Summary:Reduced post-transplant performance status because of infectious complications is still a problem following autologous peripheral blood stem cell transplantation (aPBSCT). In this study, a tandem transplantation scheme for 15 patients with breast cancer including etoposide (1500 mg/m 2 ), ifosfamide (12 g/m 2 ) and carboplatin (1500 mg/m 2 ) as conditioning regimens, followed by aPBSCT, was used to evaluate the potential clinical benefit of the additional retransfusion of low numbers of ex vivo expanded committed myeloid postprogenitor cells (PPCs) (median 408 Â 103 CFU-c/kg BW, range 0. following the second transplantation. Following a 7+2 days expansion (using recombinant human SCF, IL1b, IL-3, IL-6 + G-CSF), CFU-c generated from CD34-positive cells from leukapheresis products could be expanded by a median factor of 153 (range 5-434). Flow cytometric analysis and morphology of CFUs have shown a nearly exclusive expansion and differentiation of committed myeloid progenitor cells and a significant reduction of CD34-positive cells. In an intra-and interindividual comparison it could be shown that the retransfusion of committed myeloid postprogenitor cells significantly accelerates myeloid recovery. Although retransfusion of PPCs fails to abrogate severe neutropenia following aPBSCT, it significantly ameliorates infectious complications and shortens the duration of hospital stay. The neutropenic period after high-dose chemotherapy (HD-CT) and autologous transplantation may be associated with a high rate of fever and systemic infections. 1,2 The rate of infectious complications increases with the duration of neutropenia. 3 There are several possibilities to shorten the pancytopenic period after autologous transplantation. The use of mobilized peripheral blood stem cells (PBSC) instead of bone marrow (BM) stem cells or increasing the dose of transplanted CD34+ cell dose accelerates the post transplant hemopoietic recovery and improves patients performance after autologous transplantation. 3 However, enhancing the number of CD34+ cells in the transplant over a threshold of 5 Â 10 6 /kg body weight (BW) leads to no further acceleration of neutrophil recovery. 4,5 The additional application of hemopoietic growth factors or growth factor combinations during the post-transplant period has only limited effect on the duration of neutropenia and did not abrogate neutropenic fever in randomized trials. 6 One possible way to overcome the consequences of prolonged neutropenia could be the ex vivo expansion and myeloid differentiation of hematopoietic stem and progenitor cells. Up to now most study groups focused mainly on the expansion of primitive hematopoietic progenitor cells with long-term repopulating ability to abrogate neutropenic fever. 7,8 Furthermore, all studies to date have compared the time to neutrophil recovery with historical controls.In the present study, we have sought to determine if ex vivo expanded postprogenitor cells (PPCs) shorten the neutropenic period, and improve the clinical outcome of pati...