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      Immune check point inhibitors-induced hypophysitis: a retrospective analysis of the French Pharmacovigilance database

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          Abstract

          Immune control point (ICI) inhibitors represent a significant advance in the management and survival of cancers such as melanoma or non-small cell bronchial carcinoma. However, they induce unusual side effects, such as hypophysitis, which are rarely described elsewhere. This nationwide retrospective study describes the characteristics of hypophysitis reported in the French pharmacovigilance database (FPVD). We requested for all cases of ICI-related hypophysitis registered in the FPVD before May 2018. An endocrinologist and a pharmacologist reviewed all cases. About 94 pituitary cases were selected, involving 49 females and 45 men. Ipilimumab alone or in combination was the most represented ICI (56%). Most cases (61%) were grade 3 severity and the majority (90%) were corticotropic deficiency cases. Cases with thyroid and/or gonadotropic involvement were 21% and 1% respectively. Five patients (8%) had panhypopituitarism. Pituitary MRI, when performed, was in favor of hypophysitis in 50%. No patient recovered his previous hormonal function. The mean time of onset was significantly shorter with ipilimumab than other ICIs. ICI-related hypophysitis generate deficits that do not spontaneously recover, even at a distance from the event, unlike thyroiditis. Patients must then benefit from long-term coordinated onco-endocrinological management, adapted to their own specific deficits.

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          Immune-related adverse events for anti-PD-1 and anti-PD-L1 drugs: systematic review and meta-analysis

          To evaluate rates of serious organ specific immune-related adverse events, general adverse events related to immune activation, and adverse events consistent with musculoskeletal problems for anti-programmed cell death 1 (PD-1) drugs overall and compared with control treatments.
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            Immune Checkpoint Inhibitors: Review and Management of Endocrine Adverse Events.

            : In recent years, immune checkpoint inhibitors have emerged as effective therapies for advanced neoplasias. As new checkpoint target blockers become available and additional tumor locations tested, their use is expected to increase within a short time. Immune-related adverse events (irAEs) affecting the endocrine system are among the most frequent and complex toxicities. Some may be life-threatening if not recognized; hence, appropriate guidance for oncologists is needed. Despite their high incidence, endocrine irAEs have not been fully described for all immunotherapy agents available. This article is a narrative review of endocrinopathies associated with cytotoxic T lymphocyte-associated antigen-4, blockade of programmed death receptor 1 and its ligand inhibitors, and their combination. Thyroid dysfunction is the most frequent irAE reported, and hypophysitis is characteristic of ipilimumab. Incidence, timing patterns, and clinical presentation are discussed, and practical recommendations for clinical management are suggested. Heterogeneous terminology and lack of appropriate resolution criteria in clinical trials make adequate evaluation of endocrine AEs difficult. It is necessary to standardize definitions to contrast incidences and characterize toxicity patterns. To provide optimal care, a multidisciplinary team that includes endocrinology specialists is recommended.
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              MECHANISMS IN ENDOCRINOLOGY: Hypophysitis: diagnosis and treatment

              Hypophysitis is a rare condition characterised by inflammation of the pituitary gland, usually resulting in hypopituitarism and pituitary enlargement. Pituitary inflammation can occur as a primary hypophysitis (most commonly lymphocytic, granulomatous or xanthomatous disease) or as secondary hypophysitis (as a result of systemic diseases, immunotherapy or alternative sella-based pathologies). Hypophysitis can be classified using anatomical, histopathological and aetiological criteria. Non-invasive diagnosis of hypophysitis remains elusive, and the use of currently available serum anti-pituitary antibodies are limited by low sensitivity and specificity. Newer serum markers such as anti-rabphilin 3A are yet to show consistent diagnostic value and are not yet commercially available. Traditionally considered a very rare condition, the recent recognition of IgG4-related disease and hypophysitis as a consequence of use of immune modulatory therapy has resulted in increased understanding of the pathophysiology of hypophysitis. Modern imaging techniques, histological classification and immune profiling are improving the accuracy of the diagnosis of the patient with hypophysitis. The objective of this review is to bring readers up-to-date with current understanding of conditions presenting as hypophysitis, focussing on recent advances and areas for future development. We describe the presenting features, investigation and diagnostic approach of the patient with likely hypophysitis, including existing conventional techniques and those in the research/development arena. Hypophysitis usually results in acute and persistent pituitary hormone deficiency requiring long-term replacement. Management of hypophysitis includes control of the inflammatory pituitary mass using a variety of treatment strategies including surgery and medical therapy. Glucocorticoids remain the mainstay of medical treatment but other immunosuppressive agents (e.g. azathioprine, rituximab) show benefit in some cases, but there is a need for controlled studies to inform practice.
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                Author and article information

                Contributors
                pierre.gillet@univ-lorraine.fr
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                19 December 2019
                19 December 2019
                2019
                : 9
                : 19419
                Affiliations
                [1 ]ISNI 0000 0004 1765 1301, GRID grid.410527.5, Department of Clinical Pharmacology and Pharmacovigilance, , University Hospital of Nancy Brabois, Biologie Médicale & Biopathologie, ; Rue du Morvan, 54511 Vandoeuvre Lès Nancy, France
                [2 ]ISNI 0000 0004 1765 1301, GRID grid.410527.5, Department of Endocrinology and Medical Gynecology, , University Hospital of Nancy, rue du Morvan, ; 54500 Vandœuvre-lès-Nancy, France
                [3 ]ISNI 0000 0004 1758 9034, GRID grid.463896.6, UMR 7365 CNRS-Université de Lorraine, IMoPA, Campus Brabois Santé, 9 Avenue de la forêt de Haye, BP 20199, ; 54505 Vandœuvre-lès-Nancy, France
                [4 ]ISNI 0000 0001 0407 1584, GRID grid.414336.7, Department of Clinical Pharmacology and Pharmacovigilance, , University Hospital of Marseille, ; 270 Boulevard Sainte Marguerite, 13009 Marseille, France
                [5 ]ISNI 0000 0004 0472 0160, GRID grid.411149.8, Department of Pharmacology, , University Hospital of Caen, Avenue de la Côte de Nacre, ; 14000 Caen, France
                [6 ]ISNI 0000 0001 2292 1474, GRID grid.412116.1, Department of Pharmacovigilance, Hôpital Henri Mondor, Assistance Publique Hôpitaux de Paris, , Henri Mondor Hospital, ; 94010 Créteil, France
                Author information
                http://orcid.org/0000-0002-0598-7508
                Article
                56026
                10.1038/s41598-019-56026-5
                6923385
                31857638
                33b37f6e-e069-43a7-9c2d-5ae12804bd7a
                © The Author(s) 2019

                Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 17 July 2019
                : 30 November 2019
                Funding
                Funded by: GW consulted for Novartis and Theramex and received punctual compensations.
                Categories
                Article
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                © The Author(s) 2019

                Uncategorized
                cancer immunotherapy,multihormonal system disorders
                Uncategorized
                cancer immunotherapy, multihormonal system disorders

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