Risk-adapted treatment according to minimal residual disease in adult ALL

被引:12
作者
Gökbuget, N
Kneba, M
Raff, T
Bruggemann, M
Scheuring, U
Reutzel, R
Hoelzer, D
机构
[1] JW Goethe Univ Hosp, Med Clin 3, D-60590 Frankfurt, Germany
[2] Univ Kiel, Med Clin & Policlin 2, D-24116 Kiel, Germany
关键词
minimal residual disease; acute lymphoblastic leukaemia; prognostic factors;
D O I
10.1053/beha.2002.0229
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The evaluation of minimal residual disease (MRD) is a new diagnostic method which is applicable in various malignant disorders. Acute lymphoblastic leukaemia (ALL) is a somewhat ideal disease in this respect because >90% of the patients show individual clonal markers and because several methods for MRD evaluation are already established. Futhermore, it was demonstrated that level and course of MRD are significantly correlated with relapse risk in childhood and in adult ALL. In clinical practice MRD evaluation may serve for several purposes such as follow-up ofindividual course of disease, identification of new prognostic factors or evaluation of single treatment elements. We discuss these options as well as general considerations for MRD-based risk stratification and treatment options for risk groups. Practical applications are analysed because prospective MRD-based clinical trials have been recently started. Finally, future options for application of MRD evaluation and also limitations and pitfalls of this method are reviewed.
引用
收藏
页码:639 / 652
页数:14
相关论文
共 42 条
[1]   Treatment of adult acute lymphoblastic leukemia (ALL): long-term follow-up of the GIMEMA ALL 0288 randomized study [J].
Annino, L ;
Vegna, ML ;
Camera, A ;
Specchia, G ;
Visani, G ;
Fioritoni, G ;
Ferrara, F ;
Peta, A ;
Ciolli, S ;
Deplano, W ;
Fabbiano, F ;
Sica, S ;
Di Raimondo, F ;
Cascavilla, N ;
Tabilio, A ;
Leoni, P ;
Invernizzi, R ;
Baccarani, M ;
Rotoli, B ;
Amadori, S ;
Mandelli, F .
BLOOD, 2002, 99 (03) :863-871
[2]   Purging in BCR-ABL-positive acute lymphoblastic leukemia using immunomagnetic beads:: comparison of residual leukemia and purging efficiency in bone marrow vs peripheral blood stem cells by semiquantitative polymerase chain reaction [J].
Atta, J ;
Fauth, F ;
Keyser, M ;
Petershofen, E ;
Weber, C ;
Lippok, G ;
Hoelzer, D ;
Martin, H .
BONE MARROW TRANSPLANTATION, 2000, 25 (01) :97-104
[3]   Monitoring minimal residual disease in peripheral blood in B-lineage acute lymphoblastic leukaemia [J].
Brisco, MJ ;
Sykes, PJ ;
Hughes, E ;
Dolman, G ;
Neoh, SH ;
Peng, LM ;
Toogood, I ;
Morley, AA .
BRITISH JOURNAL OF HAEMATOLOGY, 1997, 99 (02) :314-319
[4]   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
[5]  
BRUEGGEMANN M, 2001, HEMATOL J, V1, pA700
[6]  
Brüggemann M, 2001, BLOOD, V98, p314A
[7]  
Cimino G, 2000, BLOOD, V95, P96
[8]   Prognostic value of immunophenotypic detection of minimal residual disease in acute lymphoblastic leukemia [J].
Ciudad, J ;
San Miguel, JF ;
López-Berges, MC ;
Vidriales, B ;
Valverde, B ;
Ocqueteau, M ;
Mateos, G ;
Caballero, MD ;
Hernández, J ;
Moro, MJ ;
Mateos, MV ;
Orfao, A .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (12) :3774-3781
[9]   Use of peripheral blood instead of bone marrow to monitor residual disease in children with acute lymphoblastic leukemia [J].
Coustan-Smith, E ;
Sancho, J ;
Hancock, ML ;
Razzouk, BI ;
Ribeiro, RC ;
Rivera, GK ;
Rubnitz, JE ;
Sandlund, JT ;
Pui, CH ;
Campana, D .
BLOOD, 2002, 100 (07) :2399-2402
[10]   Detection of minimal residual disease:: Methods and relationship to outcome in T-lineage acute lymphoblastic leukemia [J].
Dibenedetto, SP ;
Lo Nigro, L ;
Di Cataldo, A ;
Schilirò, G .
LEUKEMIA & LYMPHOMA, 1998, 32 (1-2) :65-75