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Comparison of allogeneic stem cell transplantation, high-dose cytarabine, and autologous peripheral stem cell transplantation as postremission treatment in patients with de novo acute myelogenous leukemia

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dc.contributor.author Tsimberidou, AM en
dc.contributor.author Stavroyianni, N en
dc.contributor.author Viniou, N en
dc.contributor.author Papaioannou, M en
dc.contributor.author Tiniakou, M en
dc.contributor.author Marinakis, T en
dc.contributor.author Skandali, A en
dc.contributor.author Sakellari, L en
dc.contributor.author Yataganas, X en
dc.date.accessioned 2014-03-01T01:53:06Z
dc.date.available 2014-03-01T01:53:06Z
dc.date.issued 2003 en
dc.identifier.issn 0008-543X en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/26851
dc.subject de novo acute myelogenous leukemia (AML) en
dc.subject postremission therapy en
dc.subject allogeneic stem cell transplantation en
dc.subject autologous stem cell transplantation en
dc.subject high-dose chemotherapy en
dc.subject.classification Oncology en
dc.subject.other ACUTE MYELOID-LEUKEMIA en
dc.subject.other BONE-MARROW TRANSPLANTATION en
dc.subject.other ACUTE NONLYMPHOCYTIC LEUKEMIA en
dc.subject.other INTENSIVE CONSOLIDATION CHEMOTHERAPY en
dc.subject.other ACUTE MYELOCYTIC-LEUKEMIA en
dc.subject.other FIRST COMPLETE REMISSION en
dc.subject.other CANCER STUDY-GROUP en
dc.subject.other MRC AML-10 TRIAL en
dc.subject.other PHASE-III TRIAL en
dc.subject.other MAINTENANCE CHEMOTHERAPY en
dc.title Comparison of allogeneic stem cell transplantation, high-dose cytarabine, and autologous peripheral stem cell transplantation as postremission treatment in patients with de novo acute myelogenous leukemia en
heal.type journalArticle en
heal.language English en
heal.publicationDate 2003 en
heal.abstract BACKGROUND. Postremission therapy is critical in maintaining complete remission (CR) in patients with de novo acute myelogenous leukemia (AML). The aim of this trial was to compare allogeneic stem cell transplantation (SCT), high-dose cytarabine (ara-C; HiDAC), and autologous SCT as postremission therapy in patients with de novo AML. METHODS. One hundred twenty patients age less than or equal to 60 years with previously untreated AML (non-M3) and a performance status score of less than or equal to 2 received induction therapy with 3 days of idambicin and 7 days of ara-C (IA). Patients in CR received one course of HiDAC. Subsequently, patients age ! 50 years with available HLA-compatible donors were assigned to receive allogeneic SCT; patients with "favorable" cytogenetics received a second course of HiDAC; and all others were randomized to a second course of HiDAC or autologous SCT. RESULTS. The IA combination induced CR in 99 patients (82.5%). With a median follow-up of 43 months (range, 18-64 years), the 3-year survival and failure-free survival (FFS) rates were 47% and 45%, respectively. The factors associated with longer survival were those identified for CR (i.e., age and cvtogenetics). Forty-nine patients (49%) received the assigned postremission therapy. Fifteen patients underwent allogeneic SCT. Nineteen patients underwent autologous SCT and 15 patients received a second course of HiDAC, after randomization. In the allogeneic SCT group, both the 3-year survival and the FFS rates were 73%. In the autologous SCT and HiDAC groups, the 3-year survival rates were 58% and 46%, respectively (P = 0.80), and the 3-year FFS rates were 42% and 33%, respectively (P = 0.83). CONCLUSIONS. The three postremission treatment groups had comparable survival. Allogeneic SCT is associated with a prolonged FFS. en
heal.publisher JOHN WILEY & SONS INC en
heal.journalName CANCER en
dc.identifier.isi ISI:000181816600016 en
dc.identifier.volume 97 en
dc.identifier.issue 7 en
dc.identifier.spage 1721 en
dc.identifier.epage 1731 en


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