Case-control study suggests a favorable impact of TEL rearrangement in patients with B-lineage acute lymphoblastic leukemia treated with antimetabolite-based therapy: a Pediatric Oncology Group study
Autor: | J E, Rubnitz, J J, Shuster, V J, Land, M P, Link, D J, Pullen, B M, Camitta, C H, Pui, J R, Downing, F G, Behm |
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Rok vydání: | 1997 |
Předmět: |
Male
Antimetabolites Antineoplastic Hydrocortisone Oncogene Proteins Fusion Chromosomes Human Pair 21 Translocation Genetic Antineoplastic Combined Chemotherapy Protocols Biomarkers Tumor Asparaginase Humans Single-Blind Method Child Retrospective Studies Chromosomes Human Pair 12 Mercaptopurine Remission Induction Cytarabine DNA Neoplasm Prognosis Burkitt Lymphoma Neoplasm Proteins Blotting Southern Methotrexate Treatment Outcome Vincristine Case-Control Studies Core Binding Factor Alpha 2 Subunit Prednisone Female |
Zdroj: | Blood. 89(4) |
ISSN: | 0006-4971 |
Popis: | TEL gene rearrangement is the most common genetic lesion in pediatric acute lymphoblastic leukemia (ALL), occurring in about 25% of B-lineage cases. We previously showed that, among patients treated on St Jude protocols, TEL rearrangement independently conferred an excellent prognosis. To extend these results to patients treated with antimetabolite-based therapy, we performed Southern blot analysis to determine the TEL gene status of 104 cases of B-lineage ALL treated on Pediatric Oncology Group 8602, matched on age, gender, and leukocyte count. There were 52 failures among the 77 patients with germline TEL, compared with only 8 failures among 27 patients in the rearranged group. Based on a two-sided logistic regression analysis, stratified for age (subdivided at 10 years), leukocyte count (subdivided at 50,000), and gender, the estimated odds of failing by 4 years in the germline TEL group is 5.4 times that of the rearranged TEL group, with 95% confidence from 1.9 to 15.6, two-sided P = .0009. Thus, the presence of a rearranged TEL gene is also associated with an improved survival among patients treated with antimetabolite-based therapy. Our results indicate that all newly diagnosed ALL patients should be screened for TEL gene rearrangements and suggest that these patients are candidates for less intensive therapy. |
Databáze: | OpenAIRE |
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