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      High prevalence of anterior pituitary deficiencies after cranial radiation therapy for skull base meningiomas

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          Abstract

          Background

          Cranial irradiation represents one of the first line treatment proposed in skull base meningiomas. While cranial irradiation is associated with a high risk of secondary hypopituitarism, few studies focused on the specific location of skull base meningiomas.

          Methods

          Fifty-two adults receiving photon-beam therapy for skull base meningiomas between 2003 and 2014 in our Institution were included. Anterior pituitary (ACTH, FSH, GH, LH, TSH and prolactin) as well as corresponding peripheral hormones (8 am-Cortisol, IGF-1, fT3, fT4, 17βestradiol or testosterone) were biologically screened before radiotherapy (baseline), then yearly until March 2019. The pituitary gland (PG) was delineated on CT and the mean dose delivered to it was calculated.

          Results

          Mean age at diagnosis was 56 +/− 14 years. Median follow-up was 7 years. Up to 60% of patients developed at least ≥2 pituitary deficiencies, 10 years after radiotherapy. Gonadotroph, thyrotroph, corticotroph and somatotroph deficiencies occurred in 37, 28, 18 and 15% of patients, respectively. Hyperprolactinemia was found in 13% of patients. None patient had only one pituitary deficiency. In the multivariate analysis, a delivered dose to the PG ≥ 50 Gy or a meningioma size ≥40 mm significantly increased the risk of developing hypopituitarism.

          Conclusions

          Over a long-term follow-up, cranial radiation therapy used in skull base meningiomas led to a high prevalence of hypopituitarism, further pronounced in case of tumor ≥4 cm. These results advocate for an annual and prolonged follow-up of the pituitary functions in patients with irradiated skull base meningiomas.

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          Most cited references24

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          The recurrence of intracranial meningiomas after surgical treatment.

          D. Simpson (1957)
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            Epidemiology and etiology of meningioma

            Although most meningiomas are encapsulated and benign tumors with limited numbers of genetic aberrations, their intracranial location often leads to serious and potentially lethal consequences. They are the most frequently diagnosed primary brain tumor accounting for 33.8% of all primary brain and central nervous system tumors reported in the United States between 2002 and 2006. Inherited susceptibility to meningioma is suggested both by family history and candidate gene studies in DNA repair genes. People with certain mutations in the neurofibromatosis gene (NF2) have a very substantial increased risk for meningioma. High dose ionizing radiation exposure is an established risk factor for meningioma, and lower doses may also increase risk, but which types and doses are controversial or understudied. Because women are twice as likely as men to develop meningiomas and these tumors harbor hormone receptors, an etiologic role for hormones (both endogenous and exogenous) has been hypothesized. The extent to which immunologic factors influence meningioma etiology has been largely unexplored. Growing emphasis on brain tumor research coupled with the advent of new genetic and molecular epidemiologic tools in genetic and molecular epidemiology promise hope for advancing knowledge about the causes of intra-cranial meningioma. In this review, we highlight current knowledge about meningioma epidemiology and etiology and suggest future research directions.
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              An overview of meningiomas

              Meningiomas are the most common primary intracranial tumor. Important advances are occurring in meningioma research. These are expected to accelerate, potentially leading to impactful changes on the management of meningiomas in the near and medium term. This review will cover the histo- and molecular pathology of meningiomas, including recent 2016 updates to the WHO classification of CNS tumors. We will discuss clinical and radiographic presentation and therapeutic management. Surgery and radiotherapy, the two longstanding primary therapeutic modalities, will be discussed at length. In addition, data from prior and ongoing investigations of other treatment modalities, including systemic and targeted therapies, will be covered. This review will quickly update the reader on the contemporary management and future directions in meningiomas.
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                Author and article information

                Contributors
                perrine.raymond@hotmail.fr
                j.salleron@nancy.unicancer.fr
                Journal
                BMC Cancer
                BMC Cancer
                BMC Cancer
                BioMed Central (London )
                1471-2407
                18 December 2021
                18 December 2021
                2021
                : 21
                : 1346
                Affiliations
                [1 ]GRID grid.452436.2, ISNI 0000 0000 8775 4825, Department of radiation therapy, , Institut de Cancérologie de Lorraine, ; 6 avenue de Bourgogne, 54519 Vandoeuvre Les Nancy, France
                [2 ]GRID grid.410527.5, ISNI 0000 0004 1765 1301, Department of Endocrinology, , University hospital CHU de Nancy, ; Rue du Morvan, 54500 Vandoeuvre Les Nancy, France
                [3 ]GRID grid.5399.6, ISNI 0000 0001 2176 4817, Department of Endocrinology, Hôpital de la Conception, , Aix Marseille Univ, APHM, Inserm, MMG, ; Marseille, France
                [4 ]GRID grid.410527.5, ISNI 0000 0004 1765 1301, Department of Neurosurgery, , University hospital CHU de Nancy, ; Nancy, France
                [5 ]GRID grid.452436.2, ISNI 0000 0000 8775 4825, Department of biostatistics, , Institut de Cancérologie de Lorraine, Université de Lorraine F-54519, ; 6 avenue de Bourgogne, 54519 Vandoeuvre Les Nancy, France
                [6 ]GRID grid.452436.2, ISNI 0000 0000 8775 4825, Department of radiation therapy, , Institut de Cancérologie de Lorraine, ; 6 avenue de Bourgogne, 54519 Vandoeuvre Les Nancy, France
                Article
                9045
                10.1186/s12885-021-09045-3
                8684631
                34922472
                68535526-eb14-4194-870d-4fb92419d74c
                © The Author(s) 2021

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 16 February 2021
                : 18 November 2021
                Categories
                Research
                Custom metadata
                © The Author(s) 2021

                Oncology & Radiotherapy
                skull base meningiomas,radiation therapy,pituitary deficiencies,increase morbi-mortality

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