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Autologous Bone Marrow Transplantation - Blog Science Connections

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688 Peripheral Blood Stem Cell <strong>Transplantation</strong><br />

facilitate bone marrow stem cell collections when feasible. In some cases,<br />

however, extensive marrow contamination by tumor or prior radiotherapy limits<br />

the availability of bone marrow stem cells. Also, in rare cases general or regional<br />

anesthesia necessary for bone marrow stem cell harvesting is associated with<br />

an unacceptable risk to the patient. Peripheral blood stem cells (PBSCs)<br />

obtained by multiple leukapheresis circumvents the problem of availability and<br />

may be associated with less frequent tumor cell contamination. The following<br />

case and review are presented to illustrate several points regarding this<br />

treatment.<br />

MATERIALS AND METHODS<br />

Using the IBM 2997 cell separator we collected stem cells eight separate<br />

times from a patient with relapsed Hodgkin's disease. The initial two procedures<br />

took 3 hours each, and the remaining six took a full 4 hours each. Most of the<br />

procedures were performed using a Vascath central venous catheter (Gambro,<br />

Lincolnshire, 1L) as access for both the draw and return lines. Flow rates and<br />

centrifuge speeds were selected for optimum peripheral blood mononuclear<br />

cell (PBMC) collection. These were a flow rate of 40 ml/minute with a centrifuge<br />

speed of 938 rpm or a flow rate of 45 ml/minute with a centrifuge speed of 995<br />

rpm. Collected volumes varied from 198 ml to 300 ml. The resulting cell<br />

suspensions were adjusted to 10 U/ml with heparin before further processing.<br />

The buffy coat was isolated from the cell suspensions and cryopreserved at<br />

a concentration of 10 8 /ml using 10% dimethyl sulfoxide and 20% autologous<br />

plasma from which cryoprecipitate was previously removed for freezing<br />

medium as described elsewhere (2). Samples from each separate batch were<br />

analyzed for granulocyte-macrophage colony-forming units (CFUs-GM) and<br />

erythroid burst-forming units (BFUs-E) immediately and after thawing.<br />

RESULTS<br />

The patient, a 20-year-old man, initially presented with Hodgkin's disease,<br />

stage IIIB. After initial complete remission after therapy with mechlorethamine,<br />

Oncovin (vincristine), procarbazine, and prednisone combined with Adriamycin<br />

(doxorubicin), bleomycin, vinblastine, and dacarbazine (MOPP-ABVD), he<br />

relapsed on two subsequent occasions. His subsequent treatment involved<br />

MOPP-ABVD, mantle radiation to 37 Gy, CCNU (lomustine), methotrexate,<br />

etoposide, another series of MOPP-ABVD, and most recently cytarabine,<br />

cisplatin, and dexamethasone.<br />

In May 1986 high-dose chemotherapy with autologous bone marrow<br />

transplantation was planned. Results of bilateral bone marrow biopsies were<br />

negative for involvement with Hodgkin's disease, so multiple bone marrow<br />

aspirations were performed with the patient under general anesthesia. Cells<br />

were cryopreserved. In the course of this process, six separate iliac crest bone

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