Revised European Society of Endocrinology Clinical Practice Guideline for the management of aggressive pituitary tumours and pituitary carcinomas

Pituitary tumours, originating from endocrine cells of the anterior pituitary, are quite common, and in most cases well-controlled by surgery or medical treatment. However, a small subset of pituitary tumours presents with multiple local recurrences or tumour progression despite combined surgical, m...

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Published inEuropean journal of endocrinology Vol. 192; no. 6; pp. G1 - G34
Main Authors Raverot, Gerald, Burman, Pia, Abreu, Ana Paula, Heaney, Anthony P, van Hulsteijn, Leonie, Lin, Andrew L, Marcus, Hani, McCormack, Ann, Minniti, Giuseppe, Petersenn, Stephan, Popovic, Vera, Theodoropoulou, Marily, Trouillas, Jacqueline, Dekkers, Olaf M
Format Journal Article
LanguageEnglish
Published England Oxford University Press 01.06.2025
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Online AccessGet full text
ISSN0804-4643
1479-683X
1479-683X
DOI10.1093/ejendo/lvaf100

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Abstract Pituitary tumours, originating from endocrine cells of the anterior pituitary, are quite common, and in most cases well-controlled by surgery or medical treatment. However, a small subset of pituitary tumours presents with multiple local recurrences or tumour progression despite combined surgical, medical or radiotherapeutic treatment. These are known as aggressive pituitary tumours (APT); also called aggressive pituitary neuroendocrine tumours (PitNETs); or, in the rare case of metastases, pituitary carcinomas (PC) or metastatic PitNETs. Early identification of APT is challenging but is of major clinical importance as they are associated with an increased morbidity and mortality even in the absence of metastases. Here, we provide a revision of the first international, interdisciplinary European Society of Endocrinology (ESE) clinical practice guideline on APTs and PC (2018). Since publication of the 2018 guideline, results from the second ESE survey on APT and PC were published, and more data on APT treatment, including temozolomide, immune checkpoint inhibitors and bevacizumab, emerged. These data are reviewed in this guideline and translated into a practical algorithm to guide APT and PC management. Furthermore, standardized reporting of imaging and histopathological investigations of these tumours is proposed, and the role of molecular analysis is discussed. Last, a section is dedicated to special circumstances such as APT in pregnancy.
AbstractList Pituitary tumours, originating from endocrine cells of the anterior pituitary, are quite common, and in most cases well-controlled by surgery or medical treatment. However, a small subset of pituitary tumours presents with multiple local recurrences or tumour progression despite combined surgical, medical or radiotherapeutic treatment. These are known as aggressive pituitary tumours (APT); also called aggressive pituitary neuroendocrine tumours (PitNETs); or, in the rare case of metastases, pituitary carcinomas (PC) or metastatic PitNETs. Early identification of APT is challenging but is of major clinical importance as they are associated with an increased morbidity and mortality even in the absence of metastases. Here, we provide a revision of the first international, interdisciplinary European Society of Endocrinology (ESE) clinical practice guideline on APTs and PC (2018). Since publication of the 2018 guideline, results from the second ESE survey on APT and PC were published, and more data on APT treatment, including temozolomide, immune checkpoint inhibitors and bevacizumab, emerged. These data are reviewed in this guideline and translated into a practical algorithm to guide APT and PC management. Furthermore, standardized reporting of imaging and histopathological investigations of these tumours is proposed, and the role of molecular analysis is discussed. Last, a section is dedicated to special circumstances such as APT in pregnancy.
Pituitary tumours, originating from endocrine cells of the anterior pituitary, are quite common, and in most cases well-controlled by surgery or medical treatment. However, a small subset of pituitary tumours presents with multiple local recurrences or tumour progression despite combined surgical, medical or radiotherapeutic treatment. These are known as aggressive pituitary tumours (APT); also called aggressive pituitary neuroendocrine tumours (PitNETs); or, in the rare case of metastases, pituitary carcinomas (PC) or metastatic PitNETs. Early identification of APT is challenging but is of major clinical importance as they are associated with an increased morbidity and mortality even in the absence of metastases. Here, we provide a revision of the first international, interdisciplinary European Society of Endocrinology (ESE) clinical practice guideline on APTs and PC (2018). Since publication of the 2018 guideline, results from the second ESE survey on APT and PC were published, and more data on APT treatment, including temozolomide, immune checkpoint inhibitors and bevacizumab, emerged. These data are reviewed in this guideline and translated into a practical algorithm to guide APT and PC management. Furthermore, standardized reporting of imaging and histopathological investigations of these tumours is proposed, and the role of molecular analysis is discussed. Last, a section is dedicated to special circumstances such as APT in pregnancy.Pituitary tumours, originating from endocrine cells of the anterior pituitary, are quite common, and in most cases well-controlled by surgery or medical treatment. However, a small subset of pituitary tumours presents with multiple local recurrences or tumour progression despite combined surgical, medical or radiotherapeutic treatment. These are known as aggressive pituitary tumours (APT); also called aggressive pituitary neuroendocrine tumours (PitNETs); or, in the rare case of metastases, pituitary carcinomas (PC) or metastatic PitNETs. Early identification of APT is challenging but is of major clinical importance as they are associated with an increased morbidity and mortality even in the absence of metastases. Here, we provide a revision of the first international, interdisciplinary European Society of Endocrinology (ESE) clinical practice guideline on APTs and PC (2018). Since publication of the 2018 guideline, results from the second ESE survey on APT and PC were published, and more data on APT treatment, including temozolomide, immune checkpoint inhibitors and bevacizumab, emerged. These data are reviewed in this guideline and translated into a practical algorithm to guide APT and PC management. Furthermore, standardized reporting of imaging and histopathological investigations of these tumours is proposed, and the role of molecular analysis is discussed. Last, a section is dedicated to special circumstances such as APT in pregnancy.
Author Abreu, Ana Paula
Petersenn, Stephan
Theodoropoulou, Marily
Dekkers, Olaf M
Popovic, Vera
Trouillas, Jacqueline
McCormack, Ann
Minniti, Giuseppe
Heaney, Anthony P
Raverot, Gerald
Burman, Pia
Lin, Andrew L
van Hulsteijn, Leonie
Marcus, Hani
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ISSN 0804-4643
1479-683X
IngestDate Fri Jun 13 18:14:08 EDT 2025
Mon Sep 15 09:10:48 EDT 2025
Tue Jul 01 05:31:16 EDT 2025
Thu Jul 03 08:39:36 EDT 2025
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Issue 6
Keywords aggressive pituitary tumour-Pituitary carcinoma
pituitary adenoma
prognosis
therapy
Language English
License https://creativecommons.org/licenses/by-nc/4.0
The Author(s) 2025. Published by Oxford University Press on behalf of European Society of Endocrinology.
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Snippet Pituitary tumours, originating from endocrine cells of the anterior pituitary, are quite common, and in most cases well-controlled by surgery or medical...
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SubjectTerms Bevacizumab
Brain tumors
Carcinoma
Clinical medicine
Clinical practice guidelines
Disease Management
Endocrinology
Endocrinology - standards
Europe - epidemiology
Female
Humans
Immune checkpoint inhibitors
Medical treatment
Metastases
Metastasis
Morbidity
Neuroendocrine tumors
Neuroendocrine Tumors - pathology
Neuroendocrine Tumors - therapy
Pituitary (anterior)
Pituitary Neoplasms - diagnosis
Pituitary Neoplasms - pathology
Pituitary Neoplasms - therapy
Practice Guidelines as Topic - standards
Societies, Medical - standards
Temozolomide
Tumors
Title Revised European Society of Endocrinology Clinical Practice Guideline for the management of aggressive pituitary tumours and pituitary carcinomas
URI https://www.ncbi.nlm.nih.gov/pubmed/40506054
https://www.proquest.com/docview/3248888492
https://www.proquest.com/docview/3218471226
Volume 192
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