Please use this identifier to cite or link to this item: https://hdl.handle.net/1/1580
Title: Ipilimumab-induced hypophysitis in melanoma patients: an Australian case series
Authors: Chan, Matthew M K ;Lam, T.;Sweeting, A.N.;De Sousa, S.M.;Clements, A.;Carlino, M.S.;Long, G.V.;Tonks, K.T.;Chua, E.;Kefford, R.F.;Chipps, D.R.
Issue Date: Oct-2015
Source: Volume 45, Issue 10, pp. 1066 - 1073
Journal title: Internal Medicine Journal
Abstract: BACKGROUND: Ipilimumab (Yervoy; Bristol-Myers Squibb) is a novel fully humanised monoclonal antibody that blocks cytotoxic T-lymphocyte antigen 4, an immune checkpoint molecule, to augment anti-tumour T-cell responses. It is associated with significant immune-related side-effects including hypophysitis. AIM: We reviewed the clinical and biochemical characteristics of 10 patients with ipilimumab-induced hypophysitis (IH), and developed guidelines for the early detection and management of IH based on our experiences at three major teaching hospitals in Sydney. METHODS: All patients were evaluated at the Crown Princess Mary Cancer Centre and Department of Endocrinology, Westmead Hospital, Department of Endocrinology, Royal Prince Alfred Hospital, the Melanoma Institute Australia and Macarthur Cancer Therapy Centre, Campbelltown Hospital from 2010 to 2014. Relevant data were extracted by review of medical records. Main outcome measures included clinical features, hormone profile and radiological findings associated with IH, and presence of pituitary recovery. RESULTS: Ten patients were identified with IH. In four patients who underwent monitoring of plasma cortisol, there was a fall in levels in the weeks prior to presentation. The pituitary-adrenal and pituitary-thyroid axes were affected in the majority of patients, with the need for physiological hormone replacement. Imaging abnormalities were identified in five of 10 patients, and resolved without high-dose glucocorticoid therapy. To date, all patients remain on levothyroxine and hydrocortisone replacement, where appropriate. CONCLUSIONS: There is significant morbidity associated with development of IH. We suggest guidelines to assist with early recognition and therapeutic intervention.
URI: https://elibrary.cclhd.health.nsw.gov.au/cclhdjspui/handle/1/1580
DOI: 10.1111/imj.12819
Pubmed: https://www.ncbi.nlm.nih.gov/pubmed/26010858
ISSN: 1444-0903
Publicaton type: Journal Article
Keywords: Cancer
Drug Therapy
Study or Trial: Multicentre Studies
Appears in Collections:Oncology / Cancer

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