Clinical significance of minimal residual disease in childhood acute lymphoblastic leukemia after first relapse

被引:89
作者
Coustan-Smith, E
Gajjar, A
Hijiya, N
Razzouk, BI
Ribeiro, RC
Rivera, GK
Rubnitz, JE
Sandlund, JT
Andreansky, M
Hancock, ML
Pui, CH
Campana, D
机构
[1] Childrens Res Hosp, Dept Hematol Oncol, Memphis, TN USA
[2] St Jude Childrens Res Hosp, Dept Biostat, Memphis, TN 38105 USA
[3] Childrens Res Hosp, Dept Pathol, Memphis, TN USA
[4] Univ Tennessee, Ctr Hlth Sci, Memphis, TN 38163 USA
关键词
acute lymphoblastic leukemia; minimal residual disease; relapse; flow cytometry;
D O I
10.1038/sj.leu.2403283
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Using flow cytometric techniques capable of detecting 0.01% leukemic cells, we prospectively studied minimal residual disease (MRD) in patients with acute lymphoblastic leukemia (ALL) after first relapse. At the end of remission reinduction, 41 patients had a bone marrow sample adequate for MRD studies; 35 of these were in morphologic remission. Of the 35 patients, 19 (54%) had MRD greater than or equal to0.01%, a finding that was associated with subsequent leukemia relapse. The 2-year cumulative incidence of second leukemia relapse was 70.2 +/- 12.3% for the 19 MRD-positive patients and 27.9 +/- 12.4% for the 16 MRD-negative patients ( P = 0.008). Among patients with a first relapse off therapy, 2-year second relapse rates were 49.1 +/- 17.8% in the 12 MRD-positive and 0% in the 11 MRD-negative patients ( P = 0.014); among those who received only chemotherapy after first relapse, the 2-year second relapse rates were 81.5 +/- 14.4% ( n = 12) and 25.0 +/- 13.1% ( n = 13), respectively ( P = 0.004). Time of first relapse and MRD were the only two significant predictors of outcome in a multivariate analysis. We conclude that MRD assays should be used to guide the selection of postremission therapy in patients with ALL in first relapse.
引用
收藏
页码:499 / 504
页数:6
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