Abstract
To assess the clinical significance of AML1/ETO gene detected by nested reverse transcriptase polymerase chain reaction, the outcome of 7 patients with acute myeloblastic leukemia between 3 and 14 years of age were presented. All patients had complete remission (CR) at the end of induction (AML-MRC 10 protocol) and 4 underwent unpurged autologous, 2 allogeneic (from matched siblings) non-T-cell-depleted bone marrow transplantations (BMT) in first CR. One patient died due to allogeneic BMT-related complications, and 4 patients relapsed at 13, 17, 18, and 26 months. Only one patient achieved second CR. All relapsed patients died between 18 and 36 months with resistant disease (n = 3) or infection during salvage chemotherapy (n = 1). Two patients who had autologous BMT are alive and disease free at 44 and 50 months. Although statistical significance could not be shown, event-free survival and overall survival rates of AML1/ETO-positive patients (28.57 and 28.57%, respectively) at 3.5 years were even lower than those of AML1/ETO-negative patients. The results confirm some previous reports that AML1/ETO gene in children and adolescents is not a favorable prognostic factor.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adolescent
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Bone Marrow Transplantation
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Child
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Child, Preschool
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Combined Modality Therapy
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Core Binding Factor Alpha 2 Subunit
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Disease-Free Survival
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Female
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Gene Expression
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Humans
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Leukemia, Monocytic, Acute / genetics
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Leukemia, Monocytic, Acute / metabolism
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Leukemia, Monocytic, Acute / therapy
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Leukemia, Myeloid, Acute / genetics*
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Leukemia, Myeloid, Acute / metabolism
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Leukemia, Myeloid, Acute / therapy
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Leukemia, Myelomonocytic, Acute / genetics
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Leukemia, Myelomonocytic, Acute / metabolism
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Leukemia, Myelomonocytic, Acute / therapy
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Leukemia, Promyelocytic, Acute / genetics
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Leukemia, Promyelocytic, Acute / metabolism
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Leukemia, Promyelocytic, Acute / therapy
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Male
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Oncogene Proteins, Fusion / biosynthesis
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Oncogene Proteins, Fusion / genetics*
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RNA, Messenger / analysis
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RNA, Messenger / genetics
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RUNX1 Translocation Partner 1 Protein
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Remission Induction
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Reverse Transcriptase Polymerase Chain Reaction
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Transcription Factors / biosynthesis
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Transcription Factors / genetics*
Substances
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AML1-ETO fusion protein, human
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Core Binding Factor Alpha 2 Subunit
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Oncogene Proteins, Fusion
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RNA, Messenger
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RUNX1 Translocation Partner 1 Protein
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Transcription Factors