Molecular monitoring of BCR-ABL as a guide to clinical management in chronic myeloid leukaemia

被引:105
作者
Hughes, T
Branford, S
机构
[1] Inst Med & Vet Sci, Adelaide, SA 5000, Australia
[2] Univ Adelaide, Adelaide, SA 5000, Australia
关键词
chronic myeloid leukaemia; imatinib; RQ-PCR; BCR-ABL; molecular monitoring;
D O I
10.1016/j.blre.2005.01.008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Molecular monitoring of BCR-ABL transcript levels by real-time quantitative PCR is increasingly used to assess treatment response in patients with chronic myeloid leukaemia (CML). This has become particularly relevant in the era of imatinib therapy when residual levels of leukaemia usually fall below the level of detection by bone marrow cytogenetic analysis. Studies of imatinib-treated patients have determined that BCR-ABL levels measured early in therapy can predict subsequent response and the probability of acquired resistance. The defining of a molecular level of response that indicates a high probability of progression-free survival highlights the relevance of molecular analysis for clinical management. Small increases in the BCR-ABL level can identify patients with kinase domain mutations that lead to imatinib resistance. Therefore, these assays can be used as a screening strategy for mutation analysis. As second generation kinase inhibitors commence clinical trials, the molecular response will be a primary end-point that determines efficacy. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:29 / 41
页数:13
相关论文
共 93 条
[1]   High incidence of BCR-ABL kinase domain mutations and absence of mutations of the PDGFR and KIT activation loops in CML patients with secondary resistance to imatinib [J].
Al-Ali, HK ;
Heinrich, MC ;
Lange, T ;
Krahl, R ;
Mueller, M ;
Müller, C ;
Niederwieser, D ;
Druker, BJ ;
Deininger, MWN .
HEMATOLOGY JOURNAL, 2004, 5 (01) :55-60
[2]  
Barbany G, 2000, CLIN CHEM, V46, P913
[3]   THE CHRONIC MYELOGENOUS LEUKEMIA SPECIFIC P210-PROTEIN IS THE PRODUCT OF THE BCR/ABL HYBRID GENE [J].
BEN-NERIAH, Y ;
DALEY, GQ ;
MESMASSON, AM ;
WITTE, ON ;
BALTIMORE, D .
SCIENCE, 1986, 233 (4760) :212-214
[4]   Chronic myeloid leukemia and interferon-α:: a study of complete cytogenetic responders [J].
Bonifazi, F ;
de Vivo, A ;
Rosti, G ;
Guilhot, F ;
Guilhot, J ;
Trabacchi, E ;
Hehlmann, R ;
Hochhaus, A ;
Shepherd, PCA ;
Steegmann, JL ;
Kluin-Nelemans, HC ;
Thaler, J ;
Simonsson, B ;
Louwagie, A ;
Reiffers, J ;
Mahon, FX ;
Montefusco, E ;
Alimena, G ;
Hasford, J ;
Richards, S ;
Saglio, G ;
Testoni, N ;
Martinelli, G ;
Tura, S ;
Baccarani, M .
BLOOD, 2001, 98 (10) :3074-3081
[5]   High frequency of point mutations clustered within the adenosine triphosphate-binding region of BCR/ABL in patients with chronic myeloid leukemia or Ph-positive acute lymphoblastic leukemia who develop imatinib (STI571) resistance [J].
Branford, S ;
Rudzki, Z ;
Walsh, S ;
Grigg, A ;
Arthur, C ;
Taylor, K ;
Herrmann, R ;
Lynch, KP ;
Hughes, TP .
BLOOD, 2002, 99 (09) :3472-3475
[6]   Detection of BCR-ABL mutations in patients with CML treated with imatinib is virtually always accompanied by clinical resistance, and mutations in the ATP phosphate-binding loop (P-loop) are associated with a poor prognosis [J].
Branford, S ;
Rudzki, Z ;
Walsh, S ;
Parkinson, I ;
Grigg, A ;
Szer, J ;
Taylor, K ;
Herrmann, R ;
Seymour, JF ;
Arthur, C ;
Joske, D ;
Lynch, K ;
Hughes, T .
BLOOD, 2003, 102 (01) :276-283
[7]   Real-time quantitative PCR analysis can be used as a primary screen to identify patients with CML treated with imatinib who have BCR-ABL kinase domain mutations [J].
Branford, S ;
Rudzki, Z ;
Parkinson, I ;
Grigg, A ;
Taylor, K ;
Seymour, JF ;
Durrant, S ;
Browett, P ;
Schwarer, AP ;
Arthur, C ;
Catalano, J ;
Leahy, MF ;
Filshie, R ;
Bradstock, K ;
Herrmann, R ;
Joske, D ;
Lynch, K ;
Hughes, T .
BLOOD, 2004, 104 (09) :2926-2932
[8]   Imatinib produces significantly superior molecular responses compared to interferon alfa plus cytarabine in patients with newly diagnosed chronic myeloid leukemia in chronic phase [J].
Branford, S ;
Rudzki, Z ;
Harper, A ;
Grigg, A ;
Taylor, K ;
Durrant, S ;
Arthur, C ;
Browett, P ;
Schwarer, AP ;
Ma, D ;
Seymour, JF ;
Bradstock, K ;
Joske, D ;
Lynch, K ;
Gathmann, I ;
Hughes, TP .
LEUKEMIA, 2003, 17 (12) :2401-2409
[9]  
Branford S, 1999, BRIT J HAEMATOL, V107, P587
[10]  
Branford S, 2003, BLOOD, V102, p414A