Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2012 Jun;19(6):1887-96.
doi: 10.1245/s10434-011-2193-2. Epub 2012 Jan 7.

Risk of subsequent primary thyroid cancer after another malignancy: latency trends in a population-based study

Affiliations

Risk of subsequent primary thyroid cancer after another malignancy: latency trends in a population-based study

Geeta Lal et al. Ann Surg Oncol. 2012 Jun.

Abstract

Purpose: To evaluate the risk of a subsequent primary thyroid cancer (SPTC) in patients with common invasive cancers, with attention to latency trends and histology associations.

Methods: Patients with one of 10 common invasive cancers were followed from 1975 to 2008 in 9 registries participating in the National Cancer Institute's Surveillance, Epidemiology, and End Results (SEER) database. Standardized incidence ratios (SIRs) for SPTC were determined by the multiple primary-SIR program in SEER*Stat.

Results: A total of 2502 SPTCs were observed. Greatly elevated SIRs for SPTC were noted for 9 of 10 evaluated cancers in the 12 months after initial diagnosis. The SIRs remained elevated 12-59 months after diagnosis for all cancers except leukemia, uterine, and bladder cancers. Increased risks persisted 60-119 months beyond diagnosis for renal (SIR 2.56) and breast cancer (SIR 1.16); and 120+ months for renal cancer (SIR 2.46). Increased SPTC risk after renal and female breast cancers was mostly seen in nonirradiated patients. The principal histology association was between papillary thyroid cancer and renal cell carcinomas.

Conclusions: Many common cancers are associated with increased risk of SPTC beyond 12 months of initial diagnosis. Although this can be explained partly by continued surveillance bias, radiation effects, and known rare familial associations for some tumors, these factors alone are unlikely to explain the persistent, significant two-way association with renal and breast cancers. Additional research is needed to further define the biological and environmental mechanisms underlying these associations.

PubMed Disclaimer

Figures

FIG. 1
FIG. 1
a Latency course of risk of SPTC for tumors associated with persistently elevated SIRs >1 beyond 60 months of diagnosis of the initial primary. The error bars indicate the 95% CIs. b Latency course of risk of SPTC for tumors associated with delayed elevated SIRs of >1 beyond 60 months of diagnosis of the initial primary. The error bars indicate the 95% CIs. Note that the SIRs cross 1 after 59 months of diagnosis, then show a later increase beyond 120 months of diagnosis of the initial primary tumor

Similar articles

Cited by

References

    1. Howlader N, Krapcho M, Neyman N, et al., editors. SEER cancer statistics review, 1975–2008. Bethesda, MD: National Cancer Institute; 2010. http://seer.cancer.gov/csr/1975_2008/
    1. Brown P, Chen J, Hitchcock YJ, Szabo A, Shrieve DC, Tward JD. The risk of second primary malignancies up to three decades after the treatment of differentiated thyroid cancer. J Clin Endocrinol Metab. 2008;93:504–15. - PubMed
    1. Canchola AJ, Horn-Ross PL, Purdie DM. Risk of second primary malignancies in women with papillary thyroid cancer. Am J Epidemiol. 2006;163:521–7. - PubMed
    1. Rubino C, de Vathaire F, Dottorini ME, et al. Second primary malignancies in thyroid cancer patients. Br J Cancer. 2003;89:1638–44. - PMC - PubMed
    1. Berthe E, Henry-Amar M, Michels JJ, et al. Risk of second primary cancer following differentiated thyroid cancer. Eur J Nucl Med Mol Imaging. 2004;31:685–91. - PubMed

MeSH terms