Prognostic significance of DNA replication errors in young patients with colorectal cancer

被引:106
作者
Lukish, JR
Muro, K
DeNobile, J
Katz, R
Williams, J
Cruess, DF
Drucker, W
Kirsch, I
Hamilton, SR
机构
[1] Natl Naval Med Ctr, Dept Surg, Bethesda, MD 20814 USA
[2] Natl Naval Med Ctr, Dept Pathol, Bethesda, MD USA
[3] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21218 USA
[4] Johns Hopkins Univ, Sch Med, Ctr Oncol, Baltimore, MD 21218 USA
[5] Uniformed Serv Univ Hlth Sci, Dept Surg, Bethesda, MD 20814 USA
[6] Uniformed Serv Univ Hlth Sci, Dept Biostat, Bethesda, MD 20814 USA
[7] NCI, USN, Med Oncol Branch, Bethesda, MD 20892 USA
关键词
D O I
10.1097/00000658-199801000-00008
中图分类号
R61 [外科手术学];
学科分类号
摘要
Objective To determine:he DNA replication error (RER) status in young patients with colorectal cancer (CRC), and to compare the clinical and pathologic characteristics of RER-positive and RER-negative cases. Summary Background Data. Recent studies suggest that patients with RER-positive CRC have an improved prognosis. Further data are required to confirm this observation in young CRC patients. Methods All patients 40 years of age and younger with CRC admitted to the National Naval Medical Center between 1970 and 1992 were considered for inclusion in the study. After review, 36 patients for when? the original archived pathology specimen could be retrieved sewed as the study population. The RER status was determined using a previously described polymerase chain reaction-based assay. The clinical and pathologic features and survival data were compared is RER status. Results RER-positive tumors were found in 17 cases (47%). There was no significant difference in Dukes' stage or histologic grade at the time of diagnosis between patients with PER-positive tumors compared to RER-negative tumors. Patients with PER-positive tumors were found to have an improved prognosis: the 5-year survival probability for patients with RER-positive tumors was 68%, as compared to 32% for patients with RER-negative tumors (p < 0.05). Conclusions RER-positive tumors are common in young patients with CRC, and patients with RER-positive tumors have a significantly improved prognosis. Because of their young age, survival data and prognosis play an important role in the overall treatment plan of young patients with CRC. Therefore, knowledge of RER status could affect initial therapy, postoperative chemotherapy, and follow-up.
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页码:51 / 56
页数:6
相关论文
共 25 条
[1]  
AALTONEN LA, 1994, CANCER RES, V54, P1645
[2]   CLUES TO THE PATHOGENESIS OF FAMILIAL COLORECTAL-CANCER [J].
AALTONEN, LA ;
PELTOMAKI, P ;
LEACH, FS ;
SISTONEN, P ;
PYLKKANEN, L ;
MECKLIN, JP ;
JARVINEN, H ;
POWELL, SM ;
JEN, J ;
HAMILTON, SR ;
PETERSEN, GM ;
KINZLER, KW ;
VOGELSTEIN, B ;
DELACHAPELLE, A .
SCIENCE, 1993, 260 (5109) :812-816
[3]  
Anthoney DA, 1996, CANCER RES, V56, P1374
[4]   A MISMATCH RECOGNITION DEFECT IN COLON-CARCINOMA CONFERS DNA MICROSATELLITE INSTABILITY AND A MUTATOR PHENOTYPE [J].
AQUILINA, G ;
HESS, P ;
BRANCH, P ;
MACGEOCH, C ;
CASCIANO, I ;
KARRAN, P ;
BIGNAMI, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (19) :8905-8909
[5]  
BASS BL, 1993, ADV COLORECTAL CARCI, P52
[6]   MUTATOR PHENOTYPES IN HUMAN COLORECTAL-CARCINOMA CELL-LINES [J].
BHATTACHARYYA, NP ;
SKANDALIS, A ;
GANESH, A ;
GRODEN, J ;
MEUTH, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (14) :6319-6323
[7]   DEFECTIVE MISMATCH BINDING AND A MUTATOR PHENOTYPE IN CELLS TOLERANT TO DNA DAMAGE [J].
BRANCH, P ;
AQUILINA, G ;
BIGNAMI, M ;
KARRAN, P .
NATURE, 1993, 362 (6421) :652-654
[8]   DNA MISMATCH REPAIR AND CANCER [J].
CHUNG, DC ;
RUSTGI, AK .
GASTROENTEROLOGY, 1995, 109 (05) :1685-1699
[9]  
ESHLEMAN JR, 1995, ONCOGENE, V10, P33
[10]   THE MOLECULAR-BASIS OF TURCOTS-SYNDROME [J].
HAMILTON, SR ;
LIU, B ;
PARSONS, RE ;
PAPADOPOULOS, N ;
JEN, J ;
POWELL, SM ;
KRUSH, AJ ;
BERK, T ;
COHEN, Z ;
TETU, B ;
BURGER, PC ;
WOOD, PA ;
TAQI, F ;
BOOKER, SV ;
PETERSEN, GM ;
OFFERHAUS, GJA ;
TERSMETTE, AC ;
GIARDIELLO, FM ;
VOGELSTEIN, B ;
KINZLER, KW .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 332 (13) :839-847