Minimal residual disease analysis by eight-color flow cytometry in relapsed childhood acute lymphoblastic leukemia

被引:55
作者
Karawajew, Leonid [1 ]
Dworzak, Michael [2 ,3 ]
Ratei, Richard [4 ]
Rhein, Peter [1 ]
Gaipa, Giuseppe [5 ]
Buldini, Barbara [6 ]
Basso, Giuseppe [6 ]
Hrusak, Ondrej [7 ,8 ]
Ludwig, Wolf-Dieter [4 ]
Henze, Guenter [1 ]
Seeger, Karl [1 ]
von Stackelberg, Arend [1 ]
Mejstrikova, Ester [7 ,8 ]
Eckert, Cornelia [1 ]
机构
[1] Charite, Dept Pediat Oncol Hematol, D-13353 Berlin, Germany
[2] Med Univ Vienna, St Anna Childrens Hosp, Vienna, Austria
[3] Med Univ Vienna, Childrens Canc Res Inst, Dept Pediat, Vienna, Austria
[4] HELIOS Klin, Robert Roessle Clin, Berlin, Germany
[5] Univ Milano Bicocca, Dept Pediat, Tettamanti Res Ctr, Osped San Gerardo, Monza, Italy
[6] Univ Hosp Padova, Dept Pediat, Lab Pediat Oncohematol, Padua, Italy
[7] Charles Univ Prague, Dept Pediat Hematol & Oncol, Fac Med 2, Prague, Czech Republic
[8] Univ Hosp Motol, Prague, Czech Republic
关键词
PRECURSOR-B-ALL; CLINICAL-SIGNIFICANCE; AIEOP-BFM; PROGNOSTIC-SIGNIFICANCE; GENE REARRANGEMENTS; INDUCTION THERAPY; PREDICTIVE FACTOR; QUANTITATIVE PCR; MARROW RELAPSE; BONE-MARROW;
D O I
10.3324/haematol.2014.116707
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Multiparametric flow cytometry is an alternative approach to the polymerase chain reaction method for evaluating minimal residual disease in treatment protocols for primary acute lymphoblastic leukemia. Given considerable differences between primary and relapsed acute lymphoblastic leukemia treatment regimens, flow cytometric assessment of minimal residual disease in relapsed leukemia requires an independent comprehensive investigation. In the present study we addressed evaluation of minimal residual disease by flow cytometry in the clinical trial for childhood relapsed acute lymphoblastic leukemia using eight-color flow cytometry. The major challenge of the study was to reliably identify low amounts of residual leukemic cells against the complex background of regeneration, characteristic of follow-up samples during relapse treatment. In a prospective study of 263 follow-up bone marrow samples from 122 patients with B-cell precursor acute lymphoblastic leukemia, we tested various B-cell markers, adapted the antibody panel to the treatment protocol, and evaluated its performance by a blinded parallel comparison with the polymerase chain reaction data. The resulting eight-color single-tube panel showed a consistently high overall concordance (P<0.001) and, under optimal conditions, sensitivity similar to that of the reference polymerase chain reaction method. Overall, evaluation of minimal residual disease by flow cytometry can be successfully integrated into the clinical management of relapsed childhood acute lymphoblastic leukemia either as complementary to the polymerase chain reaction or as an independent risk stratification tool. ALL-REZ BFM 2002 clinical trial information: NCT00114348
引用
收藏
页码:935 / 944
页数:10
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[1]   Minimal residual disease values discriminate between low and high relapse risk in children with B-cell precursor acute lymphoblastic leukemia and an intrachromosomal amplification of chromosome 21: The Austrian and German acute lymphoblastic leukemia Berlin-Frankfurt-Munster (ALL-BFM) trials [J].
Attarbaschi, Andishe ;
Mann, Georg ;
Panzer-Gruemayer, Renate ;
Roettgers, Silja ;
Steiner, Manuel ;
Koenig, Margit ;
Csinady, Eva ;
Dworzak, Michael N. ;
Seidel, Markus ;
Janousek, Dasa ;
Moericke, Anja ;
Reichelt, Carsten ;
Harbott, Jochen ;
Schrappe, Martin ;
Gadner, Helmut ;
Haas, Oskar A. .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (18) :3046-3050
[2]   Risk of Relapse of Childhood Acute Lymphoblastic Leukemia Is Predicted By Flow Cytometric Measurement of Residual Disease on Day 15 Bone Marrow [J].
Basso, Giuseppe ;
Veltroni, Marinella ;
Valsecchi, Maria Grazia ;
Dworzak, Michael N. ;
Ratei, Richard ;
Silvestri, Daniela ;
Benetello, Alessandra ;
Buldini, Barbara ;
Maglia, Oscar ;
Masera, Giuseppe ;
Conter, Valentino ;
Arico, Maurizio ;
Biondi, Andrea ;
Gaipa, Giuseppe .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (31) :5168-5174
[3]   Molecular detection of minimal residual disease is a strong predictive factor of relapse in childhood B-lineage acute lymphoblastic leukemia with medium risk features.: A case control study of the International BFM study group [J].
Biondi, A ;
Valsecchi, MG ;
Seriu, T ;
D'Aniello, E ;
Willemse, MJ ;
Fasching, K ;
Pannunzio, A ;
Gadner, H ;
Schrappe, M ;
Kamps, WA ;
Bartram, CR ;
van Dongen, JJM ;
Panzer-Grümayer, ER .
LEUKEMIA, 2000, 14 (11) :1939-1943
[4]   STATISTICAL METHODS FOR ASSESSING AGREEMENT BETWEEN TWO METHODS OF CLINICAL MEASUREMENT [J].
BLAND, JM ;
ALTMAN, DG .
LANCET, 1986, 1 (8476) :307-310
[5]   Clinical significance of minimal residual disease in childhood acute lymphoblastic leukemia and its relationship to other prognostic factors: a Children's Oncology Group study [J].
Borowitz, Michael J. ;
Devidas, Meenakshi ;
Hunger, Stephen P. ;
Bowman, W. Paul ;
Carroll, Andrew J. ;
Carroll, William L. ;
Linda, Stephen ;
Martin, Paul L. ;
Pullen, D. Jeanette ;
Viswanatha, David ;
Willman, Cheryl L. ;
Winick, Naomi ;
Camitta, Bruce M. .
BLOOD, 2008, 111 (12) :5477-5485
[6]   Minimal residual disease detection in childhood precursor-B-cell acute lymphoblastic leukemia: relation to other risk factors. A Children's Oncology Group study [J].
Borowitz, MJ ;
Pullen, DJ ;
Shuster, JJ ;
Viswanatha, D ;
Montgomery, K ;
Willman, CL ;
Camitta, B .
LEUKEMIA, 2003, 17 (08) :1566-1572
[7]   Detection of minimal residual disease in acute lymphoblastic leukemia: the St Jude experience [J].
Campana, D ;
Neale, GAM ;
Coustan-Smith, E ;
Pui, CH .
LEUKEMIA, 2001, 15 (02) :278-279
[8]   Minimal residual disease monitoring in childhood acute lymphoblastic leukemia [J].
Campana, Dario .
CURRENT OPINION IN HEMATOLOGY, 2012, 19 (04) :313-318
[9]   Progress of Minimal Residual Disease Studies in Childhood Acute Leukemia [J].
Campana, Dario .
CURRENT HEMATOLOGIC MALIGNANCY REPORTS, 2010, 5 (03) :169-176
[10]   Clinical significance of minimal residual disease in childhood acute lymphoblastic leukemia [J].
Cavé, H ;
ten Bosch, JV ;
Suciu, S ;
Guidal, C ;
Waterkeyn, C ;
Otten, J ;
Bakkus, M ;
Thielemans, K ;
Grandchamp, B ;
Vilmer, E .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (09) :591-598