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Autologous Bone Marrow Transplantation - Blog Science Connections

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ABMTfor Neuroblastoma 381<br />

PATIENTS<br />

B3<br />

BB7<br />

12<br />

• BEFORE PURGING<br />

J MARRON SEDIMENTED<br />

3 TO ENRICH FOR TUMOR<br />

AFTER SEDIMENTATION<br />

AND FILTRATION<br />

I AFTER MAGNETIC<br />

IIMMUNOBEAOS<br />

BB6<br />

]8<br />

BB15<br />

0 1<br />

0<br />

5.5<br />

10 15 20<br />

TUMOR CELLS/100. 000 MARROW CELLS<br />

Figure 3. Removal of neuroblastoma cells from autologous marrow by sequential<br />

sedimentation, filtration, and magnetic immunobead treatment. <strong>Marrow</strong> from four<br />

patients (B3, BB7, BB6, and BB15) was treated with one cycle of immunobeads coated<br />

with goat antimouse immunoglobulin and monoclonal antibodies 390,459, HSAN 1.2, and<br />

BA-1. Tumor cells were identified in marrow by immunoperoxidase staining with<br />

anti-cell-surface monoclonal antibodies (mixture of antibodies 390, 459, HSAN 1.2, and<br />

126-4) and with anti-neuron-specific enolase serum.<br />

diagnosed patients into the BMT phase by 20 weeks after diagnosis without<br />

progressive disease and to emerge from the BMT phase with a 90% survival rate.<br />

Because all patients are not expected to remain tumor-free following BMT,<br />

efforts are being made to identify prognostic factors for this very aggressive<br />

therapeutic approach; additional or different therapy will need to be developed<br />

for those who are likely to develop progressive disease after BMT. Collectively,<br />

these new strategies may further increase the percentage of patients who<br />

survive tumor free.<br />

ACKNOWLEDGMENTS<br />

This study was supported in part by U.S. Public Health Service grants<br />

CA12800, CA27678, and CA16042 from the National Cancer Institute, U.S.<br />

Department of Health and Human Services; by a grant from Concern II; and by

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