Abstract

Braz J Med Biol Res, January 1998, Volume 31(1) 49-53

New strategies in hematopoietic stem cell transplantation: G-CSF-mobilized unprocessed whole blood

A.M. Dräger, G.J. Ossenkoppele, A.R. Jonkhoff, G.J. Schuurhuis and P.C. Huijgens

Department of Hematology, Free University Hospital, Amsterdam, The Netherlands

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References

Correspondence and Footnotes ^{Correspondence and Footnotes} Correspondence and Footnotes

Transplantation of mobilized peripheral blood stem cells (PBSC) for rescue of bone marrow function after high-dose chemo-/radiotherapy is widely used in hematologic malignancies and solid tumors. Mobilization of stem cells to the peripheral blood can be achieved by cytokine treatment of the patients. The main advantage of autologous PBSC transplantation over bone marrow transplantation is the faster recovery of neutrophil and platelet counts. The threshold number of PBSC required for adequate rescue of bone marrow is thought to be about 2 x 10⁶ CD34⁺ cells/kg, if the stem cells are collected by leukapheresis and subsequently cryopreserved. We show that this critical number could be further reduced to as few as 0.2 x 10⁶ cells/kg. In 30 patients with multiple myeloma and 25 patients with bad risk lymphoma 1 liter of granulocyte colony-stimulating factor (G-CSF)-mobilized unprocessed whole blood (stored at 4^oC for 1-3 days) was used for transplantation. Compared to a historical control group, a significant reduction in the duration of neutropenia, thrombocytopenia and the length of hospital stay was documented. Furthermore, the effect of stem cell support was reflected by a lower need for platelet and red cell transfusions and a reduced antibiotic use. Considering the data as a whole, a cost saving of about 50% was achieved. To date, this easy to perform method of transplantation is only feasible following high-dose therapies that are completed within 72 h, since longer storage of unprocessed blood is accompanied by a substantial loss of progenitor cell function. Ongoing investigations include attempts to prolong storage times for whole blood.

Abstract

Key words: hematopoietic stem cells, transplantation, cytokines, G-CSF, lymphoma, multiple myeloma

Mobilization of hematopoietic stem cells

Dührsen et al. (1) were the first to demonstrate that administration of recombinant granulocyte colony-stimulating factor (G-CSF) increases the number of colony-forming units in peripheral blood up to 100-fold steady-state levels. In normal individuals the number of mobilized peripheral blood stem cells (PBSC) depends on the dose of G-CSF used (5-15 µg/kg, sc, 4-6 days, daily (2) or twice daily (3)) and the age of the donor, whereas the stem cell yield in patients who have been previously subjected to therapy strongly depends on the number of courses of chemotherapy or radiotherapy (4-6). Recently, the advantages of G-CSF-mobilized peripheral blood progenitor transplantation vs autologous bone marrow transplantation were demonstrated in a randomized trial in patients with lymphoma treated with high-dose chemotherapy (7). The number of platelet transfusions, the time to neutrophil recovery and the period of hospital stay were significantly reduced.

To date, other agents with the potential to mobilize stem cells but which have not yet been tested in clinical trials include GM-CSF, stem cell factor (8,9), IL-8 (10), IL-3, IL-6, IL-11 (11), and antibodies directed against the adhesion molecule VLA-4 (CD49d). Apart from cytokines, the number of circulating PBSC can be increased by chemotherapy during hematopoietic recovery as originally observed by Richman et al. (12). However, the stem cells harvested contain a smaller portion of primitive progenitor cells compared to G-CSF alone, as measured by the the lack of HLA-DR or CD38 in the CD34⁺ cell population. In addition, a combination of cytokine administration following chemotherapy has been reported to effectively mobilize stem cells (reviewed in Ref. 13).

Patients in whom stem cells are poorly mobilized have to undergo several cycles of leukapheresis to collect enough stem cells for long-term repopulation of the bone marrow. The threshold number of PBSC required for adequate rescue of bone marrow is about 2 x 10⁶ CD34⁺ cells/kg (reviewed in Ref. 13), if the stem cells are collected and cryopreserved. During cryopreservation loss of quality of the transplant may occur, since we could show that the critical number of stem cells for rescue could further be reduced to as few as 0.2 x 10⁶ cells/kg if 1 liter of mobilized unprocessed whole blood was reinfused (14-16).

Clinical studies involving G-CSF-mobilized unprocessed whole blood

Studies by Molineux et al. (17) showed that the amount of blood required to rescue lethally irradiated mice could be reduced from 3 ml (1.5 times the normal blood volume) to 10 µl when using blood of mice which were pretreated with G-CSF. Furthermore, it was shown that blood of G-CSF-treated mice contained hematopoietic stem cells functionally comparable to bone marrow-derived stem cells (18). The authors presumed that about 5 ml of stimulated unprocessed blood/kg body weight may be sufficient for successful engraftment in humans. We tested the feasibility of unprocessed blood treatment first in a small group of patients (N = 5) with multiple myeloma receiving high-dose melphalan (HDM; 140 mg/m2) at day 0 (14). To date, the study has been extended to more than 30 patients (16). In this study, 10 µg/kg G-CSF (filgrastim; Neupogen Amgen, Thousand Oaks, CA, USA) was administered sc daily starting on day -6 for 6 days. On day 0, two phlebotomies of 500 ml each were performed via an antecubital vein and melphalan was given intravenously. After 24 h the two bags of blood were reinfused. The median number of CD34⁺ cells in blood after mobilization was 0.3 x 10⁶/kg (range 0.1-1.75). Compared with a historical control group of 20 patients treated with HDM without stem cell rescue, the median duration of neutropenia was reduced by 24 days, the median duration of thrombocytopenia by 10 days and the median length of hospital stay by 24 days. The effect of stem cell support was also reflected by a lower need for platelet and red cell transfusions and a reduced antibiotic use. Besides reduced toxicity, a cost saving of about 50% was calculated (19).

In another study (15) the whole blood stem cell procedure was adapted to a modified (72-h course) myeloablative BEAM-like scheme in 9 patients with bad risk malignant lymphomas. In this treatment protocol the blood was stored unprocessed for 3 days at 4^oC before reinfusion. The scheme was adjusted in such a way that the cytostatics used had been largely cleared from the blood by the day of reinfusion. The median number of reinfused CD34⁺ stem cells was 0.28 x 10⁶/kg (range 0.01-0.59). When more than 0.2 x 10⁶/kg CD34⁺ cells were reinfused the time to recovery was comparable to that observed after classical peripheral stem cell transplantation (15).

Liquid storage of peripheral blood progenitors

To date we only employ this attractive method of autologous stem cell transplantation using 1 liter of unprocessed whole blood if high-dose chemotherapy is completed within 72 h since longer storage of unprocessed blood is accompanied by a substantial loss of progenitor cells. We could show that the number of CD34⁺ cells in blood from G-CSF-treated patients with lymphoma even increased in 12/20 patients after 3 days of storage at 4^oC as compared to day 0. Storage at 24^oC resulted in a reduced number of progenitor cells after 3 days. Studies on the feasibility of storage for longer periods of time were hampered by the fact that only small amounts of blood were still available after reinfusion of the bulk on day 3. Comparing the quality of progenitor cells during the first 3 days, we found better results when the blood was stored in a larger volume compared to a smaller volume. Improvement of the storage conditions is necessary to extend the whole blood procedure to other chemotherapeutic regimens. The addition of G-CSF at a concentration of 10 ng/ml to cells in storage showed no detectable benefit (20). In this study, 77% of the initial colony-forming units remained after 96 h at 4^oC. Our findings are also in accordance with the study of Pettengell et al. (21) who established that hematopoietic progenitors in leukapheresis material and in whole blood remain viable for 5 days at 4^oC. The use of non-cryopreserved mobilized blood stem cells has also been described by others (22,23). In these studies, however, leukapheresis material was used.

Role of adhesion molecules in the mobilization of stem cells and their homing to bone marrow

Although the underlying mechanisms of mobilization are largely unknown, it is evident that adhesion molecules play a crucial role in this process. Mobilization may be the result of downregulation of adhesion molecules on stem cells which would enable these cells to be recruited with increased efficacy into the peripheral blood. Candidate adhesion molecules are LFA-1, VLA-4, VLA-5 and LFA-3 since these molecules are expressed in lesser amounts on PBSC as compared to their bone marrow counterparts (24-26).

On the other hand, the expression of these cell surface markers on stem cells can be expected to be important for effective engraftment after reinfusion. Important structures involved in the `homing' of PBSC to the bone marrow include the selectin family of adhesion molecules and their glycoprotein ligands. Blood-derived stem cells express high levels of CD62L (L-selectin) as compared to bone marrow stem cells (24). This observation may explain the improved kinetics of bone marrow recovery after PBSC transplantations, since it has been described that the number of reinfused CD34⁺/CD62L⁺ stem cells correlates better with the time needed for platelet recovery than the total number of CD34⁺ cells (25). On the other hand, it has been shown that neutrophils stimulated with G-CSF upregulate CD11b/CD18 but partly shed their L-selectin receptor (27). Furthermore, G-CSF directly stimulates neutrophil migration across the vascular endothelium (28). It has to be further evaluated whether all of these observations hold true not only for neutrophils but also for stem cells. These observations would be consistent with the role of G-CSF in the mobilization of cells from marrow stores.

Address for correspondence: A. Dräger, Department of Hematology, Free University Hospital, Brug 248, De Boelelaan 1117, NL-1081 HV Amsterdam, The Netherlands. Fax: +31-20-4442601. E-mail: hematol@azvu.nl

Presented at the International Meeting on Cytokines, Angra dos Reis, RJ, Brasil, November 24-28, 1996. Research supported by AMGEN, Holland. Received September 4, 1997. Accepted September 22, 1997.

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