Risk of second primary cancers in women diagnosed with endometrial cancer in German and Swedish cancer registries

Along with the increasing incidence and favorable prognosis, more women diagnosed with endometrial cancer may develop second primary cancers (SPCs). We aimed at investigating risk of SPCs after endometrial cancer in Germany and Sweden to provide insight into prevention strategies for SPCs. Endometrial cancer patients diagnosed at age ≥15 years in Germany during 1997–2011 and in Sweden nationwide during 1997–2012 were selected. Standardized incidence ratios (SIRs), calculated as the ratio of observed to expected numbers of cases, were used to assess the risk of a specific second cancer after endometrial cancer for both German and Swedish datasets. Among 46,929 endometrial cancer survivors in Germany and 18,646 in Sweden, overall 2,897 and 1,706 SPCs were recorded, respectively. Significantly elevated SIRs were observed in Germany for ovarian (SIR = 1.3; 95%CI:1.1–1.5) and kidney cancers [1.6 (1.3–1.8)], while in Sweden the SIRs were 5.4 (4.6–6.3) and1.4 (1.0–1.9), respectively. Elevated risk for second ovarian endometrioid carcinoma was pronounced after early (<55 years) onset endometrial cancer in Germany [9.0 (4.8–15)] and Sweden [7.7 (5.1–11)]. In Germany elevated risks were found for second ovarian endometrioid carcinoma after endometrioid histology of first endometrial cancer [6.3 (4.0–9.4)] and for second kidney cancer after clear cell histology of endometrial cancer [4.9 (1.6–11)]. We found exceptionally elevated risk of second ovarian endometrioid carcinoma after endometrial cancer of the same histology or of early onset. Risk for second kidney cancer was also increased, particularly after endometrial cancer of clear cell histology. Cancer prevention strategies should focus on these cancers after endometrial cancer diagnosis.

[1]  M. Plummer,et al.  International agency for research on cancer. , 2020, Archives of pathology.

[2]  H. Brenner,et al.  Distribution and risk of the second discordant primary cancers combined after a specific first primary cancer in German and Swedish cancer registries. , 2015, Cancer letters.

[3]  H. Brenner,et al.  Recent cancer survival in Germany: An analysis of common and less common cancers , 2015, International journal of cancer.

[4]  C. Mathers,et al.  Cancer incidence and mortality worldwide: Sources, methods and major patterns in GLOBOCAN 2012 , 2015, International journal of cancer.

[5]  K. Hemminki,et al.  Effect of a detailed family history of melanoma on risk for other tumors: a cohort study based on the nationwide Swedish Family-Cancer Database. , 2014, The Journal of investigative dermatology.

[6]  J. Chang-Claude,et al.  Hormonal, metabolic, and inflammatory profiles and endometrial cancer risk within the EPIC cohort--a factor analysis. , 2013, American journal of epidemiology.

[7]  J. Ferlay,et al.  Cancer incidence and mortality patterns in Europe: estimates for 40 countries in 2012. , 2013, European journal of cancer.

[8]  H. Hinshaw,et al.  The Risk of Subsequent Malignancies in Women With Uterine Papillary Serous or Clear Cell Endometrial Cancers , 2013, International Journal of Gynecologic Cancer.

[9]  H. Brenner,et al.  Survival of endometrial cancer patients in Germany in the early 21st century: a period analysis by age, histology, and stage , 2012, BMC Cancer.

[10]  H. Brenner,et al.  Survival from common and rare cancers in Germany in the early 21st century. , 2012, Annals of oncology : official journal of the European Society for Medical Oncology.

[11]  Randall W Burt,et al.  A population-based study of subsequent primary malignancies after endometrial cancer: genetic, environmental, and treatment-related associations. , 2010, International journal of radiation oncology, biology, physics.

[12]  J. Kwon,et al.  Secondary Cancer Prevention During Follow-up for Endometrial Cancer , 2009, Obstetrics and gynecology.

[13]  C. Holschneider,et al.  Coexisting Ovarian Malignancy in Young Women With Endometrial Cancer , 2005, Obstetrics and gynecology.

[14]  K. Hemminki,et al.  Familial association of specific histologic types of ovarian malignancy with other malignancies , 2004, Cancer.

[15]  L. Aaltonen,et al.  Subsequent primary malignancies after endometrial carcinoma and ovarian carcinoma , 2003, Cancer.

[16]  R. Kaaks,et al.  Obesity , Endogenous Hormones , and Endometrial Cancer Risk : A Synthetic Review 1 , 2002 .

[17]  K. Hemminki,et al.  Endometrial cancer in the family-cancer database. , 1999, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

[18]  K. Hemminki,et al.  Multiple primary cancers as clues to environmental and heritable causes of cancer and mechanisms of carcinogenesis. , 2004, IARC scientific publications.

[19]  K. Hemminki,et al.  The nation-wide Swedish family-cancer database--updated structure and familial rates. , 2001, Acta oncologica.