Tumor karyotype predicts clinical outcome in colorectal cancer patients

被引:47
作者
Bardi, G
Fenger, C
Johansson, B
Mitelman, F
Heim, S
机构
[1] St Savas Oncol Hosp Athens, G Papanikolaou Res Ctr, Dept Genet, Athens 11522, Greece
[2] Odense Univ Hosp, Dept Pathol, DK-5000 Odense, Denmark
[3] Univ Lund Hosp, Dept Clin Genet, S-22185 Lund, Sweden
[4] Norwegian Radium Hosp, Dept Canc Genet, Oslo, Norway
关键词
D O I
10.1200/JCO.2004.11.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose To investigate the prognostic value of the overall karyotypic features and specific chromosome aberrations in colorectal cancer (CRC). Patients and Methods Cytogenetic features of 150 primary CRCs investigated at the time of surgery were correlated with patient survival by univariate and multivariate analyses, using classical clinicopathologic parameters as covariates. Results In univariate analysis, in addition to tumor grade and clinical stage, structural aberrations as well as rearrangements of chromosomes 8 and 16 were significantly correlated with shorter overall survival. Karyotypic complexity, rearrangements of chromosomes 8 and 16, and loss of chromosome 4 were significantly correlated with shorter disease-free survival. In multivariate analysis, in addition to tumor grade, the type of chromosome aberrations (structural or numerical), ploidy, and loss of chromosome 18 came across as independent prognostic factors in the group of all patients. In the subset of patients with stage I and II carcinomas, none of the clinicopathologic variables could independently predict patient survival, whereas the presence of structural chromosomal aberrations was the only independent predictor of poor prognosis. In the subset of patients with stage III carcinomas, the presence of structural changes of chromosome 8 was a stronger independent predictor of prognosis than was tumor grade. Conclusion Cytogenetic tumor features are valuable predictors of prognosis in CRC patients. The tumor karyotype should therefore be taken into account in the clinical management of patients with this disease, especially for patients having cancers of the early or intermediate stages I, II, and III. (C) 2004 by American Society of Clinical Oncology.
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页码:2623 / 2634
页数:12
相关论文
共 34 条
[1]  
Arribas R, 1999, CLIN CANCER RES, V5, P3454
[2]   Cytogenetic comparisons of synchronous carcinomas and polyps in patients with colorectal cancer [J].
Bardi, G ;
Parada, LA ;
Bomme, L ;
Pandis, N ;
Willen, R ;
Johansson, B ;
Jeppsson, B ;
Beroukas, K ;
Heim, S ;
Mitelman, F .
BRITISH JOURNAL OF CANCER, 1997, 76 (06) :765-769
[3]  
BARDI G, 1993, CANCER, V71, P306, DOI 10.1002/1097-0142(19930115)71:2<306::AID-CNCR2820710207>3.0.CO
[4]  
2-C
[5]  
Bardi G, 1997, INT J CANCER, V72, P604, DOI 10.1002/(SICI)1097-0215(19970807)72:4<604::AID-IJC9>3.0.CO
[6]  
2-U
[7]   CYTOGENETIC ANALYSIS OF 52 COLORECTAL CARCINOMAS - NONRANDOM ABERRATION PATTERN AND CORRELATION WITH PATHOLOGICAL PARAMETERS [J].
BARDI, G ;
JOHANSSON, B ;
PANDIS, N ;
MANDAHL, N ;
BAKJENSEN, E ;
LINDSTROM, C ;
TORNQVIST, A ;
FREDERIKSEN, H ;
ANDRENSANDBERG, A ;
MITELMAN, F ;
HEIM, S .
INTERNATIONAL JOURNAL OF CANCER, 1993, 55 (03) :422-428
[8]  
BARDI G, 1993, CANCER RES, V53, P1895
[9]   KARYOTYPIC CHARACTERIZATION OF COLORECTAL ADENOCARCINOMAS [J].
BARDI, G ;
SUKHIKH, T ;
PANDIS, N ;
FENGER, C ;
KRONBORG, O ;
HEIM, S .
GENES CHROMOSOMES & CANCER, 1995, 12 (02) :97-109
[10]   TRISOMY-7 AS THE SOLE CYTOGENETIC ABERRATION IN THE EPITHELIAL COMPONENT OF A COLONIC ADENOMA [J].
BARDI, G ;
PANDIS, N ;
FENGER, C ;
HEIM, S .
CANCER GENETICS AND CYTOGENETICS, 1995, 82 (01) :82-84