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Autologous Bone Marrow Transplantation - Blog Science Connections

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ABMT In CR2 57<br />

CR INVERSION: 2/22 - 9!<br />

MONTHS<br />

12<br />

Figure 2. Updated results of CBV (cyclophosphamide, BCNU [carmustine], and etoposide)<br />

plus unpurged ABMT in second and subsequent remissions. Complete remission<br />

inversion indicates subsequent remissions longer than the preceding ones.<br />

12 months or longer. In two, the transplantation remission was longer than<br />

the preceding remission, producing an inversion rate of 9%. Because the 95%<br />

confidence limit extends from 0 to 21 %, we consider a study positive when the<br />

inversion rate is at least 22%. According to these criteria, Yeager's and<br />

Ramsay's studies are promising.<br />

In our opinion, better results can be obtained when the two methods of<br />

purging—the chemoseparation technique and a monoclonal antibody-based<br />

technique—are combined. This combination of methods reduces the<br />

influence of drug resistance and of antigenic heterogeneity. Therefore, we<br />

have initiated a transplantation program for second and subsequent<br />

remissions in which we can ultimately combine the two technologies.<br />

Before we can do this, phase 1 studies of both chemopurging alone and of<br />

the magnetic affinity colloid (MAC) technique need to be carried out<br />

separately to determine the influence of both on hematopoietic recovery. In<br />

chemopurging, the marrow cells are incubated with 4-HC plus vincristine,<br />

inhibitory concentrations 75 and 90. The MAC technique is different for AML<br />

and non-T-cell ALL. For AML, it employs SBA, CF1, PM81, and MY7

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