Cargando…

Potential pitfalls in diagnosis of immunotherapy-induced hypothalamic–pituitary–adrenal axis abnormalities: a clinical case

SUMMARY: Short synacthen tests (SST) are frequently used for assessing adrenocorticotropin hormone (ACTH) deficiency. In this study, we present the case of a 53-year-old man receiving immunotherapy for metastatic melanoma, who subsequently developed immune checkpoint inhibitor (ICI)-induced hypothyr...

Descripción completa

Detalles Bibliográficos
Autores principales: Bi, Yixi, Adam, Safwaan, Chatzimavridou, Viktoria, Lorigan, Paul, Huang, Yinglai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10259291/
https://www.ncbi.nlm.nih.gov/pubmed/37435468
http://dx.doi.org/10.1530/EO-21-0023
_version_ 1785057628774203392
author Bi, Yixi
Adam, Safwaan
Chatzimavridou, Viktoria
Lorigan, Paul
Huang, Yinglai
author_facet Bi, Yixi
Adam, Safwaan
Chatzimavridou, Viktoria
Lorigan, Paul
Huang, Yinglai
author_sort Bi, Yixi
collection PubMed
description SUMMARY: Short synacthen tests (SST) are frequently used for assessing adrenocorticotropin hormone (ACTH) deficiency. In this study, we present the case of a 53-year-old man receiving immunotherapy for metastatic melanoma, who subsequently developed immune checkpoint inhibitor (ICI)-induced hypothyroidism and was investigated for the presence of ICI-induced hypocortisolaemia on different occasions. Despite two reassuring SSTs, he subsequently developed clinical and biochemical evidence of ACTH deficiency. The ACTH on local measurement was not conclusive in keeping with ICI-related ACTH deficiency but when repeated using an alternative assay confirmed the diagnosis. The case illustrates the evolution of ACTH deficiency and exposes the potential pitfalls of screening strategies. Two important lessons may be gleaned from this case: (i) SSTs can be normal in early cases of secondary adrenal insufficiency, for example, hypophysitis due to adrenal reserve and (ii) when there is mismatch between the clinical and biochemical presentation, the ACTH should be repeated using a different assay. LEARNING POINTS: Short synacthen tests, useful for ruling out adrenalitis and primary adrenal failure, may be normal in early adrenocorticotrophic hormone deficiency and secondary adrenal failure due to residual adrenal reserve. If clinical suspicion of adrenal insufficiency persists despite an initial satisfactory SST, it is important to recognise the need for re-assessment of cortisol levels. Insulin tolerance test remains a useful tool in the investigation of secondary adrenal insufficiency. Levothyroxine replacement may accelerate the metabolism of cortisol in cases of concurrent hypothyroidism and hypoadrenalism, and therefore, glucocorticoid replacement must precede levothyroxine treatment, to avoid adrenal crisis. The prevalence of immunotherapy-related endocrinopathies is likely to increase with increasing use of ICI and it is crucial that clinicians are alert to their subtle symptoms.
format Online
Article
Text
id pubmed-10259291
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Bioscientifica Ltd
record_format MEDLINE/PubMed
spelling pubmed-102592912023-07-11 Potential pitfalls in diagnosis of immunotherapy-induced hypothalamic–pituitary–adrenal axis abnormalities: a clinical case Bi, Yixi Adam, Safwaan Chatzimavridou, Viktoria Lorigan, Paul Huang, Yinglai Endocr Oncol Case Report SUMMARY: Short synacthen tests (SST) are frequently used for assessing adrenocorticotropin hormone (ACTH) deficiency. In this study, we present the case of a 53-year-old man receiving immunotherapy for metastatic melanoma, who subsequently developed immune checkpoint inhibitor (ICI)-induced hypothyroidism and was investigated for the presence of ICI-induced hypocortisolaemia on different occasions. Despite two reassuring SSTs, he subsequently developed clinical and biochemical evidence of ACTH deficiency. The ACTH on local measurement was not conclusive in keeping with ICI-related ACTH deficiency but when repeated using an alternative assay confirmed the diagnosis. The case illustrates the evolution of ACTH deficiency and exposes the potential pitfalls of screening strategies. Two important lessons may be gleaned from this case: (i) SSTs can be normal in early cases of secondary adrenal insufficiency, for example, hypophysitis due to adrenal reserve and (ii) when there is mismatch between the clinical and biochemical presentation, the ACTH should be repeated using a different assay. LEARNING POINTS: Short synacthen tests, useful for ruling out adrenalitis and primary adrenal failure, may be normal in early adrenocorticotrophic hormone deficiency and secondary adrenal failure due to residual adrenal reserve. If clinical suspicion of adrenal insufficiency persists despite an initial satisfactory SST, it is important to recognise the need for re-assessment of cortisol levels. Insulin tolerance test remains a useful tool in the investigation of secondary adrenal insufficiency. Levothyroxine replacement may accelerate the metabolism of cortisol in cases of concurrent hypothyroidism and hypoadrenalism, and therefore, glucocorticoid replacement must precede levothyroxine treatment, to avoid adrenal crisis. The prevalence of immunotherapy-related endocrinopathies is likely to increase with increasing use of ICI and it is crucial that clinicians are alert to their subtle symptoms. Bioscientifica Ltd 2022-06-28 /pmc/articles/PMC10259291/ /pubmed/37435468 http://dx.doi.org/10.1530/EO-21-0023 Text en © The authors https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License. (https://creativecommons.org/licenses/by/4.0/)
spellingShingle Case Report
Bi, Yixi
Adam, Safwaan
Chatzimavridou, Viktoria
Lorigan, Paul
Huang, Yinglai
Potential pitfalls in diagnosis of immunotherapy-induced hypothalamic–pituitary–adrenal axis abnormalities: a clinical case
title Potential pitfalls in diagnosis of immunotherapy-induced hypothalamic–pituitary–adrenal axis abnormalities: a clinical case
title_full Potential pitfalls in diagnosis of immunotherapy-induced hypothalamic–pituitary–adrenal axis abnormalities: a clinical case
title_fullStr Potential pitfalls in diagnosis of immunotherapy-induced hypothalamic–pituitary–adrenal axis abnormalities: a clinical case
title_full_unstemmed Potential pitfalls in diagnosis of immunotherapy-induced hypothalamic–pituitary–adrenal axis abnormalities: a clinical case
title_short Potential pitfalls in diagnosis of immunotherapy-induced hypothalamic–pituitary–adrenal axis abnormalities: a clinical case
title_sort potential pitfalls in diagnosis of immunotherapy-induced hypothalamic–pituitary–adrenal axis abnormalities: a clinical case
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10259291/
https://www.ncbi.nlm.nih.gov/pubmed/37435468
http://dx.doi.org/10.1530/EO-21-0023
work_keys_str_mv AT biyixi potentialpitfallsindiagnosisofimmunotherapyinducedhypothalamicpituitaryadrenalaxisabnormalitiesaclinicalcase
AT adamsafwaan potentialpitfallsindiagnosisofimmunotherapyinducedhypothalamicpituitaryadrenalaxisabnormalitiesaclinicalcase
AT chatzimavridouviktoria potentialpitfallsindiagnosisofimmunotherapyinducedhypothalamicpituitaryadrenalaxisabnormalitiesaclinicalcase
AT loriganpaul potentialpitfallsindiagnosisofimmunotherapyinducedhypothalamicpituitaryadrenalaxisabnormalitiesaclinicalcase
AT huangyinglai potentialpitfallsindiagnosisofimmunotherapyinducedhypothalamicpituitaryadrenalaxisabnormalitiesaclinicalcase