KI-RAS MUTATIONS AS A PROGNOSTIC FACTOR IN EXTRAHEPATIC BILE SYSTEM CANCER

被引:47
作者
MALATS, N
PORTA, M
PINOL, JL
COROMINAS, JM
RIFA, J
REAL, FX
机构
[1] UNIV AUTONOMA BARCELONA,INST MUNICIPAL INVEST MED,DEPT EPIDEMIOL,E-08003 BARCELONA,SPAIN
[2] UNIV AUTONOMA BARCELONA,INST MUNICIPAL INVEST MED,DEPT IMMUNOL,E-08003 BARCELONA,SPAIN
[3] HOSP MARE DEU ESPERANCA,BARCELONA,SPAIN
[4] HOSP SON DURETA,PALMA DE MALLORCA,SPAIN
关键词
D O I
10.1200/JCO.1995.13.7.1679
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To assess the prevalence and prognostic significance of Ki-ras codon 12 mutations in extrahepatic biliary system cancer (EBSC). Patients and Methods: Patients diagnosed with EBSC between 1980 and 1990 (N = 111) were selected from two hospitals. DNA was amplified from paraffin-embedded tissues and mutations in codon 12 of Ki-ras were detected using the artificial restriction fragment-length polymorphism (RFLP) technique. Results: Tissue was available from 68.5% of patients, The prevalence of mutations was 41%, There wets no association between mutations and clinical and pathologic characteristics; however, mutations in Ki-ros were associated with survival, with a median survival duration of 7.7 months for patients with wild-type Ki-ras and 1.7 months for patients with mutated tumors (hazards ratio [HR] = 1.67; P = .075), Among patients with stage I to II tumors, the chance of dying of patients with the mutation was 7.8 times higher than that of patients without the mutation (P = .087); the corresponding HR for patients with stage III to IV disease was 2.9 (P = .003), After adjusting for age, tumor site, histology, differentiation, and stage, the HR for Ki-ras mutations was 2.12 (P = .026). Conclusion: Ki-ras codon 12 mutations are an independent prognostic indicator in patients with EBSC, Mutation detection may be of help in the management of these patients. (C) 1995 by American Society of Clinical Oncology.
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页码:1679 / 1686
页数:8
相关论文
共 46 条
[1]   BILIARY CARCINOMA - A REVIEW OF 109 CASES [J].
ALEXANDER, F ;
ROSSI, RL ;
OBRYAN, M ;
KHETTRY, U ;
BRAASCH, JW ;
WATKINS, E .
AMERICAN JOURNAL OF SURGERY, 1984, 147 (04) :503-509
[2]   ASSOCIATION OF P53 PROTEIN EXPRESSION WITH TUMOR-CELL PROLIFERATION RATE AND CLINICAL OUTCOME IN NODE-NEGATIVE BREAST-CANCER [J].
ALLRED, DC ;
CLARK, GM ;
ELLEDGE, R ;
FUQUA, SAW ;
BROWN, RW ;
CHAMNESS, GC ;
OSBORNE, CK ;
MCGUIRE, WL .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1993, 85 (03) :200-206
[3]   MOST HUMAN CARCINOMAS OF THE EXOCRINE PANCREAS CONTAIN MUTANT C-K-RAS GENES [J].
ALMOGUERA, C ;
SHIBATA, D ;
FORRESTER, K ;
MARTIN, J ;
ARNHEIM, N ;
PERUCHO, M .
CELL, 1988, 53 (04) :549-554
[4]  
ARMITAGE P, 1987, STATISTICAL METHODS
[5]   COMPARATIVE-ANALYSIS OF MUTATIONS IN THE P53 AND K-RAS GENES IN PANCREATIC-CANCER [J].
BERROZPE, G ;
SCHAEFFER, J ;
PEINADO, MA ;
REAL, FX ;
PERUCHO, M .
INTERNATIONAL JOURNAL OF CANCER, 1994, 58 (02) :185-191
[6]  
BOS JL, 1989, CANCER RES, V49, P4682
[7]   FREQUENCY AND SPECTRUM OF MUTATIONS AT CODON-12 AND CONDON-13 OF THE C-K-RAS GENE IN HUMAN TUMORS [J].
CAPELLA, G ;
CRONAUERMITRA, S ;
PEINADO, MA ;
PERUCHO, M .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1991, 93 :125-131
[8]  
COX DR, 1972, J R STAT SOC B, V34, P187
[9]   ACCUMULATION OF NUCLEAR P53 AND TUMOR PROGRESSION IN BLADDER-CANCER [J].
ESRIG, D ;
ELMAJIAN, D ;
GROSHEN, S ;
FREEMAN, JA ;
STEIN, JP ;
CHEN, SC ;
NICHOLS, PW ;
SKINNER, DG ;
JONES, PA ;
COTE, RJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 331 (19) :1259-1264
[10]  
FALKSON G, 1984, CANCER, V54, P965, DOI 10.1002/1097-0142(19840915)54:6<965::AID-CNCR2820540603>3.0.CO