Gene-Expression Patterns in Drug-Resistant Acute Lymphoblastic Leukemia Cells and Response to Treatment

Amy de Haar-Holleman(Erasmus MC), Meyling Cheok(St. Jude Children's Research Hospital), Monique L. den Boer(Erasmus MC - Sophia Children’s Hospital), Wenjian Yang(St. Jude Children's Research Hospital), Anjo J.P. Veerman(University Medical Center), Karin M. Kazemier(Erasmus MC - Sophia Children’s Hospital), Deqing Pei(St. Jude Children's Research Hospital), Cheng Cheng(St. Jude Children's Research Hospital), Ching‐Hon Pui(St. Jude Children's Research Hospital), Mary V. Relling(St. Jude Children's Research Hospital), Gritta Janka‐Schaub(Kinderkrebs-Zentrum Hamburg), Rob Pieters(Erasmus MC - Sophia Children’s Hospital), William E. Evans(St. Jude Children's Research Hospital)
New England Journal of Medicine
August 4, 2004
Cited by 644Open Access
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Abstract

BACKGROUND: Childhood acute lymphoblastic leukemia (ALL) is curable with chemotherapy in approximately 80 percent of patients. However, the cause of treatment failure in the remaining 20 percent of patients is largely unknown. METHODS: We tested leukemia cells from 173 children for sensitivity in vitro to prednisolone, vincristine, asparaginase, and daunorubicin. The cells were then subjected to an assessment of gene expression with the use of 14,500 probe sets to identify differentially expressed genes in drug-sensitive and drug-resistant ALL. Gene-expression patterns that differed according to sensitivity or resistance to the four drugs were compared with treatment outcome in the original 173 patients and an independent cohort of 98 children treated with the same drugs at another institution. RESULTS: We identified sets of differentially expressed genes in B-lineage ALL that were sensitive or resistant to prednisolone (33 genes), vincristine (40 genes), asparaginase (35 genes), or daunorubicin (20 genes). A combined gene-expression score of resistance to the four drugs, as compared with sensitivity to the four, was significantly and independently related to treatment outcome in a multivariate analysis (hazard ratio for relapse, 3.0; P=0.027). Results were confirmed in an independent population of patients treated with the same medications (hazard ratio for relapse, 11.85; P=0.019). Of the 124 genes identified, 121 have not previously been associated with resistance to the four drugs we tested. CONCLUSIONS: Differential expression of a relatively small number of genes is associated with drug resistance and treatment outcome in childhood ALL.


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