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32 Chapter 1:AML<br />

Table 3. Probability of 1-, 2-, <strong>and</strong> 3-year survival by regimen <strong>and</strong> remission status<br />

Overall survival Disease-free survival<br />

Factor n / year 2 years 3 years 1 year 2 years 3 year<br />

Remission status<br />

CR1 23 0.54 0.50 0.50 0.50 0.50 0.50<br />

CR2/3 87 0.46 0.36 0.33 0.40 0.32 0.27<br />

Rl 28 0.56 0.40 0.35 0.33 0.33 0.33<br />

Conditioning regimen<br />

Cy/TBI 35 0.46 0.37 0.34 0.37 0.34 0.31<br />

BU/Cy 93 0.53 0.42 0.39 0.44 0.37 0.34<br />

BU/VP16 10 0.30 0.20 — 0.20 0.20<br />

Conditioning regimen/status<br />

CR1<br />

Cy/TBI 7 0.87 0.71 0.71 0.71 0.71 0.71<br />

BU/Cy 12 0.45 0.45 0.45 0.45 0.45 0.45<br />

BU/VP16 4 0.25 0.25 0.25 0.25 0.25 —<br />

CR2/3<br />

Rl<br />

Cy/TBI 26 0.35 0.31 0.27 0.31 0.27 0.23<br />

BU/Cy 55 0.54 0.49 0.38 0.47 0.36 0.31<br />

BU/VP16 6 0.33 0.17 — 0.17 0.17 —<br />

Cy/TBI 2 0.5 — — 0 — —<br />

BUCy 26 0.56 0.43 0.38 0.37 0.37 0.37<br />

mAb-based techniques using antimyeloid mAbs have been used to purge AML<br />

<strong>marrow</strong>. This report updates our > 10-year multi-institutional clinical data of<br />

autoBMT in AML with mAb <strong>and</strong> C'-mediated purging. As with allogeneic BMT,<br />

the results are dependent on remission status. Five-year DFS for patients<br />

transplanted in Rl <strong>and</strong> CR2/3 who were conditioned with Bu/Cy2 were 37 <strong>and</strong><br />

28%, respectively. These results compare favorably with those of allogeneic<br />

4 3 1<br />

BMT.<br />

Significant prognostic factors operating in our study were length of first CR (for<br />

patients transplanted in Rl or CR2/3) <strong>and</strong> sex. Interestingly, patients with<br />

secondary AML or extramedullary disease did not fare worse. Nor did cytogenetics<br />

of AML cells at diagnosis affect outcome (although some of the patient subgroups<br />

were small). These results are surprising, since prior central nervous system (CNS)<br />

disease <strong>and</strong> cytogenetic abnormalities have been associated with worse outcomes<br />

in previous studies. 32-34<br />

We have conducted a phase II clinical trial of monoclonal antibody purging of<br />

bone <strong>marrow</strong> in patients with AML in remission at the time of harvest <strong>and</strong> in<br />

remission or relapse at the time of transplant. The overriding question raised by the

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