Unrelated cord blood transplant experience by the pediatric blood and marrow transplant consortium

Cord blood (CB) has emerged as a potential source of hematopoietic stem cel ls for patients who are in need of hematopoietic stem cell transplant (HSCT ). The authors analyzed the Pediatric Blood and Marrow Transplant Consortiu m's (PBMTC) data of consecutive unrelated CB transplants performed during t he initial 2 years of using placental blood grafts. From January 1995 to De cember 1996 PBMTC performed a total of 44 unrelated CB transplant for a var iety of diseases consisting of acute leukemias (n = 29), congenital conditi ons (n = 9), and bone marrow failure (n = 6). There were 15 females and 29 males with median age of 5 years (range 0.4-20.6 years) and median weight o f 18.2 kg (range 6.3-70 kg). The median volume of CB units was 80 mL (range 44.5-215 mL) and the median cell dose given was 4.3 x 10(7) /kg of recipie nt weight (range 1.1-23 x 10(7) /kg). Techniques used for human leukocyte a ntigen (HLA) matching were serologic typing for class 1 HLA antigens and hi gh-resolution molecular typing for HLA-DRB1 alleles. HLA disparities were a s follows: 4 were 6/6 matches, 21 were 5/6, 15 were 4/6 and 4 were 3/6. Twe nty-nine (66 %) of CB units were DRB1 matched with recipients. Conditioning regimens consisted of either total body irradiation containing (n = 31) or chemotherapy only (n I I) regimens. All but 3 patients receive cyclosporin e as part of graft vs, host disease (GvHD) prophylaxis in combination with either methotrexate (MTX) or methylprednisolone (Pred). The other 3 patient s had FK506 and MTX for GVHD prophylaxis. Myeloid engraftment (absolute neu trophil count greater than or equal to 500) occurred at a median of 21 days (range 10-43 days) and platelet greater than or equal to 50,000/mm(3) was noted at a median of 44 days (range 16-102 days). Eight patients died too e arly (< day + 28)for evaluation of engraftment (5 for infection 2 for multi organ failure, 1 for toxic epidermolysis). The probability of having grade II-IV acute GvHD for all patients was 44 +/- 0.7 %. The incidence of a GvHD is similar for 4/6 and 5/6 antigen when DRB1 matched, at 47 and 52 %, resp ectively. Chronic GVHD was noted in 28 % of patients surviving.