Quantification of minimal residual disease in T-lineage acute lymphoblastic leukemia with the TAL-1 deletion using a standardized real-time PCR assay

Hematologic relapse remains the greatest obstacle to the cure of children with acute lymphoblastic leukemia (ALL), Recent studies have shown that patients with increased risk of relapse can be identified by measuring residual leukemic cells, called minimal residual disease (MRD), during clinical remission. Current PCR methods, however, for measuring MRD are cumbersome and time-consuming. To improve and simplify MRD assessment, we developed a real-time quantitative PCR (RQ-PCR) assay for detection of leukemic cells that harbor the TAL-1 deletion. We studied serial dilutions of leukemic DNA and found the assay had a sensitivity of detection of one leukemic cell among 100 000 normal cells. We then investigated 23 samples from eight children with ALL in clinical remission. We quantified residual leukemic cells by using the TAL-I RQ-PCR assay and by using limiting dilution analysis. In 17 samples, both methods detected MRD levels greater than or equal to0.001%. The percentages of leukemic cells measured by the two methods correlated well (r(2) = 0.926), In the remaining six samples, both methods detected fewer than 0.001% leukemic cells. We conclude the TAL-I RQ-PCR assay can be used for rapid, sensitive and accurate assessment of MRD in T-lineage ALL with the TAL-I deletion.