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
Review
. 2010 Oct;5(10 Suppl 4):S260-5.
doi: 10.1097/JTO.0b013e3181f1f62d.

Epidemiology of thymoma and associated malignancies

Affiliations
Review

Epidemiology of thymoma and associated malignancies

Eric A Engels. J Thorac Oncol. 2010 Oct.

Abstract

Background: Thymoma is a rare malignancy of unknown etiology.

Methods: The author examined patterns in thymoma incidence in the US general population using data from Surveillance, Epidemiology, and End Results (SEER) cancer registries. Prior studies concerning the risk of additional malignancies in thymoma patients were reviewed.

Results: Based on cancer registry data, the overall incidence of thymoma in the US is 0.13 per 100,000 person-years. Thymoma is exceedingly uncommon in children and young adults, rises in incidence in middle age, and peaks in the seventh decade of life. Thymoma incidence is especially high among Asians and Pacific Islanders in the US. While several studies based at single treatment centers have suggested that thymoma patients have a broadly increased risk for other malignancies, follow up data from US cancer registries support a more limited spectrum of cancer risk. In particular, thymoma patients have a subsequently elevated risk for developing B-cell non-Hodgkin's lymphoma. Based on limited data, thymoma patients may also have an elevated risk for developing soft tissue sarcomas.

Discussion: Thymoma is a rare malignancy. The excess risk for non-Hodgkin's lymphoma is consistent with an effect of immune disturbance arising from the thymoma or its treatment. While descriptive epidemiologic data may yield clues to the etiology of thymoma, large multi-center case-control studies will be required to formally evaluate environmental and genetic risk factors.

PubMed Disclaimer

Figures

Figure 1
Figure 1. Thymoma incidence in the U.S, according to calendar year and age at diagnosis
Panel A shows incidence as a function of calendar year of diagnosis. Incidence is per 100,000 person-years and is standardized to the 2000 U.S. general population. Panel B shows incidence as a function of age of diagnosis. Crude incidence is per 100,000 person-years. Data are from the SEER9 cancer registries (1973-2006, www.seer.cancer.gov).
Figure 1
Figure 1. Thymoma incidence in the U.S, according to calendar year and age at diagnosis
Panel A shows incidence as a function of calendar year of diagnosis. Incidence is per 100,000 person-years and is standardized to the 2000 U.S. general population. Panel B shows incidence as a function of age of diagnosis. Crude incidence is per 100,000 person-years. Data are from the SEER9 cancer registries (1973-2006, www.seer.cancer.gov).

References

    1. Müller-Hermelink HK, Marx A. Thymoma. Current Opin Oncol. 2000;12:426–33. - PubMed
    1. Buckley C, Douek D, Newsom-Davis J, Vincent A, Wilcox N. Mature, long-lived CD4+ and CD8+ T cells are generated by the thymoma in myasthenia gravis. Ann Neurol. 2001;50:64–72. - PubMed
    1. Souadjian JV, Enriquez P, Silverstein MN, Pépin J-M. The spectrum of diseases associated with thymoma. Arch Intern Med. 1974;134:374–79. - PubMed
    1. Engels EA, Pfeiffer RM. Malignant thymoma in the United States: demographic patterns in incidence and associations with subsequent malignancies. Int J Cancer. 2003;105:546–51. - PubMed
    1. Thomas CR, Wright CD, Loehrer PJ., Sr. Thymoma: state of the art. J Clin Oncol. 1999;17:2280–2289. - PubMed

MeSH terms