Risk of second cancer among women with breast cancer

被引:186
|
作者
Mellemkjær, L
Friis, S
Olsen, JH
Scélo, G
Hemminki, K
Tracey, E
Andersen, A
Brewster, DH
Pukkala, E
McBride, ML
Kliewer, EV
Tonita, JM
Kee-Seng, C
Pompe-Kirn, V
Martos, C
Jonasson, JG
Boffetta, P
Brennan, P
机构
[1] Danish Canc Soc, Inst Canc Epidemiol, DK-2100 Copenhagen, Denmark
[2] IARC, GeneEnvironm Epidemiol Grp, Lyon, France
[3] German Canc Res Ctr, Div Mol Genet Epidemiol, D-6900 Heidelberg, Germany
[4] Karolinska Inst, Dept Biosci, Novum, Huddinge, Sweden
[5] New S Wales Canc Registry, Eveleigh, NSW, Australia
[6] Inst Populat Based Canc Res, Oslo, Norway
[7] Scottish Canc Registry Informat Serv, NHS Natl Serv Scotland, Edinburgh, Midlothian, Scotland
[8] Finnish Canc Registry, Inst Stat & Epidemiol Canc Res, FIN-00170 Helsinki, Finland
[9] British Columbia Canc Agcy, Canc Control Res Programme, Vancouver, BC V5Z 4E6, Canada
[10] CancerCare Manitoba, Epidemiol & Canc Registry, Winnipeg, MB, Canada
[11] Univ Manitoba, Winnipeg, MB, Canada
[12] Saskatchewan Canc Agcy, Program Evaluat & Surveillan, Regina, SK, Canada
[13] Ctr Mol Epidemiol, Singapore, Singapore
[14] Canc Registry Slovenia, Inst Oncol, Ljubljana, Slovenia
[15] Canc Registry Zaragoza, Hlth Dept Aragon Govt, Zaragoza, Spain
[16] Iceland Canc Soc, Iceland Canc Registry, Reykjavik, Iceland
[17] Univ Iceland, Fac Med, Reykjavik, Iceland
关键词
female breast cancer; second primary cancer; multi-centre cohort study;
D O I
10.1002/ijc.21651
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A large number of women survive a diagnosis of breast cancer. Knowledge of their risk of developing a new primary cancer is important not only in relation to potential side effects of their cancer treatment, but also in relation to the possibility of shared etiology with other types of cancer. A cohort of 525,527 women with primary breast cancer was identified from 13 population-based cancer registries in Europe, Canada, Australia and Singapore, and followed for second primary cancers within the period 1943-2000. We used cancer incidence rates of first primary cancer for the calculation of standardized incidence ratios (SIRs) of second primary cancer. Risk of second primary breast cancer after various types of nonbreast cancer was also computed. For all second cancer sites combined, except contralateral breast cancer, we found a SIR of 1.25 (95% CI = 1.24-1.26) on the basis of 31,399 observed cases after first primary breast cancer. The overall risk increased with increasing time since breast cancer diagnosis and decreased by increasing age at breast cancer diagnosis. There were significant excesses of many different cancer sites; among these the excess was larger than 150 cases for stomach (SIR = 1.35), colorectal (SIR = 1.22), lung (SIR = 1.24), soft tissue sarcoma (SIR = 2.25), melanoma (SIR = 1.29), non-melanoma skin (SIR = 1.58), endometrium (SIR = 1.52), ovary (SIR = 1.48), kidney (SIR = 1.27), thyroid gland (SIR = 1.62) and leukaemia (SIR = 1.52). The excess of cancer after a breast cancer diagnosis is likely to be explained by treatment for breast cancer and by shared genetic or environmental risk factors, although the general excess of cancer suggests that there may be additional explanations such as increased surveillance and general cancer susceptibility. (c) 2005 Wiley-Liss, Inc.
引用
收藏
页码:2285 / 2292
页数:8
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