VI Autologous Bone Marrow Transplantation.pdf - Blog Science ...
VI Autologous Bone Marrow Transplantation.pdf - Blog Science ...
VI Autologous Bone Marrow Transplantation.pdf - Blog Science ...
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COMPARISON OF INTENSIVE CONSOLIDATION CHEMOTHERAPY<br />
(ICC) AND UNPURGED AUTOLOGOUS BONE MARROW<br />
TRANSPLANTATION (ABMT) AS POST REMISSION THERAPY IN<br />
ADULT ACUTE MYELOID LEUKEMIA (AML).<br />
JL Harousseau*, JY Cahn, B Pignon, D Mignard, F Witz, C Linassier, N Ifrah,<br />
B Lioure, D Caillot, F Guilhot, JF Abgrall, PY Leprise, D Guyotat, P Casassus,<br />
J Briere, F Mors, B Desablens, P Hurteloup on behalf of the GOELAM group.<br />
* Department of hematology - C.H.U. NANTES - FRANCE<br />
INTRODUCTION<br />
Recently published series have shown that a disease free survival of 30 to<br />
50% could be achieved after short term Intensive Consolidation Chemotherapy<br />
(ICC) without maintenance treatment 15<br />
. <strong>Autologous</strong> <strong>Bone</strong> <strong>Marrow</strong> <strong>Transplantation</strong><br />
(ABMT) after myeloablative treatment is another attractive approach. In pilot<br />
single center studies or in the annual survey of the European registry, disease<br />
free survival rates around 50% were obtained However in all these studies,<br />
the issue of patient selection was raised. Thus, randomized studies comparing<br />
ABMT and ICC were mandatory. In 1987, the French group GOELAM initiated<br />
such a study.<br />
PATIENTS AND METHODS<br />
Patients (pts) aged 15 to 50 years with de novo AML were included in a<br />
multicenter study involving 16 centers of the GOELAM group. Pts with preexisting<br />
myelodysplastic syndromes or with blastic transformation of chronic<br />
myeloproliferative disorders were not included. Chemotherapy/radiation-induced<br />
leukemias were also excluded. From November, 1987 to December 1991,<br />
318 pts were enrolled and 308 pts are évaluable.<br />
INDUCTION TREATMENT<br />
Patients were randomized to induction treatment between Cytarabine (Ara-<br />
C) 200 mg/m 2<br />
/d (continuous infusion) for 7 days plus Idarubicin (IDR) 8 mg/<br />
m 2<br />
/d IV for 5 days and ARA-C at the same dosage plus Zorubicine (ZRB) 200<br />
mg/m 2<br />
for 4 days. A bone marrow aspiration was performed at day 17: if the<br />
marrow remained blastic (< 50% blasts) a second course was administered with<br />
3 days of Ara-C plus 2 days of either IDR 10 mg/m 2<br />
/d or ZRB 200 m g /m 2<br />
/d .<br />
POST REMISSION TREATMENT<br />
Pts in complete remission (CR) were allografted if they were under the age<br />
of 40 years and had an HLA-identical sibling. The conditioning regimen and the<br />
graft versus host disease prophylaxis and treatment varied according to protocols<br />
used in the different transplant centers. Pts over 40 years or without a suitable<br />
donor received a first course of ICC (ICC1 ) Ara-C (3 g/m 2<br />
in 3 hours infusion<br />
every 12 hours for eight doses, dl to d4) and either IDR 10 mg/m 2<br />
/d d5-6<br />
16 SIXTH INTERNATIONAL SYMPOSIUM ON AUTOLOGOUS BONE MARROW TRANSPLANTATION