Prognostic Value of Minimal Residual Disease Quantification Before Allogeneic Stem-Cell Transplantation in Relapsed Childhood Acute Lymphoblastic Leukemia: The ALL-REZ BFM Study Group

被引:284
作者
Bader, Peter
Kreyenberg, Hermann
Henze, Guenter H. R.
Eckert, Cornelia
Reising, Miriam
Willasch, Andre
Barth, Andrea
Borkhardt, Arndt
Peters, Christina
Handgretinger, Rupert
Sykora, Karl-Walter
Holter, Wolfgang
Kabisch, Hartmut
Klingebiel, Thomas
von Stackelberg, Arend
机构
[1] Goethe Univ Frankfurt, Childrens Hosp, Frankfurt, Germany
[2] Charite, Berlin, Germany
[3] Univ Med Ctr, Dusseldorf, Germany
[4] Univ Childrens Hosp Tubingen, Tubingen, Germany
[5] Hannover Med Sch, D-30623 Hannover, Germany
[6] Univ Childrens Hosp, Erlangen, Germany
[7] Univ Childrens Hosp Hamburg, Hamburg, Germany
[8] St Anna Childrens Hosp, Vienna, Austria
关键词
TIME QUANTITATIVE PCR; BONE-MARROW-TRANSPLANTATION; VERSUS-HOST-DISEASE; GENE REARRANGEMENTS; PEDIATRIC-PATIENTS; CHILDREN; CHIMERISM; MRD; CHEMOTHERAPY; METHOTREXATE;
D O I
10.1200/JCO.2008.17.6065
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Minimal residual disease (MRD) before allogeneic stem-cell transplantation was shown to predict outcome in children with relapsed acute lymphoblastic leukemia (ALL) in retrospective analysis. To verify this, the Acute Lymphoblastic Leukemia Relapse Berlin-Frankfurt- Munster (ALL-REZ BFM) Study Group conducted a prospective trial. Patients and Methods Between March 1999 and July 2005, 91 children with relapsed ALL treated according to the ALL-REZ BFM 96 or 2002 protocols and receiving stem-cell transplantation in >= second remission were enrolled. MRD quantification was performed by real-time polymerase chain reaction using T-cell receptor and immunoglobulin gene rearrangements. Results Probability of event-free survival (pEFS) and cumulative incidence of relapse (CIR) in 45 patients with MRD >= 10(-4) leukemic cells was 0.27 and 0.57 compared with 0.60 and 0.13 in 46 patients with MRD less than 10(-4) leukemic cells (EFS, P = .004; CIR, P < .001). Intermediate-risk patients (strategic group S1) with MRD >= 10(-4) leukemic cells (n = 14) had a pEFS of 0.20 and CIR of 0.73, whereas patients with MRD less than 10(-4) leukemic cells (n = 21) had a pEFS of 0.68 and CIR of 0.09 (EFS, P = .020; CIR, P < .001). High-risk patients (S3/4, third complete remission) who received transplantation with an MRD load of less than 10(-4) leukemic cells (n = 25) showed a pEFS and CRI of 0.53 and 0.18, respectively. In contrast, pEFS and CRI were 0.30 and 0.50 in patients who received transplantation with an MRD load of >= 10(-4) leukemic cells. Multivariate Cox regression analysis revealed MRD as the only independent parameter predictive for EFS (P = .006). Conclusion MRD is an important predictor for post-transplantation outcome. As a result, new strategies with modified stem-cell transplantation procedures will be evaluated in ALL-BFM trials.
引用
收藏
页码:377 / 384
页数:8
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