Abstract
The best strategies for haploidentical stem cell transplants are not known. we used a standard myeloablative pretransplant conditioning regimen (30 mg/kg vp-16, 120 mg/kg cyclophosphamide, and 12 gy of tbi in six fractions), an increased peripheral stem cell dose of >10 × 106 CD34+ cells/kg, T cell depletion (with CD34+cell selection and CD4/CD8 depletion steps) to <1 × 105 CD3+ cells/kg and cyclosporine post transplant. Ten patients (7M/3F, median age 11 (3–33) years) with high-risk leukemia (AML in 4, MDS in 2, CML in 1 and T-ALL in 3) received a hemopoietic stem cell transplant (HSCT) from a haploidentical father or sibling. The median number of CD34+ cells was 12.9 (9.5–45.7) × 106 cells/kg; median number of CD3+ cells was 0.41 (0.09–1.89) × 105 CD3+ cells/kg. All patients initially achieved 0.5 × 109/l neutrophils at a median 12 (10–21) days. graft failure in two consecutive patients out of four on the original protocol led to a modification adding atg pretransplant and okt3 post transplant. graft failure was observed in one out of six subsequent patients. acute gvhd ⩾grade ii was observed in three patients. three of 10 patients are alive in cr at >24 and >3 (2) months after transplant. Seven patients died: four of transplant related complications and three of relapse. Increased stem cell dose (⩾10 × 106 CD34+ cells/kg) as obtained using currently available technology may not be sufficient to ensure stable engraftment in patients with high-risk leukemia using standard myeloablative conditioning regimens. Bone Marrow Transplantation (2000) 26, 1033–1036.
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Passweg, J., Kühne, T., Gregor, M. et al. Increased stem cell dose, as obtained using currently available technology, may not be sufficient for engraftment of haploidentical stem cell transplants. Bone Marrow Transplant 26, 1033–1036 (2000). https://doi.org/10.1038/sj.bmt.1702669
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DOI: https://doi.org/10.1038/sj.bmt.1702669
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