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Inflammation-induced hypoparathyroidism triggered by combination immune checkpoint blockade for melanoma

BACKGROUND: Treatment with a combination of PD-1 and CTLA-4 targeted checkpoint inhibition has improved outcome of melanoma patients and led to durable remissions but is also associated with significant toxicities. Endocrinopathies such as thyroiditis and hypophysitis are often seen, but other, rare...

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Autores principales: Trinh, Beckey, Sanchez, Guacimara Ortega, Herzig, Petra, Läubli, Heinz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385398/
https://www.ncbi.nlm.nih.gov/pubmed/30791949
http://dx.doi.org/10.1186/s40425-019-0528-x
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author Trinh, Beckey
Sanchez, Guacimara Ortega
Herzig, Petra
Läubli, Heinz
author_facet Trinh, Beckey
Sanchez, Guacimara Ortega
Herzig, Petra
Läubli, Heinz
author_sort Trinh, Beckey
collection PubMed
description BACKGROUND: Treatment with a combination of PD-1 and CTLA-4 targeted checkpoint inhibition has improved outcome of melanoma patients and led to durable remissions but is also associated with significant toxicities. Endocrinopathies such as thyroiditis and hypophysitis are often seen, but other, rarer disturbances have also been described. Endocrinopathies affecting the parathyroid gland are rarely reported and no clear pathomechanism has been proposed. CASE PRESENTATION: Here, we report a case of severe hypocalcemia due to an antibody-mediated hypoparathyroidism as an immune-related adverse event (irAE) in a patient who was treated with the anti-PD-1 antibody nivolumab and anti-CTLA-4 antibody ipilimumab. Hypocalcemia was rapidly corrected by substitution, but the endogenous serum parathyroid hormone (PTH) remained low. The patient demonstrated a rapid and profound tumor response to the combination immune checkpoint blockade, but developed a severe colitis that required high-dose intravenous corticosteroid and anti-TNFα therapy. During this strong immunosuppression the PTH level normalized and the calcium levels were stable without substitution. However, during tapering of immunosuppressants, the PTH and calcium levels decreased again to a level requiring calcium substitution. CONCLUSION: Our report demonstrates a rare endocrinopathy as a complication of combined PD-1 and CTLA-4 blockade. In addition, it provides evidence from the course of the disease that inflammation within the parathyroid gland is involved in the mechanism.
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spelling pubmed-63853982019-03-01 Inflammation-induced hypoparathyroidism triggered by combination immune checkpoint blockade for melanoma Trinh, Beckey Sanchez, Guacimara Ortega Herzig, Petra Läubli, Heinz J Immunother Cancer Case Report BACKGROUND: Treatment with a combination of PD-1 and CTLA-4 targeted checkpoint inhibition has improved outcome of melanoma patients and led to durable remissions but is also associated with significant toxicities. Endocrinopathies such as thyroiditis and hypophysitis are often seen, but other, rarer disturbances have also been described. Endocrinopathies affecting the parathyroid gland are rarely reported and no clear pathomechanism has been proposed. CASE PRESENTATION: Here, we report a case of severe hypocalcemia due to an antibody-mediated hypoparathyroidism as an immune-related adverse event (irAE) in a patient who was treated with the anti-PD-1 antibody nivolumab and anti-CTLA-4 antibody ipilimumab. Hypocalcemia was rapidly corrected by substitution, but the endogenous serum parathyroid hormone (PTH) remained low. The patient demonstrated a rapid and profound tumor response to the combination immune checkpoint blockade, but developed a severe colitis that required high-dose intravenous corticosteroid and anti-TNFα therapy. During this strong immunosuppression the PTH level normalized and the calcium levels were stable without substitution. However, during tapering of immunosuppressants, the PTH and calcium levels decreased again to a level requiring calcium substitution. CONCLUSION: Our report demonstrates a rare endocrinopathy as a complication of combined PD-1 and CTLA-4 blockade. In addition, it provides evidence from the course of the disease that inflammation within the parathyroid gland is involved in the mechanism. BioMed Central 2019-02-21 /pmc/articles/PMC6385398/ /pubmed/30791949 http://dx.doi.org/10.1186/s40425-019-0528-x Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Trinh, Beckey
Sanchez, Guacimara Ortega
Herzig, Petra
Läubli, Heinz
Inflammation-induced hypoparathyroidism triggered by combination immune checkpoint blockade for melanoma
title Inflammation-induced hypoparathyroidism triggered by combination immune checkpoint blockade for melanoma
title_full Inflammation-induced hypoparathyroidism triggered by combination immune checkpoint blockade for melanoma
title_fullStr Inflammation-induced hypoparathyroidism triggered by combination immune checkpoint blockade for melanoma
title_full_unstemmed Inflammation-induced hypoparathyroidism triggered by combination immune checkpoint blockade for melanoma
title_short Inflammation-induced hypoparathyroidism triggered by combination immune checkpoint blockade for melanoma
title_sort inflammation-induced hypoparathyroidism triggered by combination immune checkpoint blockade for melanoma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385398/
https://www.ncbi.nlm.nih.gov/pubmed/30791949
http://dx.doi.org/10.1186/s40425-019-0528-x
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