High-dose chemotherapy and autologous bone marrow transplantation in acute myeloid leukemia

AK McMillan(Middlesex University), AH Goldstone(Middlesex University), DC Linch(Middlesex University), JG Gribben(Middlesex University), KG Patterson(Middlesex University), J. D. M. Richards(Middlesex University), I Franklin(Middlesex University), BJ Boughton(Middlesex University), DW Milligan(Middlesex University), M. J. Leyland(Middlesex University)
Blood
August 1, 1990
Cited by 83Open Access
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Abstract

For younger patients with acute myeloid leukemia (AML), an allogeneic transplant from a matched sibling may afford the best chance of cure. In patients who are older or without a matched sibling donor, dose intensification can be achieved with an autologous bone marrow transplant (ABMT). We report here the results of a high-dose chemotherapy regime with nonpurged ABMT in 82 adult patients in first remission of AML with a median follow-up of 31 months. The median age was 40 years (range 16 to 57 years). The median interval between remission and ABMT was 5 months (range 1 to 12 months). Twenty-eight of these patients received a second course of the same high-dose chemotherapy and ABMT. The procedure related mortality rate was 6%. The projected leukemia-free survival (LFS) at 5 years is 48% for all 82 patients and 50% for the 76 patients with no known preceding myelodysplastic syndrome. For those patients with primary AML who received a double ABMT the projected LFS is 67%. The interval between remission and ABMT did not predict for either relapse or LFS. ABMT using a multidrug chemotherapy protocol is less toxic than allogeneic BMT yet results in a similar LFS.


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