Absence of Biallelic TCR gamma Deletion Predicts Early Treatment Failure in Pediatric T-Cell Acute Lymphoblastic Leukemia

作者:Gutierrez Alejandro; Dahlberg Suzanne E; Neuberg Donna S; Zhang Jianhua; Grebliunaite Ruta; Sanda Takaomi; Protopopov Alexei; Tosello Valeria; Kutok Jeffery; Larson Richard S; Borowitz Michael J; Loh Mignon L; Ferrando Adolfo A; Winter Stuart S; Mullighan Charles G; Silverman Lewis B; Chin Lynda; Hunger Stephen P; Sallan Stephen E; Look A Thomas*
来源:Journal of Clinical Oncology, 2010, 28(24): 3816-3823.
DOI:10.1200/JCO.2010.28.3390

摘要

Purpose To identify children with T-cell acute lymphoblastic leukemia (T-ALL) at high risk of induction chemotherapy failure by using DNA copy number analysis of leukemic cells collected at diagnosis. Patients and Methods Array comparative genomic hybridization (CGH) was performed on genomic DNA extracted from diagnostic lymphoblasts from 47 children with T-ALL treated on Children's Oncology Group Study P9404 or Dana-Farber Cancer Institute Protocol 00-01. These samples represented nine patients who did not achieve an initial complete remission, 13 who relapsed, and 25 who became long-term, event-free survivors. The findings were confirmed in an independent cohort of patients by quantitative DNA polymerase chain reaction (DNA-PCR), an assay that is well suited for clinical application. Results Analysis of the CGH findings in patients in whom induction chemotherapy failed compared with those in whom induction chemotherapy was successful identified the absence of biallelic TCR gamma locus deletion (ABD), a characteristic of early thymocyte precursors before V(D)J recombination, as the most robust predictor of induction failure (P < .001). This feature was also associated with markedly inferior event-free (P = .002) and overall survival (P < .001) rates: 25% versus 58% and 25% versus 72%, respectively. Using a rapid and inexpensive quantitative DNA-PCR assay, we validated ABD as a predictor of a poor response to induction chemotherapy in an independent series of patients. Conclusion Lymphoblasts from children with T-ALL should be evaluated at diagnosis for deletion within the TCR gamma locus. Patients lacking biallelic deletion, which confers a high probability of induction failure with contemporary therapy, should be assigned to alternative therapy in the context of a prospective clinical trial.

  • 出版日期2010-8-20