Literature DB >> 32449093

Predicting development of ipilimumab-induced hypophysitis: utility of T4 and TSH index but not TSH.

M S Siddiqui1, Z M Lai1, L Spain2, V Greener1, S Turajlic2, J Larkin2, D L Morganstein3,4.   

Abstract

PURPOSE: Ipilimumab, a monoclonal antibody inhibiting CLTA-4, is an established treatment in metastatic melanoma, either alone or in combination with nivolumab, and results in immune mediated adverse events, including endocrinopathy. Hypophysitis is one of the most common endocrine abnormalities. An early recognition of hypophysitis may prevent life threatening consequences of hypopituitarism; therefore, biomarkers to predict which patients will develop hypophysitis would have clinical utility. Recent studies suggested that a decline in TSH may serve as an early marker of IH. This study was aimed at assessing the utility of thyroid function tests in predicting development of hypophysitis.
METHODS: A retrospective cohort study was performed for all patients (n = 308) treated with ipilimumab either as a monotherapy or in combination with nivolumab for advanced melanoma at the Royal Marsden Hospital from 2010 to 2016. Thyroid function tests, other pituitary function tests and Pituitary MRIs were used to identify those with hypophysitis. RESULTS AND
CONCLUSIONS: Ipilimumab-induced hypophysitis (IH) was diagnosed in 25 patients (8.15%). A decline in TSH was observed in hypophysitis cohort during the first three cycles but it did not reach statistical significance (P = 0.053). A significant fall in FT4 (P < 0.001), TSH index (P < 0.001) and standardised TSH index (P < 0.001) prior to cycles 3 and 4 in hypophysitis cohort was observed. TSH is not useful in predicting development of IH. FT4, TSH index and standardised TSH index may be valuable but a high index of clinical suspicion remains paramount in early detection of hypophysitis.

Entities:  

Keywords:  Hypophysitis; Ipilimumab; Melanoma; TSH index

Year:  2020        PMID: 32449093     DOI: 10.1007/s40618-020-01297-3

Source DB:  PubMed          Journal:  J Endocrinol Invest        ISSN: 0391-4097            Impact factor:   4.256


  18 in total

1.  Nivolumab and Ipilimumab in Advanced Melanoma.

Authors:  Jedd D Wolchok; Linda Rollin; James Larkin
Journal:  N Engl J Med       Date:  2017-12-21       Impact factor: 91.245

2.  Nivolumab and ipilimumab versus ipilimumab in untreated melanoma.

Authors:  Michael A Postow; Jason Chesney; Anna C Pavlick; Caroline Robert; Kenneth Grossmann; David McDermott; Gerald P Linette; Nicolas Meyer; Jeffrey K Giguere; Sanjiv S Agarwala; Montaser Shaheen; Marc S Ernstoff; David Minor; April K Salama; Matthew Taylor; Patrick A Ott; Linda M Rollin; Christine Horak; Paul Gagnier; Jedd D Wolchok; F Stephen Hodi
Journal:  N Engl J Med       Date:  2015-04-20       Impact factor: 91.245

3.  Ipilimumab-induced hypophysitis, a single academic center experience.

Authors:  Travis Snyders; Daniel Chakos; Umang Swami; Emile Latour; Yiyi Chen; Maria Fleseriu; Mohammed Milhem; Yousef Zakharia; Roula Zahr
Journal:  Pituitary       Date:  2019-10       Impact factor: 4.107

4.  Nivolumab versus chemotherapy in patients with advanced melanoma who progressed after anti-CTLA-4 treatment (CheckMate 037): a randomised, controlled, open-label, phase 3 trial.

Authors:  Jeffrey S Weber; Sandra P D'Angelo; David Minor; F Stephen Hodi; Ralf Gutzmer; Bart Neyns; Christoph Hoeller; Nikhil I Khushalani; Wilson H Miller; Christopher D Lao; Gerald P Linette; Luc Thomas; Paul Lorigan; Kenneth F Grossmann; Jessica C Hassel; Michele Maio; Mario Sznol; Paolo A Ascierto; Peter Mohr; Bartosz Chmielowski; Alan Bryce; Inge M Svane; Jean-Jacques Grob; Angela M Krackhardt; Christine Horak; Alexandre Lambert; Arvin S Yang; James Larkin
Journal:  Lancet Oncol       Date:  2015-03-18       Impact factor: 41.316

5.  Prognostic factors in metastatic melanoma: a pooled analysis of Eastern Cooperative Oncology Group trials.

Authors:  J Manola; M Atkins; J Ibrahim; J Kirkwood
Journal:  J Clin Oncol       Date:  2000-11-15       Impact factor: 44.544

6.  Long-term follow-up of ipilimumab-induced hypophysitis, a common adverse event of the anti-CTLA-4 antibody in melanoma.

Authors:  Frédérique Albarel; Caroline Gaudy; Frédéric Castinetti; Tiphaine Carré; Isabelle Morange; Bernard Conte-Devolx; Jean-Jacques Grob; Thierry Brue
Journal:  Eur J Endocrinol       Date:  2014-11-21       Impact factor: 6.664

7.  Fall in thyroid stimulating hormone (TSH) may be an early marker of ipilimumab-induced hypophysitis.

Authors:  Sunita M C De Sousa; Nisa Sheriff; Chau H Tran; Alexander M Menzies; Venessa H M Tsang; Georgina V Long; Katherine T T Tonks
Journal:  Pituitary       Date:  2018-06       Impact factor: 4.107

8.  Ipilimumab-induced hypophysitis: a detailed longitudinal analysis in a large cohort of patients with metastatic melanoma.

Authors:  Alexander T Faje; Ryan Sullivan; Donald Lawrence; Nicholas A Tritos; Riley Fadden; Anne Klibanski; Lisa Nachtigall
Journal:  J Clin Endocrinol Metab       Date:  2014-07-31       Impact factor: 5.958

Review 9.  Current Diagnosis and Management of Immune Related Adverse Events (irAEs) Induced by Immune Checkpoint Inhibitor Therapy.

Authors:  Vivek Kumar; Neha Chaudhary; Mohit Garg; Charalampos S Floudas; Parita Soni; Abhinav B Chandra
Journal:  Front Pharmacol       Date:  2017-02-08       Impact factor: 5.810

Review 10.  Development of ipilimumab: a novel immunotherapeutic approach for the treatment of advanced melanoma.

Authors:  Jedd D Wolchok; F Stephen Hodi; Jeffrey S Weber; James P Allison; Walter J Urba; Caroline Robert; Steven J O'Day; Axel Hoos; Rachel Humphrey; David M Berman; Nils Lonberg; Alan J Korman
Journal:  Ann N Y Acad Sci       Date:  2013-06-17       Impact factor: 5.691

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  1 in total

Review 1.  Endocrine toxicity of cancer immunotherapy: clinical challenges.

Authors:  Bliss Anderson; Daniel L Morganstein
Journal:  Endocr Connect       Date:  2021-03       Impact factor: 3.335

  1 in total

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