Abstract

Simple SummaryThe aim of this study is to search for APA and AHA and related pituitary dysfunction in patients treated with immunotherapy. APA and AHA could represent markers for early detection of patients at risk of developing pituitary deficiencies related to immune checkpoint inhibitors and undergoing closer follow-up. Furthermore, this study aims to evaluate the correlation between the presence of AHA and APA and the clinical response to checkpoint inhibitor therapy. However, further prospective studies will be needed to confirm our results.Background: Autoimmune hypophysitis is a frequent immune-related adverse event (irAE) in cancer patients treated with immunecheckpoint inhibitors. Studies seeking anti-pituitary (APA) and anti-hypothalamus (AHA) antibodies in patients treated with anti-PD-1 and anti-PD-L1 are scarce. The aim of this study is to search for APA and AHA and related pituitary dysfunction in patients treated with these agents. Methods:Cross-sectional and preliminary longitudinal studies were conducted at the Medical Oncology Unit and Endocrinology and Metabolic Diseases Unit of the University of Campania “Luigi Vanvitelli”. Fifty-four cancer patients on treatments with anti-PD-1 or anti-PD-L1 (Group 1) and 50 healthy controls were enrolled for a cross-sectional study; 13 cancer patients (Group 2) were enrolled for our preliminary longitudinal study. APA/AHA titers and changes in biochemical and hormonal profile were evaluated in Group 1; in Group 2, they were evaluated before and after nine weeks from the start of immunotherapy. Results: Patients of Group 1 showed a higher prevalence of APA and AHA than controls: 21 of them had APA, 16 had AHA, and 11 had both autoantibodies. In total, 7 of 13 patients in Group 2 became APA-positive and 3 became AHA-positive after nine weeks of immunotherapy, showing an increase in prolactin and a decrease in ACTH and IGF-1 levels compared with basal values. Conclusions:Anti-pituitary and anti-hypothalamus antibodies seem to play a pivotal role in hypothalamic–pituitary autoimmunity and secondary endocrine-related alterations evoked by anti-PD-1 and PD-L1 antibodies.

Highlights

  • Immune checkpoint inhibitors (ICIs) have been recently introduced as an effective and innovative therapy for the treatment of advanced cancer

  • Among these, an immune-targeted cancer therapy-related hypophysitis has been recognized as an endocrine immune-related adverse event (irAE) with a higher prevalence in patients treated with anti-CTLA-4 with respect to those treated with anti-PD and anti-PD-L1 agents [7,8,9,10,11,18]

  • Since APA and anti-hypothalamus (AHA) antibodies have been detected in patients with autoimmune hypophysitis, suggesting that an immune hypothalamic involvement may contribute to pituitary dysfunction [20,21], we investigated the possible occurrence of APA and AHA and related pituitary and satellite gland dysfunctions in patients treated with these agents

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Summary

Introduction

Immune checkpoint inhibitors (ICIs) have been recently introduced as an effective and innovative therapy for the treatment of advanced cancer. Among these, an immune-targeted cancer therapy-related hypophysitis has been recognized as an endocrine irAE with a higher prevalence in patients treated with anti-CTLA-4 with respect to those treated with anti-PD and anti-PD-L1 agents [7,8,9,10,11,18]. Studies investigating the occurrence of hypothalamic–pituitary autoimmunity in patients treated with PD-1 and PD-L1 inhibitors are scarce, and only anti-pituitary antibodies (APA) were detected in affected patients [19]. Since APA and anti-hypothalamus (AHA) antibodies have been detected in patients with autoimmune hypophysitis, suggesting that an immune hypothalamic involvement may contribute to pituitary dysfunction [20,21], we investigated the possible occurrence of APA and AHA and related pituitary and satellite gland dysfunctions in patients treated with these agents. Conclusions:Anti-pituitary and anti-hypothalamus antibodies seem to play a pivotal role in hypothalamic–pituitary autoimmunity and secondary endocrine-related alterations evoked by anti-PD-1 and PD-L1 antibodies

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