N. Vey et al., BONE-MARROW TRANSPLANTATION IN 63 ADULT PATIENTS WITH ACUTE LYMPHOBLASTIC-LEUKEMIA IN FIRST COMPLETE REMISSION, Bone marrow transplantation, 14(3), 1994, pp. 383-388
Over a 10 year period, we transplanted 63 patients with acute lymphobl
astic leukaemia (ALL) who had achieved first complete remission (CR).
All were > 15 years old and 45 (71%) had at least one poor prognostic
factor. Twenty-nine patients with a suitable sibling underwent autolog
ous bone marrow transplantation (BMT). Beginning in 1984, patients wit
hout a donor received an allogeneic BMT (34 patients). Preparation con
sisted of cyclophosphamide (CY)/TBI (78%) or melphalan (Mel)/TBI (22%)
; marrow was treated in vitro in 31 patients (allogeneic: 7; autologou
s: 24). Kaplan-Meier estimates of the probability at 6 years of relaps
e, survival and DFS were 41% (allogeneic: 10%, autologous: 65%, p < 0.
05), 44% (allogeneic: 62%, autologous: 26%, p = NS) and 42% (allogenei
c: 62%, autologous: 27%, p < 0.06), respectively. This report confirms
that allogeneic BMT permits long-term remissions giving high levels o
f survival when performed shortly after entering first CR while autolo
gous BMT, when performed in the same setting, is less successful at pr
eventing relapse. This study also confirms the high sensitivity of ALL
to the graft-versus-leukemia effect provided by allogeneic BMT. Chemo
radiotherapy dose intensification delivered at autologous BMT is not s
ufficient to prevent relapses. Autologous BMT must therefore be augmen
ted by other approaches of which immunotherapy may be one.