Association of family history with cancer recurrence and survival among patients with stage III colon cancer

被引:66
作者
Chan, Jennifer A. [1 ]
Meyerhardt, Jeffrey A. [1 ]
Niedzwiecki, Donna [2 ]
Hollis, Donna [2 ]
Saltz, Leonard B. [3 ]
Mayer, Robert J. [1 ]
Thomas, James [4 ]
Schaefer, Paul [5 ]
Whittom, Renaud [6 ]
Hantel, Alexander [7 ]
Goldberg, Richard M. [8 ]
Warren, Robert S. [9 ]
Bertagnolli, Monica [10 ]
Fuchs, Charles S. [1 ]
机构
[1] Dana Farber Canc Inst, Div Med Oncol, Boston, MA 02115 USA
[2] Duke Univ, Med Ctr, CALGB Stat Ctr, Durham, NC USA
[3] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
[4] Ohio State Univ, Columbus, OH 43210 USA
[5] Toledo Community Hosp Oncol Program, Community Clin Oncol Program, Toledo, OH USA
[6] Hop Sacre Coeur, Montreal, PQ H4J 1C5, Canada
[7] Loyola Univ, Stritch Sch Med, Maywood, IL 60153 USA
[8] Univ N Carolina, Dept Hematol Oncol, Chapel Hill, NC USA
[9] Univ Calif San Francisco, Div Surg Oncol, San Francisco, CA 94143 USA
[10] Brigham & Womens Hosp, Div Surg Oncol, Boston, MA 02115 USA
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2008年 / 299卷 / 21期
关键词
D O I
10.1001/jama.299.21.2515
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context A family history of colorectal cancer in a first- degree relative increases the risk of developing colorectal cancer. However, the influence of family history on cancer recurrence and survival among patients with established disease remains uncertain. Objective To examine the association of family history of colorectal cancer with cancer recurrence and survival of patients with colon cancer. Design, Setting, and Participants Prospective observational study of 1087 patients with stage III colon cancer enrolled in a randomized adjuvant chemotherapy trial ( CALGB 89803) between April 1999 and May 2001. Patients provided data on family history at baseline and were followed up until March 2007 for disease recurrence and death ( median follow- up, 5.6 years). In a subset of patients, we assessed microsatellite instability ( MSI) and expression of the mismatch repair ( MMR) proteins MLH1 and MSH2 in tumor specimens. Main Outcome Measures Disease- free survival, recurrence- free survival, and overall survival according to the presence or absence of a family history of colorectal cancer. Results Among 1087 eligible patients, 195 ( 17.9%) reported a family history of colorectal cancer in a first- degree relative. Cancer recurrence or death occurred in 57 of 195 patients ( 29%; 95% confidence interval [ CI], 23%- 36%) with a family history of colorectal cancer and 343 of 892 patients ( 38%; 95% CI, 35%- 42%) without a family history. Compared with patients without a family history, the adjusted hazard ratios ( HRs) among those with 1 or more affected first- degree relatives were 0.72 ( 95% CI, 0.54- 0.96) for disease- free survival, 0.74 ( 95% CI, 0.55- 0.99) for recurrence- free survival, and 0.75 ( 95% CI, 0.54- 1.05) for overall survival. This reduction in risk of cancer recurrence or death associated with a family history became stronger with an increasing number of affected first- degree relatives. Compared with participants without a family history of colorectal cancer, those with 1 affected relative had a multivariate HR of 0.77 ( 95% CI, 0.57- 1.04) for disease- free survival. For participants with 2 or more affected relatives, we observed a greater reduction in risk ( multivariate HR for disease- free survival, 0.49; 95% CI, 0.23- 1.04; P for trend with increasing number of affected relatives=. 01). The improved disease- free survival associated with a family history was independent of tumoral MSI or MMR status. Conclusion Among patients with stage III colon cancer receiving adjuvant chemotherapy, a family history of colorectal cancer is associated with a significant reduction in cancer recurrence and death.
引用
收藏
页码:2515 / 2523
页数:9
相关论文
共 29 条
[1]   Microsatellite instability and colorectal cancer prognosis [J].
Benatti, P ;
Gafà, R ;
Barana, D ;
Marino, M ;
Scarselli, A ;
Pedroni, M ;
Maestri, I ;
Guerzoni, L ;
Roncucci, L ;
Menigatti, M ;
Roncari, B ;
Maffei, S ;
Rossi, G ;
Ponti, G ;
Santini, A ;
Losi, L ;
Di Gregorio, C ;
Oliani, C ;
de Leon, MP ;
Lanza, G .
CLINICAL CANCER RESEARCH, 2005, 11 (23) :8332-8340
[2]  
BERTAGNOLLI MM, 2006, J CLIN ONCOL, P24
[3]  
CANNONALBRIGHT LA, 1989, CANCER, V64, P1971, DOI 10.1002/1097-0142(19891101)64:9<1971::AID-CNCR2820640935>3.0.CO
[4]  
2-L
[5]   COMMON INHERITANCE OF SUSCEPTIBILITY TO COLONIC ADENOMATOUS POLYPS AND ASSOCIATED COLORECTAL CANCERS [J].
CANNONALBRIGHT, LA ;
SKOLNICK, MH ;
BISHOP, T ;
LEE, RG ;
BURT, RW .
NEW ENGLAND JOURNAL OF MEDICINE, 1988, 319 (09) :533-537
[6]   Quantification of the completeness of follow-up [J].
Clark, TG ;
Altman, DG ;
De Stavola, BL .
LANCET, 2002, 359 (9314) :1309-1310
[7]   A PROSPECTIVE-STUDY OF FAMILY HISTORY AND THE RISK OF COLORECTAL-CANCER [J].
FUCHS, CS ;
GIOVANNUCCI, EL ;
COLDITZ, GA ;
HUNTER, DJ ;
SPEIZER, FE ;
WILLETT, WC .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 331 (25) :1669-1674
[8]   Tumor microsatellite instability and clinical outcome in young patients with colorectal cancer [J].
Gryfe, R ;
Kim, H ;
Hsieh, ETK ;
Aronson, MD ;
Holowaty, EJ ;
Bull, SB ;
Redston, M ;
Gallinger, S .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 342 (02) :69-77
[9]  
Johns LE, 2001, AM J GASTROENTEROL, V96, P2992, DOI 10.1111/j.1572-0241.2001.04677.x
[10]   A GENERAL-CLASS OF NONPARAMETRIC-TESTS FOR SURVIVAL ANALYSIS [J].
JONES, MP ;
CROWLEY, J .
BIOMETRICS, 1989, 45 (01) :157-170