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 in | European journal of endocrinology Vol. 192; no. 6; pp. G1 - G34 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Oxford University Press
01.06.2025
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Subjects | |
Online Access | Get full text |
ISSN | 0804-4643 1479-683X 1479-683X |
DOI | 10.1093/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. |
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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 |
Author_xml | – sequence: 1 givenname: Gerald orcidid: 0000-0002-9517-338X surname: Raverot fullname: Raverot, Gerald – sequence: 2 givenname: Pia orcidid: 0000-0002-4844-8336 surname: Burman fullname: Burman, Pia – sequence: 3 givenname: Ana Paula orcidid: 0000-0002-5505-0852 surname: Abreu fullname: Abreu, Ana Paula – sequence: 4 givenname: Anthony P orcidid: 0000-0003-3865-0810 surname: Heaney fullname: Heaney, Anthony P – sequence: 5 givenname: Leonie orcidid: 0000-0002-2617-5429 surname: van Hulsteijn fullname: van Hulsteijn, Leonie – sequence: 6 givenname: Andrew L orcidid: 0000-0003-0659-261X surname: Lin fullname: Lin, Andrew L – sequence: 7 givenname: Hani surname: Marcus fullname: Marcus, Hani – sequence: 8 givenname: Ann orcidid: 0000-0002-2859-5566 surname: McCormack fullname: McCormack, Ann – sequence: 9 givenname: Giuseppe surname: Minniti fullname: Minniti, Giuseppe – sequence: 10 givenname: Stephan surname: Petersenn fullname: Petersenn, Stephan – sequence: 11 givenname: Vera surname: Popovic fullname: Popovic, Vera – sequence: 12 givenname: Marily orcidid: 0000-0002-7378-4374 surname: Theodoropoulou fullname: Theodoropoulou, Marily – sequence: 13 givenname: Jacqueline surname: Trouillas fullname: Trouillas, Jacqueline – sequence: 14 givenname: Olaf M orcidid: 0000-0002-1333-7580 surname: Dekkers fullname: Dekkers, Olaf M |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/40506054$$D View this record in MEDLINE/PubMed |
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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 |
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