Erman Ana, Ignjatović Marija, Leskovšek Katja, Miceska Simona, Lampreht Tratar Urša, Bošnjak Maša, Kloboves Prevodnik Veronika, Čemažar Maja, Kandolf Sekulovič Lidija, Avguštin Gorazd, Ocvirk Janja, Mesti Tanja
Department of Medical Oncology, Institute of Oncology Ljubljana, Zaloška Cesta 2, 1000 Ljubljana, Slovenia.
Medical Faculty, University of Ljubljana, Kongresni Trg 12, 1000 Ljubljana, Slovenia.
Biomedicines. 2023 Jul 18;11(7):2016. doi: 10.3390/biomedicines11072016.
BACKGROUND: Immunotherapy has been successful in treating advanced melanoma, but a large proportion of patients do not respond to the treatment with immune checkpoint inhibitors (ICIs). Preclinical and small cohort studies suggest gastrointestinal microbiome composition and exosomal mRNA expression of PD-L1 and IFNγ from the primary tumor, stool and body fluids as potential biomarkers for response. METHODS: Patients treated with immune checkpoint inhibitors as a first line treatment for metastatic melanoma are recruted to this prospective study. Stool samples are submitted before the start of treatment, at the 12th (+/-2) week and 28th (+/-2) week, and at the occurrence of event (suspected disease progression/hyperprogression, immune-related adverse event (irAE), deterioration). Peripheral venous blood samples are taken additionally at the same time points for cytologic and molecular tests. Histological material from the tumor tissue is obtained before the start of immunotherapy treatment. Primary objectives are to determine whether the human gastrointestinal microbiome (bacterial and viral) and the exosomal mRNA expression of PD-L1 and IFNγ and its dynamics predicts the response to treatment with PD-1 and CTLA-4 inhibitors and its association with the occurrence of irAE. The response is evaluated radiologically with imaging methods in accordance with the irRECIST criteria. CONCLUSIONS: This is the first study to combine and investigate multiple potential predictive and prognostic biomarkers and their dynamics in first line ICI in metastatic melanoma patients.
背景:免疫疗法已成功用于治疗晚期黑色素瘤,但很大一部分患者对免疫检查点抑制剂(ICI)治疗无反应。临床前和小队列研究表明,胃肠道微生物群组成以及原发肿瘤、粪便和体液中PD-L1和IFNγ的外泌体mRNA表达可作为反应的潜在生物标志物。 方法:将接受免疫检查点抑制剂作为转移性黑色素瘤一线治疗的患者纳入这项前瞻性研究。在治疗开始前、第12(±2)周和第28(±2)周以及事件发生时(疑似疾病进展/超进展、免疫相关不良事件(irAE)、病情恶化)提交粪便样本。在相同时间点额外采集外周静脉血样本进行细胞学和分子检测。在免疫治疗开始前获取肿瘤组织的组织学材料。主要目的是确定人类胃肠道微生物群(细菌和病毒)以及PD-L1和IFNγ的外泌体mRNA表达及其动态变化是否能预测对PD-1和CTLA-4抑制剂治疗的反应及其与irAE发生的关联。根据irRECIST标准,采用影像学方法对反应进行放射学评估。 结论:这是第一项在转移性黑色素瘤患者的一线ICI治疗中,结合并研究多种潜在预测和预后生物标志物及其动态变化的研究。
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