Deletions at 11q identify a subset of patients with typical CLL who show consistent disease progression and reduced survival

被引:90
作者
Neilson, JR
Auer, R
White, D
Bienz, N
Waters, JJ
Whittaker, JA
Milligan, DW
Fegan, CD
机构
[1] BIRMINGHAM HEARTLANDS HOSP,DEPT HAEMATOL,BIRMINGHAM B9 5SS,W MIDLANDS,ENGLAND
[2] BIRMINGHAM HEARTLANDS HOSP,CYTOGENET LABS,BIRMINGHAM B9 5SS,W MIDLANDS,ENGLAND
[3] UNIV WALES HOSP,CARDIFF CF4 4XW,S GLAM,WALES
关键词
CLL; del(11q); prognosis;
D O I
10.1038/sj.leu.2400819
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Eighty-four patients with typical chronic lymphocytic leukemia (CLL) (by morphological and immunophenotypic criteria) on whom karyotypes were available were studied. Binet stage at diagnosis and follow-up were defined. Survival was calculated from diagnosis. Fifty-one percent of patients had a karyotypic abnormality, the commonest being abnormalities at 13q14 (16%); these patients did not have significantly different survival from patients with normal karyotype. The second commonest abnormality was del(11q) (13%); these patients had significantly worse survival when compared both with patients with normal karyotype (P < 0.0001) and with other patients with karyotypic abnormality (P = 0.0012). All patients with del(11q) had progressed to stage C at follow-up while only 20% of the other patients had shown any disease progression (P < 0.0001). Del(11q) may identify a subset of patients with typical CLL who have worse survival and consistent disease progression and in future may help define a group of patients with CLL who could benefit from earlier or more intensive therapy.
引用
收藏
页码:1929 / 1932
页数:4
相关论文
共 19 条
[1]   TRISOMY-12 IS UNCOMMON IN TYPICAL CHRONIC LYMPHOCYTIC LEUKEMIAS [J].
CRIEL, A ;
WLODARSKA, I ;
MEEUS, P ;
STUL, M ;
LOUWAGIE, A ;
VANHOOF, A ;
HIDAJAT, M ;
MECUCCI, C ;
VANDENBERGHE, H .
BRITISH JOURNAL OF HAEMATOLOGY, 1994, 87 (03) :523-528
[2]  
DOHNER H, 1995, BLOOD, V86, pA345
[3]  
ESCUDIER SM, 1993, BLOOD, V81, P2702
[4]  
Fegan C, 1995, LEUKEMIA, V9, P2003
[5]   CHROMOSOME-ABNORMALITIES INVOLVING BAND 13Q14 IN HEMATOLOGIC MALIGNANCIES [J].
FITCHETT, M ;
GRIFFITHS, MJ ;
OSCIER, DG ;
JOHNSON, S ;
SEABRIGHT, M .
CANCER GENETICS AND CYTOGENETICS, 1987, 24 (01) :143-150
[6]  
*FRENCH COOP GROUP, 1990, BLOOD, V75, P1414
[7]   TRISOMY-12 IN B-CELL CHRONIC LYMPHOCYTIC-LEUKEMIA - ASSESSMENT OF LINEAGE RESTRICTION BY SIMULTANEOUS ANALYSIS OF IMMUNOPHENOTYPE AND GENOTYPE IN INTERPHASE CELLS BY FLUORESCENCE IN-SITU HYBRIDIZATION [J].
GARCIAMARCO, J ;
MATUTES, E ;
MORILLA, R ;
ELLIS, J ;
OSCIER, D ;
FANTES, J ;
CATOVSKY, D ;
PRICE, CM .
BRITISH JOURNAL OF HAEMATOLOGY, 1994, 87 (01) :44-50
[8]  
GEISLER CH, 1989, EUR J HAEMATOL, V43, P397
[9]   PROGNOSTIC IMPORTANCE OF CYTOGENETIC ABNORMALITIES IN PATIENTS WITH CHRONIC LYMPHOCYTIC-LEUKEMIA [J].
HAN, T ;
OZER, H ;
SADAMORI, N ;
EMRICH, L ;
GOMEZ, GA ;
HENDERSON, ES ;
BLOOM, ML ;
SANDBERG, AA .
NEW ENGLAND JOURNAL OF MEDICINE, 1984, 310 (05) :288-292
[10]  
Hernandez JM, 1995, LEUKEMIA, V9, P2140