Autoimmune hypophysitis associated with new anti-cancer immunotherapies

Jannin, Arnaud; Merlen, Emilie; Do Cao, Christine; Penel, Nicolas

Document type :

Article dans une revue scientifique: Article de synthèse/Review paper

DOI :

10.1016/j.bulcan.2017.10.033

PMID :

29475597

Permalink :

http://hdl.handle.net/20.500.12210/17290

Title :

Autoimmune hypophysitis associated with new anti-cancer immunotherapies

Author(s) :

Jannin, Arnaud [Auteur]
Merlen, Emilie [Auteur]
Do Cao, Christine [Auteur]
Penel, Nicolas [Auteur]

Evaluation des technologies de santé et des pratiques médicales - ULR 2694 [METRICS]

Journal title :

Bulletin du cancer

Abbreviated title :

Bull Cancer

Publication date :

2018-02-20

ISSN :

1769-6917

English keyword(s) :

Cancer
Immunotherapy
Hypophysitis
Diagnosis
Treatment

HAL domain(s) :

Sciences du Vivant [q-bio]

English abstract : [en]

Recently developed immunotherapeutic agents, like anti-cytotoxic T lymphocyte antigen 4 antibody (CTLA4), anti-programmed cell death 1 (PD1) or anti-programmed cell death-ligand 1 (PDL1), have demonstrated substantial ...
Show more >Recently developed immunotherapeutic agents, like anti-cytotoxic T lymphocyte antigen 4 antibody (CTLA4), anti-programmed cell death 1 (PD1) or anti-programmed cell death-ligand 1 (PDL1), have demonstrated substantial potential for the treatment of a variety of malignancies. Autoimmune side effects from these agents are diverse and can include multiple endocrinopathies like immunotherapy induced hypophysitis (IH). These toxicities appear to be more frequent in patients receiving anti-CTLA4 antibody compared to PD1/PDL1 agents. The diagnosis of IH is generally based on the presence of new hypopituitarism without an alternative etiology and radiographic pituitary enlargement or not while on treatment with Immunotherapy. Patients with IH frequently present non-specifics symptoms like headache, fatigue or weakness. ACTH and TSH deficiencies are more frequent. TSH and gonadotrophin deficiencies may be reversible but ACTH deficiency appears permanent. Glucocorticoid and thyroid hormone replacement should be instituted early after the diagnosis of IH, androgen replacement can be deferred initially and discussed by the patient. High-dose glucocorticoid does not improve the outcome of IH and should be reserved for patients with persistent severe headache, severe hyponatremia or visual defects. Patient education, early identification by measuring TSH, free thyroxine, morning ACTH and cortisol levels before each treatment cycle and proper treatment are the core of IH management.Show less >

Language :

Anglais

Audience :

Internationale

Popular science :

Non

Administrative institution(s) :

CHU Lille
Université de Lille

Collections :

METRICS : Evaluation des technologies de santé et des pratiques médicales - ULR 2694

Submission date :

2019-12-09T18:18:01Z

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