Secondary
myelodysplastic syndrome (MDS) and acute
leukemia (AL) are well-known complications of
antineoplastic therapy. The incidence of these serious complications after autologous hematopoietic
transplantation ranges from 1.1% to 24%. Prior
chemotherapy is its most likely cause, but other variables related to these long-term complications are seriously discussed. There is evidence that priming of progenitor cells isolated from peripheral blood with
chemotherapy is also related to a higher risk of secondary MDS/AL. Whether progenitor cells isolated from bone marrow or peripheral blood after mobilization only with
cytokines are related to higher risk is a controversial issue. In this paper, we analyze the incidence and variables related to these complications in a series of 99 patients diagnosed with
lymphoma or
multiple myeloma who underwent
autologous transplantation using hematopoietic progenitors isolated from peripheral blood mobilized with
granulocyte colony-stimulating factor (
G-CSF). The probability of MDS/AL in patients alive 5 years after transplant in our series is 8.58%, similar to that reported in other series using bone marrow grafts. The total dose of
cyclophosphamide ( p=0.099), the number of
chemotherapy cycles ( p=0.04) received before transplant, and the total dose of mononuclear cells infused at the time of transplant were the only variables associated with secondary MDS/AL.
Autologous transplantation with progenitor cells isolated from peripheral blood after mobilization with
cytokines has probability and risk factors for secondary MDS/AL development similar to bone marrow grafts when compared with other published series.