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Table 2. Autologous BMT in ALL in first remission<br />

Rowe 59<br />

Reference No. patients Median age (years) Disease-free survival<br />

EBMT, 1995 10 834 30(18-51) 42 ± 4 (8 years)<br />

Fière, 1993 8 63 NS 51 (5 years)<br />

Blaise, 1990 12 22 31 (7^17) 40 (3 years)<br />

Kantarjian, 1990 13<br />

26 30 60 (3 years)<br />

Carey, 1991 14 15 30(18-51) 57 (3 years)<br />

Powles, 1995 15 50 26 (15-58) 53 (3 years)<br />

Vey, 1994 16 34 29(16-59) 27 (8 years)<br />

Attal, 1995 17 64 NS 29 (3 years)<br />

reports (Table 2). The problem is that so little of this is controlled, <strong>and</strong> there has<br />

only been one previous prospective study attempting to define the role of<br />

<strong>autologous</strong> bone <strong>marrow</strong> <strong>transplantation</strong>. 8<br />

Data from the European Transplant<br />

Bone Marrow Group describe a disease-free survival of 42% among "st<strong>and</strong>ard<br />

risk" patients. 78<br />

However, it must be remembered that these are retrospective data<br />

taken from a multitude of centers with patient selection making interpretation<br />

difficult.<br />

The French study reported by Fière in 1993 8<br />

suggested, in a prospective study,<br />

that the response to <strong>autologous</strong> bone <strong>marrow</strong> <strong>transplantation</strong> may be at least as<br />

good as conventional chemotherapy. It is reassuring that the recent update 11<br />

of this<br />

study has not changed very much, with a median follow-up now of more than 8<br />

years (Table 3). In this prospective study, allogeneic <strong>transplantation</strong> remains statistically<br />

superior among patients with "high-risk" ALL emphasizing, with long-term<br />

follow-up, the potential for cure in this group.<br />

Nevertheless, the entire issue of <strong>autologous</strong> bone <strong>marrow</strong> <strong>transplantation</strong><br />

remains uncertain, as is the precise role of allogeneic BMT in first remission for<br />

patients who are not at high risk. A major prospective study is currently underway<br />

with a trans-Atlantic effort between the Eastern Cooperative Oncology Group in<br />

the United States <strong>and</strong> the Medical Research Council in Britain (ECOG 2993 <strong>and</strong><br />

Table 3. Allogeneic <strong>and</strong> <strong>autologous</strong> BMT in first complete remission French Group on<br />

Therapy of Adults ALL—Fiere et al.<br />

Post-CR (intent-to-treat) Allogeneic BMT Autologous BMT Chemotherapy<br />

n 116 95 191<br />

DFS 43% _ 39% 32%<br />

JCO, 1993 8<br />

DFS 46% 34% 30%<br />

ASCO, 1998 11<br />

High risk 44% 16% 11%<br />

St<strong>and</strong>ard risk 49% 49% 39%

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