Concordance of survival in family members with prostate cancer

被引:53
作者
Hemminki, Kari [1 ]
Ji, Jianguang
Foersti, Asta
Sundquist, Jan
Lenner, Per
机构
[1] German Canc Res Ctr, Div Mol Genet Epidemiol, D-69120 Heidelberg, Germany
关键词
D O I
10.1200/JCO.2007.13.3355
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Several earlier studies have assessed survival in prostate cancer based on familial risk of this disease. As a novel concept, we posit that factors governing survival in prostate cancer are likely to be different from those governing risk of prostate cancer. To prove this, we searched for familial clustering of survival (ie, concordance of survival among family members). Patients and Methods We used the nationwide Swedish Family-Cancer Database to estimate hazard rates (HRs) for cause-specific and overall survival in invasive prostate cancer. HRs show the probability of death in the study group compared with the reference group. The study covered 610 sons of affected fathers with median follow-up times for survival ranging from 34 to 76 months. Results When the survival in sons was analyzed according to the fathers' length of survival, there was a concordance of prognosis; the HR was 0.62 for sons whose fathers had survived longer than 59 months, compared with sons whose fathers had survived fewer than 24 months (P for trend,.02). On a continuous scale, the sons' survival increased almost linearly with the fathers' survival time. When the analysis was reversed and HRs were derived for fathers, the concordance of good and poor survival remained. Conclusion The results are consistent in showing that both good and poor survival in prostate cancer aggregate in families. Genetic factors are likely to contribute to the results, which provide the first challenging population-level evidence on heritability in prognosis of prostate cancer.
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页码:1705 / 1709
页数:5
相关论文
共 30 条
[1]   Significance of familial history of prostate cancer to traditional prognostic variables, genetic biomarkers, and recurrence after radical prostatectomy [J].
Bauer, JJ ;
Srivastava, S ;
Connelly, RR ;
Sesterhenn, IA ;
Preston, DM ;
McLeod, DG ;
Moul, JW .
UROLOGY, 1998, 51 (06) :970-976
[2]   Familial risk of cancer shortly after diagnosis of the first familial tumor [J].
Bermejo, JL ;
Hemminki, K .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2005, 97 (21) :1575-1579
[3]   Role of diet in prostate cancer development and progression [J].
Chan, JM ;
Gann, PH ;
Giovannucci, EL .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (32) :8152-8160
[4]   Annual report to the Nation on the status of cancer, 1975-2002, featuring population-based trends in cancer treatment [J].
Edwards, BK ;
Brown, ML ;
Wingo, PA ;
Howe, HL ;
Ward, E ;
Ries, LAG ;
Schrag, D ;
Jamison, PM ;
Jemal, A ;
Wu, XC ;
Friedman, C ;
Harlan, L ;
Warren, J ;
Anderson, RN ;
Pickle, LW .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2005, 97 (19) :1407-1427
[5]   The role of tumor metastasis suppressors in cancers of breast and prostate [J].
Furuta, Eiji ;
Bandyopadhyay, Sucharita ;
Iiizumi, Megumi ;
Mohinta, Sonia ;
Zhan, Rui ;
Watabe, Kounosuke .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2006, 11 :2845-2860
[6]   DOSE-RESPONSE AND TREND ANALYSIS IN EPIDEMIOLOGY - ALTERNATIVES TO CATEGORICAL ANALYSIS [J].
GREENLAND, S .
EPIDEMIOLOGY, 1995, 6 (04) :356-365
[7]  
Grönberg H, 1998, BRIT J UROL, V82, P564
[8]   Prostate cancer epidemiology [J].
Grönberg, H .
LANCET, 2003, 361 (9360) :859-864
[9]   Mechanisms of disease: Rules for making human tumor cells. [J].
Hahn, WC ;
Weinberg, RA .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 347 (20) :1593-1603
[10]   Is breast cancer prognosis inherited? [J].
Hartman, Mikael ;
Lindstom, Linda ;
Dickman, Paul W. ;
Adami, Hans-Olov ;
Hall, Per ;
Czene, Kamila .
BREAST CANCER RESEARCH, 2007, 9 (03)