Abstract B154: Differential effects of corticosteroids and anti-TNF on tumor-specific immune responses— Implications for the management of irAEs

M. Donia, T. H. Borch, H. D. Radic, C. Chamberlain, A. Gokuldass, I. Svane, A. Draghi
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Abstract

Background: Up to 60% of patients treated with cancer immunotherapy develop severe or life threatening immune-related adverse events (irAEs). Immunosuppression with high doses of corticosteroids or, in refractory cases, with tumor necrosis factor (TNF) antagonists, are the mainstay of treatment for irAEs. It is currently unknown what is the impact of corticosteroids and anti-TNF on the activity of antitumor T-cells. Methods: The influence of clinically relevant doses of dexamethasone (corresponding to an oral dose of 10 to 125 mg prednisolone) and infliximab (anti-TNF) on the activation and killing capacity of tumor-infiltrating lymphocytes (TILs) was tested in vitro. Results: Overall, dexamethasone at low or intermediate/high dose impaired the activation (respectively -46% and -62% in n=8) and tumor-killing ability (respectively -48% and -53% in n=6) of tumor-specific TILs. In contrast, a standard clinical dose of infliximab only had a minor effect on T-cell activation and tumor killing (respectively -20% in n=8 and -10% in n=6). A brief resting following exposure to dexamethasone was sufficient to rescue the in vitro activity of TILs. Conclusions: Clinically relevant doses of infliximab only influenced to a lesser extent the activity of tumor-specific TILs in vitro, whereas even low doses of corticosteroids markedly impaired the antitumor activity of TILs. These data support steroid-sparing strategies and early initiation of anti-TNF for the treatment of irAEs in immuno-oncology. Citation Format: Marco Donia, Troels H. Borch, Haja D. Radic, Christopher Chamberlain, Aishwarya Gokuldass, Inge Marie Stentoft Svane, Arianna Draghi. Differential effects of corticosteroids and anti-TNF on tumor-specific immune responses— Implications for the management of irAEs [abstract]. In: Proceedings of the Fourth CRI-CIMT-EATI-AACR International Cancer Immunotherapy Conference: Translating Science into Survival; Sept 30-Oct 3, 2018; New York, NY. Philadelphia (PA): AACR; Cancer Immunol Res 2019;7(2 Suppl):Abstract nr B154.
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摘要:糖皮质激素和抗肿瘤坏死因子对肿瘤特异性免疫反应的不同影响-对irAEs管理的影响
背景:高达60%的接受癌症免疫治疗的患者发生严重或危及生命的免疫相关不良事件(irAEs)。高剂量皮质类固醇的免疫抑制或在难治性病例中使用肿瘤坏死因子(TNF)拮抗剂是治疗irAEs的主要方法。目前尚不清楚皮质类固醇和抗肿瘤坏死因子对抗肿瘤t细胞活性的影响。方法:采用体外实验方法,检测临床相关剂量地塞米松(相当于口服10 ~ 125 mg强的松龙)和英夫利昔单抗(抗肿瘤坏死因子)对肿瘤浸润淋巴细胞(til)激活和杀伤能力的影响。结果:总体而言,低剂量或中/高剂量地塞米松使肿瘤特异性til的激活(n=8分别为-46%和-62%)和肿瘤杀伤能力(n=6分别为-48%和-53%)受损。相比之下,标准临床剂量的英夫利昔单抗仅对t细胞活化和肿瘤杀伤有轻微影响(n=8时分别为-20%和n=6时分别为-10%)。暴露于地塞米松后的短暂休息足以恢复TILs的体外活性。结论:临床相关剂量的英夫利昔单抗仅在较小程度上影响肿瘤特异性TILs的体外活性,而即使是低剂量的皮质类固醇也会显著损害TILs的抗肿瘤活性。这些数据支持类固醇节约策略和抗肿瘤坏死因子早期启动治疗免疫肿瘤学中的irae。引用格式:Marco Donia, Troels H. Borch, Haja D. Radic, Christopher Chamberlain, Aishwarya Gokuldass, Inge Marie Stentoft Svane, Arianna Draghi。皮质类固醇和抗肿瘤坏死因子对肿瘤特异性免疫反应的不同影响-对irAEs管理的影响[摘要]。第四届CRI-CIMT-EATI-AACR国际癌症免疫治疗会议:将科学转化为生存;2018年9月30日至10月3日;纽约,纽约。费城(PA): AACR;癌症免疫学杂志,2019;7(2增刊):摘要nr B154。
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