Klinefelter syndrome in males with germ cell tumors: A report from the children’s oncology group

Lindsay A. Williams, Nathan Pankratz, John Lane, Mark Krailo, Michelle Roesler, Michaela Richardson, A. Lindsay Frazier, James F. Amatruda, Jenny N. Poynter

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

Background: Males with Klinefelter syndrome (KS) (47,XXY) may be more likely to develop germ cell tumors (GCTs), particularly mediastinal GCTs. To date, there are no reports characterizing the prevalence of KS among male GCT cases. Methods: The authors used array genotyping data from a Children’s Oncology Group epidemiology study to estimate the prevalence of KS in males with GCTs (433 males aged birth-19 years). Using Fisher’s exact tests, the authors examined differences in age at diagnosis, race/ethnicity, tumor location and histology, and several birth characteristics between cases of KS-GCT and GCT cases without chromosomal abnormalities. Using publicly available data, the authors estimated the 1-year risk, risk ratio, and corresponding 95% confidence interval of GCTs among KS cases. Results: Based on analysis of array genotyping data, 3% of male GCT cases (13 cases) had KS. The additional X chromosome was of maternal origin in 7 of the 13 cases. Of these 13 KS cases, 5 of 9 KS-GCT cases with parental questionnaire data (56%) reported a diagnosis of KS. No significant differences were observed with regard to patient or birth characteristics between KS-GCT and non–KS-GCT cases. KS-GCT cases were significantly more likely to be diagnosed with mediastinal tumors than non–KS-GCT cases (P<.01). The authors estimated the risk of developing a GCT among males with KS to be 0.00025, or 1 per 4000 males (risk ratio, 18.8; 95% confidence interval, 11.7-30.0). Conclusions: Compared with males without chromosomal abnormalities, males with KS are more likely to be diagnosed with a mediastinal GCT. The presence of KS should be considered in males with a diagnosis of mediastinal GCT.

Original languageEnglish (US)
JournalCancer
DOIs
StateAccepted/In press - Jan 1 2018

Fingerprint

Klinefelter Syndrome
Germ Cell and Embryonal Neoplasms
Parturition
Male Germ Cell Tumor
Chromosome Aberrations
Odds Ratio
Confidence Intervals
X Chromosome

Keywords

  • epidemiology
  • germ cell tumors
  • histology
  • Klinefelter syndrome
  • mediastinal tumors

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

Cite this

Williams, L. A., Pankratz, N., Lane, J., Krailo, M., Roesler, M., Richardson, M., ... Poynter, J. N. (Accepted/In press). Klinefelter syndrome in males with germ cell tumors: A report from the children’s oncology group. Cancer. https://doi.org/10.1002/cncr.31667

Klinefelter syndrome in males with germ cell tumors : A report from the children’s oncology group. / Williams, Lindsay A.; Pankratz, Nathan; Lane, John; Krailo, Mark; Roesler, Michelle; Richardson, Michaela; Lindsay Frazier, A.; Amatruda, James F.; Poynter, Jenny N.

In: Cancer, 01.01.2018.

Research output: Contribution to journalArticle

Williams, LA, Pankratz, N, Lane, J, Krailo, M, Roesler, M, Richardson, M, Lindsay Frazier, A, Amatruda, JF & Poynter, JN 2018, 'Klinefelter syndrome in males with germ cell tumors: A report from the children’s oncology group', Cancer. https://doi.org/10.1002/cncr.31667
Williams, Lindsay A. ; Pankratz, Nathan ; Lane, John ; Krailo, Mark ; Roesler, Michelle ; Richardson, Michaela ; Lindsay Frazier, A. ; Amatruda, James F. ; Poynter, Jenny N. / Klinefelter syndrome in males with germ cell tumors : A report from the children’s oncology group. In: Cancer. 2018.
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abstract = "Background: Males with Klinefelter syndrome (KS) (47,XXY) may be more likely to develop germ cell tumors (GCTs), particularly mediastinal GCTs. To date, there are no reports characterizing the prevalence of KS among male GCT cases. Methods: The authors used array genotyping data from a Children’s Oncology Group epidemiology study to estimate the prevalence of KS in males with GCTs (433 males aged birth-19 years). Using Fisher’s exact tests, the authors examined differences in age at diagnosis, race/ethnicity, tumor location and histology, and several birth characteristics between cases of KS-GCT and GCT cases without chromosomal abnormalities. Using publicly available data, the authors estimated the 1-year risk, risk ratio, and corresponding 95{\%} confidence interval of GCTs among KS cases. Results: Based on analysis of array genotyping data, 3{\%} of male GCT cases (13 cases) had KS. The additional X chromosome was of maternal origin in 7 of the 13 cases. Of these 13 KS cases, 5 of 9 KS-GCT cases with parental questionnaire data (56{\%}) reported a diagnosis of KS. No significant differences were observed with regard to patient or birth characteristics between KS-GCT and non–KS-GCT cases. KS-GCT cases were significantly more likely to be diagnosed with mediastinal tumors than non–KS-GCT cases (P<.01). The authors estimated the risk of developing a GCT among males with KS to be 0.00025, or 1 per 4000 males (risk ratio, 18.8; 95{\%} confidence interval, 11.7-30.0). Conclusions: Compared with males without chromosomal abnormalities, males with KS are more likely to be diagnosed with a mediastinal GCT. The presence of KS should be considered in males with a diagnosis of mediastinal GCT.",
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AU - Lane, John

AU - Krailo, Mark

AU - Roesler, Michelle

AU - Richardson, Michaela

AU - Lindsay Frazier, A.

AU - Amatruda, James F.

AU - Poynter, Jenny N.

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N2 - Background: Males with Klinefelter syndrome (KS) (47,XXY) may be more likely to develop germ cell tumors (GCTs), particularly mediastinal GCTs. To date, there are no reports characterizing the prevalence of KS among male GCT cases. Methods: The authors used array genotyping data from a Children’s Oncology Group epidemiology study to estimate the prevalence of KS in males with GCTs (433 males aged birth-19 years). Using Fisher’s exact tests, the authors examined differences in age at diagnosis, race/ethnicity, tumor location and histology, and several birth characteristics between cases of KS-GCT and GCT cases without chromosomal abnormalities. Using publicly available data, the authors estimated the 1-year risk, risk ratio, and corresponding 95% confidence interval of GCTs among KS cases. Results: Based on analysis of array genotyping data, 3% of male GCT cases (13 cases) had KS. The additional X chromosome was of maternal origin in 7 of the 13 cases. Of these 13 KS cases, 5 of 9 KS-GCT cases with parental questionnaire data (56%) reported a diagnosis of KS. No significant differences were observed with regard to patient or birth characteristics between KS-GCT and non–KS-GCT cases. KS-GCT cases were significantly more likely to be diagnosed with mediastinal tumors than non–KS-GCT cases (P<.01). The authors estimated the risk of developing a GCT among males with KS to be 0.00025, or 1 per 4000 males (risk ratio, 18.8; 95% confidence interval, 11.7-30.0). Conclusions: Compared with males without chromosomal abnormalities, males with KS are more likely to be diagnosed with a mediastinal GCT. The presence of KS should be considered in males with a diagnosis of mediastinal GCT.

AB - Background: Males with Klinefelter syndrome (KS) (47,XXY) may be more likely to develop germ cell tumors (GCTs), particularly mediastinal GCTs. To date, there are no reports characterizing the prevalence of KS among male GCT cases. Methods: The authors used array genotyping data from a Children’s Oncology Group epidemiology study to estimate the prevalence of KS in males with GCTs (433 males aged birth-19 years). Using Fisher’s exact tests, the authors examined differences in age at diagnosis, race/ethnicity, tumor location and histology, and several birth characteristics between cases of KS-GCT and GCT cases without chromosomal abnormalities. Using publicly available data, the authors estimated the 1-year risk, risk ratio, and corresponding 95% confidence interval of GCTs among KS cases. Results: Based on analysis of array genotyping data, 3% of male GCT cases (13 cases) had KS. The additional X chromosome was of maternal origin in 7 of the 13 cases. Of these 13 KS cases, 5 of 9 KS-GCT cases with parental questionnaire data (56%) reported a diagnosis of KS. No significant differences were observed with regard to patient or birth characteristics between KS-GCT and non–KS-GCT cases. KS-GCT cases were significantly more likely to be diagnosed with mediastinal tumors than non–KS-GCT cases (P<.01). The authors estimated the risk of developing a GCT among males with KS to be 0.00025, or 1 per 4000 males (risk ratio, 18.8; 95% confidence interval, 11.7-30.0). Conclusions: Compared with males without chromosomal abnormalities, males with KS are more likely to be diagnosed with a mediastinal GCT. The presence of KS should be considered in males with a diagnosis of mediastinal GCT.

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