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Autologous Bone Marrow Transplantation - Blog Science Connections

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ABMTinCRl 45<br />

Induction<br />

V A D<br />

C- V A<br />

D<br />

MTX, L-ASP X 4<br />

Consolidation Adriamycin + HD-ARA-C X 1<br />

CBV + ABMT<br />

maintenance chemotherapy<br />

M-DOMP X 6<br />

Figure 2. Treatment schema for ALL in first complete remission.<br />

after high-dose cytarabine, bone marrow was collected for transplantation. The<br />

median period between onset of remission and transplantation was 6 months<br />

for AML and 7 months for ALL. After transplantation, when hematopoietic<br />

recovery was complete, maintenance chemotherapy was restarted. After<br />

transplantation six courses of AD-OAP were administered for AML and six<br />

courses of MTX-DOMP for ALL.<br />

The study of AML was originally designed as a randomized study between<br />

transplantation and continuation of normal-dose chemotherapy without highdose<br />

intensification. However, the randomization failed because patients<br />

refused to enter the protective environment for the second time (remission<br />

induction occurred in the protective environment) and because of the potential<br />

risk involved in the CBV program. For this reason, patients were selected on a<br />

voluntary basis. The study of ALL was a one-arm study that included treatment<br />

with CBV.<br />

For the first 10 days after transplantation, patients were treated with<br />

acyclovir and with prophylactic antibodies to decontaminate the intestinal tract.

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