- 1Bristol Medical School, Department of Translational Health Sciences, University of Bristol, Bristol, United Kingdom
- 2Department of Clinical and Experimental Medicine, University of Catania, Catania, Italy
Editorial on the Research Topic
Insights in cancer endocrinology: 2022
It is our pleasure to introduce this Research Topic entitled “Insights in cancer endocrinology: 2022” that particularly highlights some of the issues surrounding rarer endocrine malignancies, such as parathyroid carcinoma (PC) and medullary thyroid (MT) cancer.
Neuroendocrine neoplasms (NENs) can occur in different locations in the body, for example the pancreas and lung. They are composed of two types: well-differentiated and low-proliferating NENs - neuroendocrine tumours (NETs) and poorly differentiated, highly proliferating NENs- neuroendocrine carcinomas (NECs). Puliafito et al. conducted a retrospective study that included 70 patients with lung NECs to compare the outcome data, including disease control rate, overall and progression-free survival for patients treated with either cisplatin or carboplatin.
Thyroid cancer (TC) is the most common endocrine malignancy accounting for 586202 new cases and 43646 deaths in 2020 (1). The identification of four main sub-types of TC, including differentiated, poorly differentiated, medullary, and anaplastic, has led to a better understanding of the molecular progression of the disease. The important contribution of tyrosine kinase inhibitors (TKIs) in the treatment of TC is highlighted in a comprehensive review by Puliafito et al., in which clinical trials demonstrating improved progression-free survival are cited along with a discussion on their associated toxicities and how this may be managed.
Medullary TC is the rarest sub-type accounting for approximately 4% of all TCs (2) and in their overview, Zhang et al. appraise the current guidelines for the management of MTC. Located on or near the thyroid gland are the parathyroid glands. Primary hyperparathyroidism (PHPT) occurs when one or more of these glands over-secrete parathyroid hormone (PTH). Barale et al. focus on two rare causes of PHPT, PC and atypical carcinoma (AC). Their study aimed to identify factors particular to these carcinomas to enable the prediction of the clinical outcome of PC or AC following surgery.
We have enjoyed hosting this exciting Research Topic and we thank all the authors for their excellent contributions.
Author contributions
CP wrote the editorial. CP and AB commented on a draft and agreed to the final version.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
The handling editor JH declared a shared affiliation with the author CP at the time of review.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
References
1. Sung H, Ferlay J, Siegel RL, Laversanne M, Soerjomataram I, Jemal A, et al. Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin (2021) 71(3):209–49. doi: 10.3322/caac.21660
Keywords: endocrine malignancies, medullary thyroid cancer, rare endocrine malignancies, neuroendocrine neoplasms (NENs), parathyroid carcinoma
Citation: Perks CM and Belfiore A (2023) Editorial: Insights in cancer endocrinology: 2022. Front. Endocrinol. 14:1236887. doi: 10.3389/fendo.2023.1236887
Received: 08 June 2023; Accepted: 26 June 2023;
Published: 07 July 2023.
Edited and Reviewed by:
Jeff M. P. Holly, University of Bristol, United KingdomCopyright © 2023 Perks and Belfiore. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Claire M. Perks, Claire.M.Perks@bristol.ac.uk