Second Primary Cancers After Gastric Cancer, and Gastric Cancer as Second Primary Cancer

被引:9
|
作者
Zheng, Guoqiao [1 ,2 ,3 ]
Sundquist, Kristina [3 ,4 ,5 ]
Sundquist, Jan [3 ,4 ,5 ,6 ]
Chen, Tianhui [7 ]
Foersti, Asta [1 ,3 ,8 ,9 ]
Hemminki, Akseli [10 ,11 ]
Hemminki, Kari [1 ,2 ,3 ,12 ,13 ]
机构
[1] German Canc Res Ctr, Div Mol Genet Epidemiol, Heidelberg, Germany
[2] German Canc Res Ctr, Div Canc Epidemiol, Heidelberg, Germany
[3] Lund Univ, Ctr Primary Hlth Care Res, Malmo, Sweden
[4] Icahn Sch Med Mt Sinai, Dept Family Med & Community Hlth, New York, NY 10029 USA
[5] Icahn Sch Med Mt Sinai, Dept Populat Hlth Sci & Policy, New York, NY 10029 USA
[6] Shimane Univ, Ctr Community Based Healthcare Res & Educ CoHRE, Sch Med, Dept Funct Pathol, Matsue, Shimane, Japan
[7] Chinese Acad Sci, Univ Chinese Acad Sci, Zhejiang Canc Hosp, Canc Hosp,Inst Basic Med & Canc,Dept Canc Prevent, Hangzhou 310022, Peoples R China
[8] Hopp Childrens Canc Ctr KiTZ, Heidelberg, Germany
[9] German Canc Consortium DKTK, German Canc Res Ctr DKFZ, Div Pediat Neurooncol, Heidelberg, Germany
[10] Univ Helsinki, Translat Immunol Res Program, Canc Gene Therapy Grp, Helsinki, Finland
[11] Helsinki Univ Hosp, Comprehens Canc Ctr, Helsinki, Finland
[12] Charles Univ Prague, Fac Med, Biomed Ctr, Plzen 30605, Czech Republic
[13] Charles Univ Prague, Biomed Ctr Pilsen, Plzen 30605, Czech Republic
来源
CLINICAL EPIDEMIOLOGY | 2021年 / 13卷
基金
欧盟地平线“2020”; 瑞典研究理事会;
关键词
cancer incidence; relative risk; second primary cancer; cancer etiology; stomach cancer; RENAL-TRANSPLANTATION; UNITED-STATES; RISK; MORTALITY; MALIGNANCY; GENETICS; MUTATION; TRENDS;
D O I
10.2147/CLEP.S304332
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background: Second primary cancers (SPCs) are increasing, which may negatively influ-ence patient survival. Gastric cancer (GC) has poor survival and when it is diagnosed as SPC it is often the cause of death. We wanted to analyze the risk of SPCs after GC and the risk of GC as SPC after any cancer. Such bidirectional analysis is important in relation to fatal cancers because SPCs may be under-reported in the short-term survival period. Methods: Cancers were obtained from the Swedish Cancer Registry from years 1990 through 2015. Standardized incidence ratios (SIRs) were used to estimate bidirectional relative. Results: We identified 23,137 GC patients who developed 1042 SPCs (4.5%); 2158 patients had GC as SPC. While the risk for three SPCs was increased after GC, seven first primary cancers were followed by an increased risk of GC as SPC, including esophageal, colorectal, bladder, squamous cell skin and breast cancers and non-Hodgkin lymphoma. Breast cancer, which was followed by a diagnosis of second GC, showed an excess of lobular histology. Conclusion: Multiple primary cancers in the same individuals may signal genetic predis-position. Accordingly, the association of GC with breast cancer may be related to mutations in the CDH1 gene, and clustering of colorectal, small intestinal and bladder cancers could be related to Lynch syndrome. The third line of findings supports a contribution of immune dysfunction on the increased risk of GC as SPC after skin cancer and non-Hodgkin lymphoma. Early detection of GC in the risk groups could save lives.
引用
收藏
页码:515 / 525
页数:11
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