Literature DB >> 28400402

Molecular targeted therapies in adrenal, pituitary and parathyroid malignancies.

Anna Angelousi1, Georgios K Dimitriadis2, Georgios Zografos3, Svenja Nölting4, Gregory Kaltsas5,2,6, Ashley Grossman6.   

Abstract

Tumourigenesis is a relatively common event in endocrine tissues. Currently, specific guidelines have been developed for common malignant endocrine tumours, which also incorporate advances in molecular targeted therapies (MTT), as in thyroid cancer and in gastrointestinal neuroendocrine malignancies. However, there is little information regarding the role and efficacy of MTT in the relatively rare malignant endocrine tumours mainly involving the adrenal medulla, adrenal cortex, pituitary, and parathyroid glands. Due to the rarity of these tumours and the lack of prospective studies, current guidelines are mostly based on retrospective data derived from surgical, locoregional and ablative therapies, and studies with systemic chemotherapy. In addition, in many of these malignancies the prognosis remains poor with individual patients responding differently to currently available treatments, necessitating the development of new personalised therapeutic strategies. Recently, major advances in the molecular understanding of endocrine tumours based on genomic, epigenomic, and transcriptome analysis have emerged, resulting in new insights into their pathogenesis and molecular pathology. This in turn has led to the use of novel MTTs in increasing numbers of patients. In this review, we aim to present currently existing and evolving data using MTT in the treatment of adrenal, pituitary and malignant parathyroid tumours, and explore the current utility and effectiveness of such therapies and their future evolution.
© 2017 Society for Endocrinology.

Entities:  

Keywords:  adrenocortical cancer; molecular genetics; paraganglioma; parathyroid carcinoma; phaeochromocytoma; pituitary carcinoma; tyrosine kinase inhibitor

Mesh:

Year:  2017        PMID: 28400402     DOI: 10.1530/ERC-16-0542

Source DB:  PubMed          Journal:  Endocr Relat Cancer        ISSN: 1351-0088            Impact factor:   5.678


  6 in total

Review 1.  Metastatic Phaeochromocytoma: Spinning Towards More Promising Treatment Options.

Authors:  Svenja Nölting; Ashley Grossman; Karel Pacak
Journal:  Exp Clin Endocrinol Diabetes       Date:  2018-09-20       Impact factor: 2.949

Review 2.  Pheochromocytomas and Hypertension.

Authors:  Joseph M Pappachan; Nyo Nyo Tun; Ganesan Arunagirinathan; Ravinder Sodi; Fahmy W F Hanna
Journal:  Curr Hypertens Rep       Date:  2018-01-22       Impact factor: 5.369

3.  Special Issue: Present and Future of Personalised Medicine for Endocrine Cancers.

Authors:  Cristina L Ronchi; Barbara Altieri
Journal:  J Pers Med       Date:  2022-04-29

4.  Nutlin-3a as a novel anticancer agent for adrenocortical carcinoma with CTNNB1 mutation.

Authors:  Wen Hui; Shenghua Liu; Jie Zheng; Zujun Fang; Qiang Ding; Chenchen Feng
Journal:  Cancer Med       Date:  2018-03-13       Impact factor: 4.452

5.  Parathyroid carcinoma in a 13-year-old girl with a long-term survival.

Authors:  Yoko Omi; Tomoko Yamamoto; Yoji Nagashima; Koichiro Abe; Kumiko Karasawa; Yukichi Tanaka; Takahiro Okamoto
Journal:  Surg Case Rep       Date:  2020-06-22

6.  Gonadotrophin-releasing hormone agonist-induced pituitary adenoma apoplexy and casual finding of a parathyroid carcinoma: A case report and review of literature.

Authors:  Vanessa Triviño; Olga Fidalgo; Antía Juane; Jorge Pombo; Fernando Cordido
Journal:  World J Clin Cases       Date:  2019-10-26       Impact factor: 1.337

  6 in total

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