Molecular detection of minimal residual disease in adult and childhood acute lymphoblastic leukaemia reveals differences in treatment response

被引:64
作者
Foroni, L [1 ]
Coyle, LA [1 ]
Papaioannou, M [1 ]
Yaxley, JC [1 ]
Sinclair, MFC [1 ]
Chim, JS [1 ]
Cannell, P [1 ]
SeckerWalker, LM [1 ]
Mehta, AB [1 ]
Prentice, HG [1 ]
Hoffbrand, AV [1 ]
机构
[1] UNIV LONDON SCH MED,LONDON NW3 2QG,ENGLAND
基金
英国医学研究理事会;
关键词
MRD; ALL; CDR3;
D O I
10.1038/sj.leu.2400841
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Immunoglobulin heavy chain gene (IgH gene) rearrangements are found in the majority of patients with B lineage acute lymphoblastic leukaemia (ALL). Two hundred and three bone marrow samples from 54 patients (33 adults and 21 children) were analysed by PCR within specific time-points after diagnosis tie 1, 2-3, 4-6 and 7-12 months) using FR1 and JH primers (fingerprinting with a sensitivity greater than or equal to 1:5x10(3)). CDR3-derived allele specific oligoprimers (ASO to achieve a sensitivity between 1:10(4) and 1:10(5)) were applied to 12 children and 18 adults, while size of CDR3 region, oligoclonality and background problems prevented their application to the remaining patients. All patients were followed clinically for greater than or equal to 24 months. Thirty adults and 16 children presented as newly diagnosed ALL, while the remaining eight patients were analysed in first or subsequent relapse. Patients destined to relapse showed a higher proportion of positive tests (greater than or equal to 50%), particularly after 1 month, than in the remission group, irrespective of age. Among patients staying in remission, a decrease in MRD-positive tests occurred during the first 12 months in both age groups. However, the proportion of positive tests dropped below 15% at a later stage in adults (4-6 months) than in children (2-3 months). Among children, only patients destined to relapse were BARD positive beyond 1 month, with the exception of only one patient, still positive at 2-3 months in the remission group. The difference in MRD positivity between relapse and remission patients was statistically significant in children (P < 0.03) at any time of testing, but only at 4-6 months in adults (P < 0.01). These data suggest that resolution of MRD in ALL occurs more rapidly in children compared to adults, particularly within the first 6 months. Children and adults, studied in first or subsequent relapse, showed a higher proportion of positive tests during reinduction compared to newly diagnosed patients.
引用
收藏
页码:1732 / 1741
页数:10
相关论文
共 34 条
[1]  
BARTRAM CR, 1992, BRIT J HAEMATOL, V82, P182
[2]   CONTENT AND ORGANIZATION OF THE HUMAN IG VH LOCUS - DEFINITION OF 3 NEW VH FAMILIES AND LINKAGE TO THE IG CH LOCUS [J].
BERMAN, JE ;
MELLIS, SJ ;
POLLOCK, R ;
SMITH, CL ;
SUH, H ;
HEINKE, B ;
KOWAL, C ;
SURTI, U ;
CHESS, L ;
CANTOR, CR ;
ALT, FW .
EMBO JOURNAL, 1988, 7 (03) :727-738
[3]  
BIONDI A, 1992, LEUKEMIA, V6, P282
[4]   DETECTION AND QUANTITATION OF NEOPLASTIC-CELLS IN ACUTE LYMPHOBLASTIC-LEUKEMIA, BY USE OF THE POLYMERASE CHAIN-REACTION [J].
BRISCO, MJ ;
CONDON, J ;
SYKES, PJ ;
NEOH, SH ;
MORLEY, AA .
BRITISH JOURNAL OF HAEMATOLOGY, 1991, 79 (02) :211-217
[5]  
BRISCO MJ, 1993, LEUKEMIA, V7, P1514
[6]   OUTCOME PREDICTION IN CHILDHOOD ACUTE LYMPHOBLASTIC-LEUKEMIA BY MOLECULAR QUANTIFICATION OF RESIDUAL DISEASE AT THE END OF INDUCTION [J].
BRISCO, MJ ;
CONDON, J ;
HUGHES, E ;
NEOH, SH ;
SYKES, PJ ;
SESHADRI, R ;
TOOGOOD, I ;
WATERS, K ;
TAURO, G ;
EKERT, H ;
MORLEY, AA .
LANCET, 1994, 343 (8891) :196-200
[7]   Relationship between minimal residual disease and outcome in adult acute lymphoblastic leukemia [J].
Brisco, MJ ;
Hughes, E ;
Neoh, SH ;
Sykes, PJ ;
Bradstock, K ;
Enno, A ;
Szer, J ;
McCaul, K ;
Morley, AA .
BLOOD, 1996, 87 (12) :5251-5256
[8]   THE USE OF CHROMOSOMAL TRANSLOCATIONS TO STUDY HUMAN-IMMUNOGLOBULIN GENE ORGANIZATION - MAPPING DH SEGMENTS WITHIN 35 KB OF THE C-MU GENE AND IDENTIFICATION OF A NEW DH LOCUS [J].
BULUWELA, L ;
ALBERTSON, DG ;
SHERRINGTON, P ;
RABBITTS, PH ;
SPURR, N ;
RABBITTS, TH .
EMBO JOURNAL, 1988, 7 (07) :2003-2010
[9]  
Campana D, 1990, Baillieres Clin Haematol, V3, P889, DOI 10.1016/S0950-3536(05)80140-4
[10]  
CAVE H, 1994, BLOOD, V83, P1892