NUP214-ABL1 in adult T-ALL:: the GMALL study group experience

被引:39
作者
Burmeister, Thomas
Gokbuget, Nicola
Reinhardt, Richard
Rieder, Harald
Hoelzer, Dieter
Schwartz, Stefan
机构
[1] Charite Univ Med Berlin, Med Klin 3, D-12200 Berlin, Germany
[2] Goethe Univ Frankfurt, Med Klin 3, D-6000 Frankfurt, Germany
[3] Max Planck Inst Mol Genet, Berlin, Germany
[4] Univ Dusseldorf, Inst Humangenet & Anthropol, D-4000 Dusseldorf, Germany
关键词
D O I
10.1182/blood-2006-04-014514
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The NUP214-ABL1 fusion gene in T-cell acute lymphoblastic leukemia (T-ALL) has recently been identified as a possible target for imatinib and related tyrosine kinase inhibitors, but exact data regarding the prognostic impact and frequency of the several putative NUP214-ABL1 mRNA transcripts are still missing. We investigated 279 adult patients with T-ALL treated within the framework of the GMALL 5/93 and 6199 therapy trials for NUP214-ABL1 by using a novel multiplex real-time, quantitative polymerase chain reaction (PCR). Eleven (3.9%) patients were NUP214-ABL1 positive, and 5 different transcripts were observed; 8 patients had a thymic immunophenotype, 1 had an early T-cell immunophenotype, and 2 had a mature T-cell immunophenotype. NUP214-ABL1-positive and -negative patients did not differ significantly in their major clinical features. In contrast to previous reports suggesting an adverse clinical course for NUP214-ABL1-positive patients, no significant difference in overall survival was observed. Based on the results, we have established and tested a novel PCR method for simplified detection of the NUP214-ABL1 fusion gene.
引用
收藏
页码:3556 / 3559
页数:4
相关论文
共 20 条
[1]   NUP214-ABL1 amplification in t(5;14)/HOX11L2-positive ALL present with several forms and may have a prognostic significance [J].
Ballerini, P ;
Busson, M ;
Fasola, S ;
van den Akker, J ;
Lapillonne, H ;
Romana, SP ;
Marynen, P ;
Bernard, OA ;
Landman-Parker, J ;
Berger, R .
LEUKEMIA, 2005, 19 (03) :468-470
[2]   Evaluation of candidate control genes for diagnosis and residual disease detection in leukemic patients using 'real-time' quantitative reverse-transcriptase polymerase chain reaction (RQ-PCR) - a Europe against cancer program [J].
Beillard, E ;
Pallisgaard, N ;
van der Velden, VHJ ;
Bi, W ;
Dee, R ;
van der Schoot, E ;
Delabesse, E ;
Macintyre, E ;
Gottardi, E ;
Saglio, G ;
Watzinger, F ;
Lion, T ;
van Dongen, JJM ;
Hokland, P ;
Gabert, J .
LEUKEMIA, 2003, 17 (12) :2474-2486
[3]   ABL1 amplification in T-cell acute lymphoblastic leukemia [J].
Bernasconi, P ;
Calatroni, S ;
Giardini, I ;
Inzoli, A ;
Castagnola, C ;
Cavigliano, PM ;
Rocca, B ;
Boni, M ;
Quarna, J ;
Zappatore, R ;
Caresana, M ;
Bianchessi, C ;
Pallavicini, EB ;
Lazzarino, M .
CANCER GENETICS AND CYTOGENETICS, 2005, 162 (02) :146-150
[4]  
BRUGGEMANN M, 2005, BLOOD, V107, P2271
[5]   Molecular heterogeneity of sporadic adult Burkitt-type leukemia/lymphoma as revealed by PCR and cytogenetics:: correlation with morphology, immunology and clinical features [J].
Burmeister, T ;
Schwartz, S ;
Horst, HA ;
Rieder, H ;
Gökbuget, N ;
Hoelzer, D ;
Thiel, E .
LEUKEMIA, 2005, 19 (08) :1391-1398
[6]   Fusion of EML1 to ABL1 in T-cell acute lymphoblastic leukemia with cryptic t(9;14)(q34;q32) [J].
De Keersmaecker, K ;
Graux, C ;
Odero, MD ;
Mentens, N ;
Somers, R ;
Maertens, J ;
Wlodarska, I ;
Vandenberghe, P ;
Hagemeijer, A ;
Marynen, P ;
Cools, J .
BLOOD, 2005, 105 (12) :4849-4852
[7]  
Drexler H. G., 2000, LEUKEMIA LYMPHOMA CE
[8]  
FORNEROD M, 1995, ONCOGENE, V10, P1739
[9]  
GALILI U, 1984, CANCER RES, V44, P4594
[10]   Leading prognostic relevance of the BCR-ABL translocation in adult acute B-lineage lymphoblastic leukemia:: a prospective study of the German Multicenter Trial Group and confirmed polymerase chain reaction analysis [J].
Gleissner, B ;
Gökbuget, N ;
Bartram, CR ;
Janssen, B ;
Rieder, H ;
Janssen, JWG ;
Fonatsch, C ;
Heyll, A ;
Voliotis, D ;
Beck, J ;
Lipp, T ;
Munzert, G ;
Maurer, J ;
Hoelzer, D ;
Thiel, E .
BLOOD, 2002, 99 (05) :1536-1543