Abstract
Objectives
Thymic carcinoma and thymic neuroendocrine tumor (NET) are rare and are more likely to develop second malignancies. The purpose of this study was to explore the incidence and lifetime risk of second malignancies in thymic carcinoma and thymic NET.
Methods
The standardized incidence ratio (SIR) and the age-adjusted cancer incidence of the thymic carcinoma and thymic NET patients with second malignancies were retrospectively calculated by using the Surveillance, Epidemiology, and End Results (SEER) database. Prognosis results were also determined by Kaplan–Meier analysis and Cox regression.
Results
1130 patients with thymic carcinoma (73 patients had second malignancies) and 263 patients with thymic NET (19 patients had second malignancies) from 2000 to 2018 are included. Patients with thymic carcinoma (SIR: 1.36, 95% CI 1.08–1.69) and with thymic NET (SIR: 1.73, 95% CI 1.13–2.54) demonstrate an increased overall risk of developing second malignancies in various organ systems. The age-adjusted cancer incidence of second malignancies in patients with thymic carcinoma is 3058.48 per 100,000 persons (4178.46 per 100,000 persons in patients with thymic NET). Age at diagnosis is a significant risk factor for the development of second malignancies.
Conclusion
The incidence of second malignancies in patients with thymic carcinoma and thymic NET is significantly higher than the patients in the normal population. The occurrence of second malignancies is not related to the use of different treatments. It is important to extend the follow-up period and add other screening methods.
Similar content being viewed by others
Avoid common mistakes on your manuscript.
Introduction
The incidences of thymic malignancies that are rare tumors are less than 1% among adult cancers (Engels 2010). Thymoma, thymic carcinoma, and thymic neuroendocrine tumor (NET) are classified as thymic epithelial tumors (Venuta et al. 2010). Thymic carcinoma is a very rare malignant tumor, and its prognosis is worse than thymoma (Ahmad et al. 2015). Thymic NET is rarer and accounts for about 2–5% of thymic cancers, and its prognosis is poor (Gaur et al. 2010).
Previous studies have revealed the association between the incidence of second malignant tumors and thymoma (LeGolvan and Abell 1977; Gray and Gutowski 1979; Lewis et al. 1987; Couture and Mountain 1990; Wilkins et al. 1999; Welsh et al. 2000); because thymic carcinoma and thymic NET are rare, there are few studies on second malignancies arising after diagnosis. Badve suggested that 14 of 85 patients had a second malignancy including embryonal carcinoma, prostatic adenocarcinoma, small cell lung carcinoma, bladder carcinoma, testicular cancer, and so on (Badve et al. 2021). Hamaji found that the thymic carcinoma patients have a lower cumulative incidence of a second malignancy than thymoma patients. (Hamaji et al. 2019a). Apart from the limitation of small sample size, the study by Hamaji et al. also has the limitations of retrospective design, lacking some important data from the database and relatively short follow-up periods with fewer follow-up details (Hamaji et al. 2018, 2019b).
To overcome the problem of a small sample size and assess the incidence and lifetime risk, Surveillance, Epidemiology, and End Results (SEER) database was used to study second malignancies after being diagnosed with thymic carcinoma and thymic NET.
Materials and methods
Patients
The SEER 18-Registries SEER Research Plus Data (2000–2018, Nov 2020 Sub) could be analyzed. In this study, patients with thymic carcinoma were defined with ICD-O-3 codes 8010, 8020–8023, 8032–8033, 8052, 8070–8072, 8074, 8082, 8123, 8140, 8200, 8260, 8310, 8430, 8480, 8560, 8586, and 8589. Patients with thymic NET were defined with ICD-O-3 codes 8012, 8013, 8041, 8044, 8045, 8240, 8246, 8249, and 8574. The patients diagnosed with thymic carcinoma or thymic NET which was not the first cancer in the patient’s life were excluded. Standardized incidence ratio (SIR) which is the ratio of the number of observed cases divided by the number of expected cases was calculated to estimate the relative risk of second malignancy progression. The age-adjusted cancer incidence (per 100,000 persons) was calculated according to the 2000 US standard population census. The age-adjusted cancer incidence in the SEER Population was adopted using the average value of 2000 to 2018. Other parameters such as gender, age, race, and treatment were included. Overall survival (OS) was investigated by the Kaplan–Meier analysis.
The thymic carcinoma and thymic NET are rare, so given the limited sample size of second malignancies after diagnosed with thymic carcinoma and thymic NET, system groups such as respiratory system, endocrine system, and so on were employed to calculate the SIR and the age-adjusted cancer incidence. Furthermore, patients were grouped by different treatments.
Statistical analysis
The two-sample t test was used to examine continuous variables. Statistical significance was considered as two-tailed P values less than 0.05. Pearson’s Chi-squared test statistic was used for analysis of categorical data. The log-rank test was performed to ascertain the differences between the Kaplan–Meier survival curves. The multivariable Cox regression models (including variables of age, sex, ethnicity, and treatment) were used to assess the prognostic effects. The statistical analysis was performed using SPSS 25 (IBM Corp., USA) and GraphPad Prism 8.0 (GraphPad Software, USA). SEER*Stat software (version 8.3.9.2) was utilized to calculate the SIR and the age-adjusted cancer incidence in the SEER population and extract the data of the study cohort from the SEER database. All authors are responsible for statistical review and verification.
Results
The baseline characteristics are listed in Table 1, which summarizes the demographic and characteristics of the 1130 patients with thymic carcinoma and 263 patients with thymic NET from 2000 to 2018, with 48 (65.8%) patients ≥ 60, 41 (56.2%) male, and 50 (58.5%) white patients in the population of thymic carcinoma with second malignancies. Second malignancies were diagnosed 54.26 ± 44.58 months (median 39 months, ranging from 19 to 85.5 months) from the time of the thymic carcinoma diagnosis. The mean age of the thymic carcinoma at diagnosis was 59.57 ± 13.72 years (median age, 61 years old, ranging from 52 to 69 years) and the mean age of the second malignancies at diagnosis was 61.14 ± 12.30 years (median age, 64 years old, ranging from 50 to 69 years). Second malignancies were diagnosed 61.47 ± 52.89 months (median 37 months; ranging from 18 to 116 months) from the time of the thymic NET diagnosis. The mean age of the thymic NET at diagnosis was 54.54 ± 14.98 years (median age, 57 years old, ranging from 43 to 65 years) and the mean age of the second malignancies at diagnosis was 56.32 ± 13.12 years (median age, 59 years old, ranging from 48 to 64 years). Only 3 (4.1%) patients received no treatment among this population. 263 patients with thymic NET are included with 9 (47.4%) patients ≥ 60, 14 (73.7%) male, and 15 (78.9%) white patients in the population of thymic NET with second malignancies. Only one patient did not receive any treatment in this population. Seventy-three patients with thymic carcinoma and 19 patients with thymic NET have 79 and 26 s malignancies, respectively. Five patients have three second malignancies and two patients have four second malignancies in the thymic carcinoma population. Six patients had three second malignancies and one patient had four second malignancies in the thymic NET population.
The overall risk of developing second malignancies in patients with thymic carcinoma increased by 36% (SIR: 1.36, 95% CI 1.08–1.69) and with thymic NET increases by 73% (SIR: 1.73, 95% CI 1.13–2.54). Patients with thymic carcinoma have a particularly high risk of cancers of the respiratory and endocrine systems. Patients with thymic NET demonstrate a particularly high risk of cancers of the breast and endocrine system (Table 2).
As shown in Table 3, the age-adjusted cancer incidence in patients diagnosed with all-site neoplasms after thymic carcinoma is 3058.48 per 100,000, which is 6.58 times that of the age-adjusted cancer incidence in the SEER population (464.5 per 100,000). The age-adjusted incidence of cancer in patients diagnosed with thymic NET is 4178.46 per 100,000. The most common second malignancies in patients with thymic carcinoma are that of cancers of the respiratory system, all lymphatic and hematopoietic diseases, the urinary system, digestive system, and male genital system.
Age at diagnosis is a significant risk factor for the development of second malignancies after the diagnosis of thymic carcinoma in multivariable analyses (Table 4). The time of diagnosis of the second malignancies is set as the endpoint.
In Fig. 1, the thymic carcinoma patients with second malignancies show a statistically significant difference to the patients without second malignancies in the prognosis (OS: p < 0.001). The prognosis of the thymic NET patients has similar results (OS: p = 0.007). The median survival time is 44 months (95% CI 38.95–49.05) in the total thymic carcinoma population. The thymic carcinoma patients with second malignancies show a median survival time of 99 months (95% CI 68.88–129.12). The thymic carcinoma patients without second malignancies have a median survival time of 41 months (95% CI 36.58–45.42). Similarly, the median survival times for the total thymic NET population, the thymic NET with second malignancies population, and the thymic NET without second malignancies population are 65 months (95% CI 51.04–78.96), 163 months (95% CI 59.68–266.32), and 59 months (95% CI 45.00–73.00), respectively.
Cumulative incidence function (CIF) values based on thymic carcinoma and thymic NET are shown in Fig. 2. In patients with thymic carcinoma, CIF of second malignancies is 2.39% at 5 years and 4.69% at 10 years. In patients with thymic NET, CIF of second malignancies is 1.52% at 5 years and 4.18% at 10 years.
Discussion
Thymic carcinoma is a relatively rare malignant tumor that accounts for less than 0.01% of all malignancies diagnosed each year. The rarity of the disease has become an important limiting factor in determining its natural history. Thymic NET that is rarer than thymic carcinoma has the same problem. We attempted to circumvent this limitation by using the SEER database which gathers and publishes data on cancer incidence and lifetime risk for about 28% of the American population.
SIR values for second malignancies in all sites and for each system of cancers in the SEER patients were calculated after diagnosis of thymic carcinoma and thymic NET. This finding indicated that thymic carcinoma has a significantly increased risk for the development of the respiratory system, endocrine system, and all sites. Furthermore, thymic NET shows a distinct increased risk for the development of breast, endocrine system, and all sites. The risk of second malignancies is not increased by different therapies for thymic carcinoma and thymic NET. The present study is the largest of its kind examining the link between thymic carcinoma or thymic NET and second malignancies, looking at cancer incidence after diagnosis.
According to the RARECARE project in Europe, Siesling et al. reported that thymic epithelial tumors have an age-standardized incidence of 0.17 per 100,000 people at risk (Siesling et al. 2012). Based on the data from The Netherlands Cancer Registry Database and The Netherlands National Pathological Archives (PALGA), de Jong et al. found that the incidence of thymic carcinoma is 0.03–0.06 per 100,000 population at risk in The Netherlands (de Jong et al. 2008). According to Gaur et al., the incidence of thymic NET is 0.02 per 100,000 people at risk (Gaur et al. 2010). Yi-Ting Yen et al. found the overall incidence of second malignancies in patients with thymic carcinoma as being 12.2% (10 of 82) (Yen et al. 2011).
We believe that only patients who live longer or with early stage are more likely to have second malignancies, which results in a longer survival period for the patients with second malignancies in Fig. 1.
Existing theories are unable to explain fully those second malignancies diagnosed before thymic carcinoma and thymic NET. There are some possibilities to explain that phenomenon in our opinion. First, the second malignancies diagnosed before thymic malignancies are primary tumors, which are not affected by the thymus. Second, the thymic environment may have already changed a long time before the diagnosis of thymic malignancies, which may be the cause of second malignancies before the thymic malignancies. The reason why thoracic malignancy (as the second malignancy) is common in thymic carcinoma may be the frequent survey of intrathoracic recurrence by chest CT. Our results reveal that thymic NET has higher incidence of endocrine malignancy, which may be due to multiple neuroendocrine neoplasia syndrome associated with thymic carcinoid cases (Ferolla et al. 2005). Thymic NET is may associated with multiple endocrine neoplasia type 1. Meanwhile, a study by NEJM shows that patients who have undergone thymectomy are associated with an increase in autoimmune diseases (Kooshesh et al. 2023). What’s more, age is associated with the hazard of time to onset of second malignancies, so the increase of malignancy incidence with aging may be an important reason.
According to the National Comprehensive Cancer Network guidelines, thymic carcinoma patients have a follow-up period of 5 years and surveillance chest CT should be undertaken to identify disease recurrence after TETs resection every 6 months (Oncology NCPGi. 2017). Patients’ second malignancies were found in different places and at different times in our investigation, as in earlier studies of thymoma (Pan et al. 2001; Evoli et al. 2004; Owe et al. 2010; Weksler et al. 2012; Filosso et al. 2013; Kamata et al. 2017). Because the location of the extrathymic neoplasm is uncertain, adding abdominal CT or other screening methods are options that can be considered.
This study has limitations: although a large database has been applied, the sample sizes remain small given the rareness of thymic carcinoma and thymic NET, thus when calculating the incidence, we used the approach of age adjustment to generalize age-specific rates. However, there was still a lack of patients in some age groups. We introduced the static population data of the United States in 2000 as the standard population, which cannot describe population changes more accurately. Some parts of the data such as stage, grade, and whether cases are accompanied by the paraneoplastic syndrome are missing, which affect the results. Due to the limitations related to the size of the database, the benign tumors cannot be included, which may render our results inaccurate.
Conclusion
Second malignancies are more common in patients with thymic carcinoma and thymic NET, especially in the respiratory system and endocrine system (patients with thymic carcinoma) and in the endocrine system and breast (patients with thymic NET). The age-adjusted cancer incidence of second malignancies increased after being diagnosed with thymic carcinoma and thymic NET. The increased incidence was unrelated to type of treatment delivered. The high incidence of second malignancies makes it important to extend the follow-up period and add abdominal and chest CT periodically. To confirm the association of second malignancies and thymic carcinoma or thymic NET, a larger sample size in such studies is warranted in the future.
Data availability
The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request.
Abbreviations
- NET:
-
Thymic neuroendocrine tumor
- SIR:
-
Standardized incidence ratio
- SEER:
-
Surveillance, Epidemiology, and End Results
- OS:
-
Overall survival
- MG:
-
Myasthenia gravis
- S:
-
Surgery
- R:
-
Radiotherapy
- C:
-
Chemotherapy
References
Ahmad U, Yao X, Detterbeck F et al (2015) Thymic carcinoma outcomes and prognosis: results of an international analysis. J Thorac Cardiovasc Surg 149(95–100):101.e1–2. https://doi.org/10.1016/j.jtcvs.2014.09.124
Badve SS, Dougherty R, Balatico M et al (2021) Thymic carcinomas and second malignancies: a single-center review. Cancers (basel) 13:2472. https://doi.org/10.3390/cancers13102472
Couture MM, Mountain CF (1990) Thymoma. Semin Surg Oncol 6:110–114. https://doi.org/10.1002/ssu.2980060209
de Jong WK, Blaauwgeers JLG, Schaapveld M et al (2008) Thymic epithelial tumours: a population-based study of the incidence, diagnostic procedures and therapy. Eur J Cancer 44:123–130. https://doi.org/10.1016/j.ejca.2007.11.004
Engels EA (2010) Epidemiology of thymoma and associated malignancies. J Thorac Oncol 5:S260-265. https://doi.org/10.1097/JTO.0b013e3181f1f62d
Evoli A, Punzi C, Marsili F et al (2004) Extrathymic malignancies in patients with thymoma. Ann Oncol 15:692–693. https://doi.org/10.1093/annonc/mdh155
Ferolla P, Falchetti A, Filosso P et al (2005) Thymic neuroendocrine carcinoma (carcinoid) in multiple endocrine neoplasia type 1 syndrome: the Italian series. J Clin Endocrinol Metab 90:2603–2609. https://doi.org/10.1210/jc.2004-1155
Filosso PL, Galassi C, Ruffini E et al (2013) Thymoma and the increased risk of developing extrathymic malignancies: a multicentre study. Eur J Cardiothorac Surg 44:219–224. https://doi.org/10.1093/ejcts/ezs663. (discussion 224)
Gaur P, Leary C, Yao JC (2010) Thymic neuroendocrine tumors: a SEER database analysis of 160 patients. Ann Surg 251:1117–1121. https://doi.org/10.1097/SLA.0b013e3181dd4ec4
Gray GF, Gutowski WT (1979) Thymoma. A clinicopathologic study of 54 cases. Am J Surg Pathol 3:235–249
Hamaji M, Sozu T, Machida R et al (2018) Second malignancy versus recurrence after complete resection of thymoma. Asian Cardiovasc Thorac Ann 26:290–295. https://doi.org/10.1177/0218492318765872
Hamaji M, Kawaguchi A, Omasa M et al (2019a) Low incidence of and mortality from a second malignancy after resection of thymic carcinoma†. Interact Cardiovasc Thorac Surg 28:375–379. https://doi.org/10.1093/icvts/ivy260
Hamaji M, Sozu T, Machida R et al (2019b) Mortality from extrathymic malignancy after thymic tumour resections: incidences and risk factors. Interact Cardiovasc Thorac Surg 29:729–736. https://doi.org/10.1093/icvts/ivz177
Kamata T, Yoshida S, Wada H et al (2017) Extrathymic malignancies associated with thymoma: a forty-year experience at a single institution. Interact Cardiovasc Thorac Surg 24:576–581. https://doi.org/10.1093/icvts/ivw354
Kooshesh KA, Foy BH, Sykes DB et al (2023) Health consequences of thymus removal in adults. N Engl J Med 389:406–417. https://doi.org/10.1056/NEJMoa2302892
LeGolvan DP, Abell MR (1977) Thymomas. Cancer 39:2142–2157. https://doi.org/10.1002/1097-0142(197705)39:5%3c2142::aid-cncr2820390531%3e3.0.co;2-q
Lewis JE, Wick MR, Scheithauer BW et al (1987) Thymoma. A clinicopathologic review. Cancer 60:2727–2743. https://doi.org/10.1002/1097-0142(19871201)60:11%3c2727::aid-cncr2820601125%3e3.0.co;2-d
Oncology NCPGi (2017) Thymomas and thymic carcinomas
Owe JF, Cvancarova M, Romi F, Gilhus NE (2010) Extrathymic malignancies in thymoma patients with and without myasthenia gravis. J Neurol Sci 290:66–69. https://doi.org/10.1016/j.jns.2009.11.006
Pan CC, Chen PC, Wang LS et al (2001) Thymoma is associated with an increased risk of second malignancy. Cancer 92:2406–2411. https://doi.org/10.1002/1097-0142(20011101)92:9%3c2406::aid-cncr1589%3e3.0.co;2-7
Siesling S, van der Zwan JM, Izarzugaza I et al (2012) Rare thoracic cancers, including peritoneum mesothelioma. Eur J Cancer 48:949–960. https://doi.org/10.1016/j.ejca.2012.02.047
Venuta F, Anile M, Diso D et al (2010) Thymoma and thymic carcinoma. Eur J Cardiothorac Surg 37:13–25. https://doi.org/10.1016/j.ejcts.2009.05.038
Weksler B, Nason KS, Mackey D et al (2012) Thymomas and extrathymic cancers. Ann Thorac Surg 93:884–888. https://doi.org/10.1016/j.athoracsur.2011.05.089
Welsh JS, Wilkins KB, Green R et al (2000) Association between thymoma and second neoplasms. JAMA 283:1142–1143. https://doi.org/10.1001/jama.283.9.1142
Wilkins KB, Sheikh E, Green R et al (1999) Clinical and pathologic predictors of survival in patients with thymoma. Ann Surg 230:562–572. https://doi.org/10.1097/00000658-199910000-00012. (discussion 572-574)
Yen Y-T, Lai W-W, Wu M-H et al (2011) Thymic neuroendocrine carcinoma and thymoma are both associated with increased risk of extrathymic malignancy: a 20-year review of a single institution. Ann Thorac Surg 91:219–225. https://doi.org/10.1016/j.athoracsur.2010.09.025
Funding
This study was supported by grants from the National Key Research Project of China (no. 2017YFC0113502), Key Research Project of Sichuan Province (no. 2020YFS0249) and 1·3·5 project for disciplines of excellence-Clinical Research Incubation Project, West China Hospital, Sichuan University (2021HXFH056).
Author information
Authors and Affiliations
Contributions
GQ and FW contributed equally to this work. Conceptualization: GQ; methodology, formal analysis and investigation: GQ and FW; writing—original draft preparation: GQ and FW; writing—review and editing: all authors; resources: GQ; supervision: YW and all authors commented on previous versions of the manuscript. All authors read and approved the final manuscript.
Corresponding author
Ethics declarations
Conflict of interest
All authors report this study was supported by grants from the National Key Research Project of China (no. 2017YFC0113502), Key Research Project of Sichuan Province (no. 2020YFS0249) and 1·3·5 project for disciplines of excellence–Clinical Research Incubation Project, West China Hospital, Sichuan University (2021HXFH056). The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.
Ethics statement
This study was approved by the Ethics Committee of West China Hospital (2021-385). Patient consent is not required because the data are sourced from the SEER database.
Consent to publish
Not applicable.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Qiu, G., Wang, F. & Wang, Y. Incidence of second malignancies in patients with thymic carcinoma and thymic neuroendocrine tumor. J Cancer Res Clin Oncol 150, 11 (2024). https://doi.org/10.1007/s00432-023-05522-3
Received:
Accepted:
Published:
DOI: https://doi.org/10.1007/s00432-023-05522-3