2007
DOI: 10.1016/j.bbmt.2006.12.021
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18: Autologous peripheral blood stem cell transplant using busulfan, etoposide, high dose Ara-C, and G-CSF priming as conditioning regimen in patients with acute myeloid leukemia in first complete remission

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“…However, we should highlight a considerably lower NRM in patients who received BEA (0.6% at 2 years and 1.5% at 5 years), con rming previous results with this conditioning regimen. 5,7,8 Replacement of the alkylating agents cyclophosphamide and melphalan with more speci c AML drugs, such as the topoisomerase inhibitor etoposide and the DNA polymerase inhibitor cytarabine, could have led to reduced toxicity.…”
Section: Discussionmentioning
confidence: 99%
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“…However, we should highlight a considerably lower NRM in patients who received BEA (0.6% at 2 years and 1.5% at 5 years), con rming previous results with this conditioning regimen. 5,7,8 Replacement of the alkylating agents cyclophosphamide and melphalan with more speci c AML drugs, such as the topoisomerase inhibitor etoposide and the DNA polymerase inhibitor cytarabine, could have led to reduced toxicity.…”
Section: Discussionmentioning
confidence: 99%
“…Following encouraging preliminary results, 5,6 another alternative to the classic BUCY regimen, replacing cyclophosphamide with etoposide and high-dose cytarabine (BEA regimen), along with granulocyte colony-stimulating factor (G-CSF) priming, has been increasingly used in patients with AML in CR1. [7][8][9] The promising results reported with BEA prompted us to compare the safety and e cacy of BEA, BUMEL, and BUCY as preparative regimens for ASCT in patients with AML in CR1, registered in the EBMT database.…”
Section: Introductionmentioning
confidence: 99%