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Prospective Analysis of TEL/AML1-positive Patients Treated on Dana-Farber Cancer Institute Consortium Protocol 95-01

Overview
Journal Blood
Publisher Elsevier
Specialty Hematology
Date 2006 Feb 24
PMID 16493009
Citations 33
Authors
Affiliations
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Abstract

In a retrospective analysis, we previously reported that children whose leukemia cells harbored the TEL/AML1 gene rearrangement have excellent outcomes. From 1996 to 2000, we conducted a prospective study to determine the incidence and outcomes of children with TEL/AML1-positive acute lymphoblastic leukemia (ALL). Children with newly diagnosed ALL were treated on DFCI ALL Consortium Protocol 95-01. Patients were risk stratified primarily by current National Cancer Institute (NCI)-Rome risk criteria. With a median follow-up of 5.2 years, the 5-year event-free survival for TEL/AML1-positive patients was 89% compared with 80% for TEL/AML1-negative B-precursor patients (P = .05). The 5-year overall survival rate was 97% among TEL/AML-positive patients compared with 89% among TEL/AML1-negative patients (P = .03). However, in a multivariable analysis, risk group (age and leukocyte count at diagnosis) and asparaginase treatment group, but not TEL/AML1 status, were found to be independent predictors of outcome. We conclude that TEL/AML1-positive patients have excellent outcomes, confirming our previous findings. However, factors such as age at diagnosis and presenting leukocyte count should be taken into consideration when treating this group of patients.

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References
1.
Whitehead V, Vuchich M, Cooley L, Lauer S, Mahoney D, Shuster J . Accumulation of methotrexate polyglutamates, ploidy and trisomies of both chromosomes 4 and 10 in lymphoblasts from children with B-progenitor cell acute lymphoblastic leukemia: a Pediatric Oncology Group Study. Leuk Lymphoma. 1999; 31(5-6):507-19. DOI: 10.3109/10428199809057610. View

2.
Loh M, Silverman L, Young M, Neuberg D, Golub T, Sallan S . Incidence of TEL/AML1 fusion in children with relapsed acute lymphoblastic leukemia. Blood. 1998; 92(12):4792-7. View

3.
Wiemels J, Cazzaniga G, Daniotti M, Eden O, Addison G, Masera G . Prenatal origin of acute lymphoblastic leukaemia in children. Lancet. 1999; 354(9189):1499-503. DOI: 10.1016/s0140-6736(99)09403-9. View

4.
Arico M, Valsecchi M, Camitta B, Schrappe M, Chessells J, Baruchel A . Outcome of treatment in children with Philadelphia chromosome-positive acute lymphoblastic leukemia. N Engl J Med. 2000; 342(14):998-1006. DOI: 10.1056/NEJM200004063421402. View

5.
Ramakers-Van Woerden N, Pieters R, Loonen A, Hubeek I, van Drunen E, Beverloo H . TEL/AML1 gene fusion is related to in vitro drug sensitivity for L-asparaginase in childhood acute lymphoblastic leukemia. Blood. 2000; 96(3):1094-9. View