Factors influencing the haematological recovery after allogeneic bone marrow transplantation in leukaemia patients treated with methotrexate-containing GVHD prophylaxis: a single-centre experience.

1997 
In the present single institution study of 66 leukaemia patients (28 AML, 23 ALL, 15 CML), the factors influencing haematological recovery after allogeneic bone marrow transplantation (alloBMT) were analysed retrospectively in order to identify the optimal conditions required for a rapid haematological recovery after alloBMT. All patients received GVHD prophylaxis with cyclosporine A plus methotrexate. The mean number of days required to achieve ≥ 0.5 x 10 9 /l neutrophil count after alloBMT was 17 (median 17, range 9 to 27 days) and 19 patients (28.8%) had rapid neutrophil recovery within 15 days after alloBmT. The haematological recovery was more rapid in the 38 patients without GVHD or with only grade I GVHD. Furthermore, 50% and 40% of patients receiving 10 (n= 18) or 5 (n=20) μg/kg/day G-CSF had rapid neutrophil recovery within 15 days after alloBmT, versus only 7.1% of patients not receiving G-CSF post-transplant (n=28), p 1 x 10 5 CFU-GM/kg (n=28) versus 19 days (median 19, range 13 to 27 days) in patients receiving allografts containing 1.0 x 10 5 BFU-E/kg (n=35) versus 23 clays (median 20 days) in patients receiving allografts containing < 1.0 x 10 5 BFU-E/kg (n=24). Seven patients receiving allografts containing less than 0.5 x 10 5 BFU-E/kg had primary platelet engraftment failure. The present study has identified the high number of progenitor cells in the allografts infused and the daily administration of G-CSF post-transplant as the optimal combination for a rapid neutrophil recovery after alloBMT. More significantly, the number of BFU-E in allografts was the most significant factor to determine platelet recovery after alloBMT. The development of GVHD of grade II or more during the first weeks after alloBMT was associated with slower haematological recovery and longer period of fever during neutropenia and hospitalisation.
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