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66 Chapter 2: ALL<br />

recent update, however, demonstrated an advantage in terms of LFS for alloBMT<br />

compared with chemotherapy in patients 30 years old, results of chemotherapy <strong>and</strong> BMT were similar (30 vs.<br />

26%). 16<br />

It seems that with better management of BMT complications <strong>and</strong> a<br />

reduction in TRM, the BMT indications in adult ALL in CR1 may be extended.<br />

Several groups also failed to demonstrate a statistically significant advantage<br />

for alio- or autoBMT in first CR compared with chemotherapy in prospective<br />

trials. 6,1517<br />

" 19<br />

The French study group conducted a r<strong>and</strong>omized trial with autoBMT<br />

vs. chemotherapy in patients without a sibling donor <strong>and</strong> alloBMT for all patients<br />

with sibling donors. LFS in patients treated with alloBMT (44%) was not significantly<br />

superior to those treated with chemotherapy (32%). In high-risk patients,<br />

however, there was a significantly better LFS for patients treated with alloBMT<br />

(39%) compared with those in the control group (14%) treated with either<br />

chemotherapy or autoBMT (Table 2). 20<br />

It remains an open question whether autoBMT or chemotherapy is superior in<br />

adult ALL patients in CR1. Generally there was a trend in favor of autoBMT<br />

compared with chemotherapy which did not reach statistical significance. Thus,<br />

two groups reported a higher LFS after <strong>autologous</strong> BMT compared with<br />

chemotherapy, 54 vs. 35% 21<br />

<strong>and</strong> 48 vs. 20-30% (depending on chemotherapy<br />

protocol), respectively. 19<br />

Both trials, however, included small patient numbers of<br />

26 vs. 19 patients 21<br />

<strong>and</strong> 19 vs. 72 patients. 19<br />

In the large prospective, r<strong>and</strong>omized<br />

French trial, autoBMT was not superior to chemotherapy with similar TRM (4 vs.<br />

4%), RI (57 vs. 61 %), <strong>and</strong> LFS (39 vs. 32%). 6<br />

IDENTIFICATION OF HIGH-RISK PATIENTS<br />

ALL is not a uniform disease but can be separated into subgroups with considerably<br />

different LFS ranging between 50%. In addition to the<br />

"st<strong>and</strong>ard" clinical risk factors (white <strong>blood</strong> cell [WBC] count, age, time to CR) 22<br />

Table 2. Comparison of alloBMT <strong>and</strong> chemotherapy as postremission therapy in adult<br />

ALL<br />

DSF TRM RI<br />

Group AlloBMT Chemo AlloBMT Chemo AlloBMT Chemo<br />

Fiereetal. 1993 6<br />

Zhang et al. 1995 414<br />

Mrsic et al. 1993 19<br />

Oh et al. 1995 16<br />

Formanet al. 1995 18<br />

NR, not reported; RI, relapse incidence.<br />

44% (116) 32% (96) 16%+ 4%+ 41% 61%<br />

34% (234) 32% (484) 53% 5% 30% 66%<br />

52% (22) 20-30% (43) NR NR 20% 70-80%<br />

33% (250) 27% (80) 54% 12% 28% 69%<br />

66% (37) 55% (66) NR NR 9% 38%

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