Literature DB >> 18327035

The need for patients' endocrine function vigilance following treatment of head and neck cancer.

Remco de Bree1, Paul Lips, C René Leemans.   

Abstract

PURPOSE OF REVIEW: The aim of this article is to examine the need for screening of endocrine dysfunction following treatment of head and neck cancer. RECENT
FINDINGS: The incidence of occult hypothyroidism following treatment of head and neck cancer is high. Patients who develop hypothyroidism after treatment may have an increased survival compared with patients who did not become hypothyroid. Because of the growing body of evidence that supports a permissive role for thyroid hormone in the growth of certain solid tumours thyroid hormone replacement therapy may not be indicated in patients with subclinical hypothyroidism and prior or current cancer. Although the incidence of hypoparathyroidism after treatment for head and neck cancer is low, testing of serum calcium is easily performed during thyroid function evaluation. The incidence of hypopituitarism after irradiation of the nasopharynx or skull base is very high warranting regular evaluation of endocrine functions.
SUMMARY: Owing to the high incidence of endocrine dysfunction, all head and neck cancer patients who undergo treatment of the lower neck, nasopharynx or base of skull need regular endocrine evaluation during long-term follow-up to determine the need to start hormone replacement therapy and maintain optimal quality of life.

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Mesh:

Year:  2008        PMID: 18327035     DOI: 10.1097/MOO.0b013e3282f4479d

Source DB:  PubMed          Journal:  Curr Opin Otolaryngol Head Neck Surg        ISSN: 1068-9508            Impact factor:   2.064


  4 in total

1.  Rationale behind thyroidectomy in total laryngectomy: analysis of endocrine insufficiency and oncological outcomes.

Authors:  Smriti Panda; Rajeev Kumar; Abhilash Konkimalla; Alok Thakar; Chirom Amit Singh; Kapil Sikka; Suresh C Sharma; Aanchal Kakkar; Suman Bhasker
Journal:  Indian J Surg Oncol       Date:  2019-05-22

2.  Whole Exome Sequencing Points towards a Multi-Gene Synergistic Action in the Pathogenesis of Congenital Combined Pituitary Hormone Deficiency.

Authors:  Amalia Sertedaki; Elizabeth Barbara Tatsi; Ioannis Anargyros Vasilakis; Irene Fylaktou; Eirini Nikaina; Nicoletta Iacovidou; Tania Siahanidou; Christina Kanaka-Gantenbein
Journal:  Cells       Date:  2022-06-30       Impact factor: 7.666

Review 3.  Genetics of Combined Pituitary Hormone Deficiency: Roadmap into the Genome Era.

Authors:  Qing Fang; Akima S George; Michelle L Brinkmeier; Amanda H Mortensen; Peter Gergics; Leonard Y M Cheung; Alexandre Z Daly; Adnan Ajmal; María Ines Pérez Millán; A Bilge Ozel; Jacob O Kitzman; Ryan E Mills; Jun Z Li; Sally A Camper
Journal:  Endocr Rev       Date:  2016-11-09       Impact factor: 19.871

4.  The effect of substitution therapy on symptoms in patients with hypothyroidism following treatment for laryngeal and hypopharyngeal carcinomas.

Authors:  A M Lo Galbo; I M Verdonck-De Leeuw; P Lips; D J Kuik; C R Leemans; R De Bree
Journal:  Acta Otorhinolaryngol Ital       Date:  2013-08       Impact factor: 2.124

  4 in total

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