Immune checkpoint inhibitor therapy for ACTH-secreting pituitary carcinoma: a new emerging treatment?


Journal

European journal of endocrinology
ISSN: 1479-683X
Titre abrégé: Eur J Endocrinol
Pays: England
ID NLM: 9423848

Informations de publication

Date de publication:
Jan 2021
Historique:
received: 02 03 2020
accepted: 05 10 2020
pubmed: 29 10 2020
medline: 1 12 2020
entrez: 28 10 2020
Statut: ppublish

Résumé

Pituitary carcinomas are rare but aggressive and require maximally coordinated multimodal therapies. For refractory tumors, unresponsive to temozolomide (TMZ), therapeutic options are limited. Immune checkpoint inhibitors (ICI) may be considered for treatment as illustrated in the present case report. We report a patient with ACTH-secreting pituitary carcinoma, progressive after multiple lines of therapy including chemotherapy with TMZ, who demonstrated disease stabilization by a combination of ipilimumab (anti-CTLA-4) and nivolumab (anti-PD-1) ICI therapy. Management of pituitary carcinoma beyond TMZ remains ill-defined and relies on case reports. TMZ creates, due to hypermutation, more immunogenic tumors and subsequently potential candidates for ICI therapy. This case report adds support to the possible role of ICI in the treatment of pituitary carcinoma. ICI therapy could be a promising treatment option for pituitary carcinoma, considering the mechanisms of TMZ-induced hypermutation with increased immunogenicity, pituitary expression of CTLA-4 and PD-L1, and the frequent occurrence of hypophysitis as a side effect of ICI therapy.

Sections du résumé

BACKGROUND BACKGROUND
Pituitary carcinomas are rare but aggressive and require maximally coordinated multimodal therapies. For refractory tumors, unresponsive to temozolomide (TMZ), therapeutic options are limited. Immune checkpoint inhibitors (ICI) may be considered for treatment as illustrated in the present case report.
CASE METHODS
We report a patient with ACTH-secreting pituitary carcinoma, progressive after multiple lines of therapy including chemotherapy with TMZ, who demonstrated disease stabilization by a combination of ipilimumab (anti-CTLA-4) and nivolumab (anti-PD-1) ICI therapy.
DISCUSSION CONCLUSIONS
Management of pituitary carcinoma beyond TMZ remains ill-defined and relies on case reports. TMZ creates, due to hypermutation, more immunogenic tumors and subsequently potential candidates for ICI therapy. This case report adds support to the possible role of ICI in the treatment of pituitary carcinoma.
CONCLUSION CONCLUSIONS
ICI therapy could be a promising treatment option for pituitary carcinoma, considering the mechanisms of TMZ-induced hypermutation with increased immunogenicity, pituitary expression of CTLA-4 and PD-L1, and the frequent occurrence of hypophysitis as a side effect of ICI therapy.

Identifiants

pubmed: 33112279
doi: 10.1530/EJE-20-0151
pii: EJE-20-0151
pmc: PMC7707801
doi:
pii:

Substances chimiques

Antineoplastic Agents, Immunological 0
Ipilimumab 0
Nivolumab 31YO63LBSN

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

K1-K5

Références

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pubmed: 28766057
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pubmed: 11883868
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pubmed: 20668020
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Auteurs

Bastiaan Sol (B)

Department of Endocrinology, UZ Brussel, Laarbeeklaan, Brussels, Belgium.

Jeroen M K de Filette (JMK)

Department of Endocrinology, UZ Brussel, Laarbeeklaan, Brussels, Belgium.

Gil Awada (G)

Department of Medical Oncology, UZ Brussel, Laarbeeklaan, Brussels, Belgium.

Steven Raeymaeckers (S)

Department of Radiology, UZ Brussel, Laarbeeklaan, Brussels, Belgium.

Sandrine Aspeslagh (S)

Department of Medical Oncology, UZ Brussel, Laarbeeklaan, Brussels, Belgium.

C E Andreescu (CE)

Department of Endocrinology, UZ Brussel, Laarbeeklaan, Brussels, Belgium.

Bart Neyns (B)

Department of Medical Oncology, UZ Brussel, Laarbeeklaan, Brussels, Belgium.

Brigitte Velkeniers (B)

Department of Endocrinology, UZ Brussel, Laarbeeklaan, Brussels, Belgium.

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Classifications MeSH