Association of Systemic Steroid Treatment and Outcome in Patients Treated with Immune Checkpoint Inhibitors: A Real-World Analysis

Background: Immune-related adverse events (irAEs) are inflammatory side effects, which can occur during immune-checkpoint(s) inhibitors (ICIs) therapy. Steroids are the first-line agents to manage irAEs because of their immunosuppressive properties. However, it is still debated whether or when stero...

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Published inMolecules (Basel, Switzerland) Vol. 26; no. 19; p. 5789
Main Authors Paderi, Agnese, Gambale, Elisabetta, Botteri, Cristina, Giorgione, Roberta, Lavacchi, Daniele, Brugia, Marco, Mazzoni, Francesca, Giommoni, Elisa, Bormioli, Susanna, Amedei, Amedeo, Pillozzi, Serena, Matucci Cerinic, Marco, Antonuzzo, Lorenzo
Format Journal Article
LanguageEnglish
Published Basel MDPI AG 24.09.2021
MDPI
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Summary:Background: Immune-related adverse events (irAEs) are inflammatory side effects, which can occur during immune-checkpoint(s) inhibitors (ICIs) therapy. Steroids are the first-line agents to manage irAEs because of their immunosuppressive properties. However, it is still debated whether or when steroids can be administered without abrogating the therapeutic efforts of immunotherapy. Methods: We retrospectively evaluated 146 patients with metastatic non-small cell lung cancer (NSCLC), melanoma and renal cell carcinoma (RCC) treated with ICIs. We assessed the progression-free survival (PFS) of patients treated with steroids due to an irAE compared to a no-steroid group. Results: The early treatment with steroid (within the first 30 days from the beginning of immunotherapy) was not related to a shorter PFS (p = 0.077). Interestingly, patients who were treated with steroids after 30 days from the start of immunotherapy had significantly longer PFS (p = 0.017). In a multivariate analysis, treatment with steroids after 30 days was an independent prognostic factor for PFS (HR: 0.59 [95% CI 0.36–0.97], p = 0.037). Conclusions: This retrospective study points out that early systemic steroids administration to manage irAEs might not have a detrimental effect on patient clinical outcome in NSCLC, melanoma and RCC patients.
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ISSN:1420-3049
1420-3049
DOI:10.3390/molecules26195789