Multiple primary cancers among colorectal cancer survivors in Queensland, Australia, 1996-2007

被引:9
|
作者
Dasgupta, Paramita [1 ]
Youlden, Danny R. [1 ]
Baade, Peter D. [1 ,2 ,3 ]
机构
[1] Canc Council Queensland, Viertel Ctr Res Canc Control, Brisbane, Qld 4001, Australia
[2] Queensland Univ Technol, Sch Publ Hlth, Brisbane, Qld 4001, Australia
[3] Griffith Univ, Griffith Hlth Inst, Gold Coast, Australia
基金
英国医学研究理事会; 澳大利亚国家健康与医学研究理事会;
关键词
Colon cancer; Rectal cancer; Multiple primary cancers; Risk factors; SUBSEQUENT PRIMARY CANCERS; 2ND PRIMARY CANCERS; BREAST-CANCER; RISK-FACTORS; RADIOTHERAPY; DIAGNOSIS; PROSTATE; OUTCOMES; COLON;
D O I
10.1007/s10552-012-9990-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To quantify the demographic and clinical factors associated with an increased risk of multiple primary cancers (MPCs) among colorectal cancer survivors. Standardized incidence ratios for MPCs were calculated for residents of Queensland, Australia, who were diagnosed with a first primary colorectal cancer between 1996 and 2005 and survived for at least 2 months. Relative risk ratios were calculated for all MPCs combined and selected individual sites using multivariate Poisson models. A total of 1,615 MPCs were observed among 15,755 study patients. The cohort had a significant excess risk of developing subsequent colorectal (SIR = 1.47, 95 % CI 1.30-1.66) or non-colorectal (SIR = 1.24, 95 % CI 1.18-1.31) cancers relative to the incidence of cancer in the general population. Age at initial diagnosis, follow-up time, initial colorectal subsite, and surgical treatment were independently associated (p < 0.01) with the overall risk of developing MPCs after adjustment. The relative risk ratio was 1.23 (95 % CI 1.07-1.41) for those aged 20-59 years compared with the 70-79 age group and 0.82 (95 % CI 0.72-0.92) for 1-5-year follow-up relative to the first year. The likelihood of being diagnosed with a MPC was 33 % higher (95 % CI 1.12-1.56) for surgically treated patients and 45 % higher (95 % CI 1.29-1.64) after proximal colon cancers relative to rectal cancer. While these population-based results do not incorporate all possible risk factors, they form an important foundation from which to further investigate the etiological causes that result in the development of MPCs among colorectal cancer survivors.
引用
收藏
页码:1387 / 1398
页数:12
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