. The incidence of acute GVHD and chronic GVHD at 100 days, 1 year, and 2 years. 3. Non-relapse mortality at 100 days, 1 year, and 2 years. 4. The incidence of relapse at 100 days, 1 year, and 2 years. 5. Disease-free survival at 100 days, 1 year, and 2 years. 6. Overall survival at 100 days, 1 year, and 2 years. 7. The incidence of infectious event at 100 days, 1 year, and 2 years. 8. GVHD free, relapse free survival (GRFS) at 100 days, 1 year, and 2 years. 9. The proportion of patients who stopped immunosuppressive drugs within 1 year and 2 year. 10. Grade 3-4 non-hematologic toxicity within 100 days. 11. Subgroup analysis subgroup analysis according to conditioning regimen. 12. Subgroup analysis subgroup analysis according to disease risk index (DRI)
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