European Thyroid Journal (Jan 2023)

Puberty and sex in pediatric thyroid cancer: could expression of estrogen and progesterone receptors affect prognosis?

  • Julia Ramalho Amalio da Silva Breder,
  • Paulo Alonso Garcia Alves Jr,
  • Mario Lucio Araújo Jr,
  • Barbara Pires,
  • Priscila Valverde,
  • Daniel Alves Bulzico,
  • Fernanda Andrade Accioly,
  • Rossana Corbo,
  • Mario Vaisman,
  • Fernanda Vaisman

DOI
https://doi.org/10.1530/ETJ-21-0090
Journal volume & issue
Vol. 11, no. 2
pp. 1 – 9

Abstract

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Objective: A sharp increase in pediatric thyroid cancer incidence is observed during adolescence, driven mainly by girls. Differences in disease pres entation across sexual maturity stages raise the question of whether sex steroids have a role in the heterogeneity. The aims of this study were to analyze the influe nce of puberty and sex on clinical presentation and prognosis and to evaluate the correlation between the expression of sex hormone receptors. Design and methods: Clinical records and immunohistochemical of specimens from 79 patients were analyzed. Puberty was analyzed by two criteria: end of puberty and beginning, in which the age of 10 was the cutoff. Results: Postpubertal were more frequently classified as having low-risk disease and a lower frequency of persistent disease, especially when the completion of puberty was used as the criteria. Male sex was associated with a higher ris k of persistent disease at the end of the observation period. Estrogen receptor α positivity was low in the entire sample, while progesterone receptor positivity was positive in 30% of the cases. Female hormone receptor expression was not associated with sex, American Thyroid Association risk score, persistent structural disease, or pubertal status. Conclusion: Our study showed that the completion of puberty correlated best with the clinical behaviour of pediatric thyroid cancer. It was also shown that postpubertal patients have a less aggressive initial presentation and better outcomes. However, this observation could not be explained by the expression of estrogen and progesterone receptors in the primary tumors.

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