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人类胃肠道微生物群以及程序性死亡受体配体1(PD-L1)和干扰素γ(IFNγ)的外泌体mRNA表达对转移性黑色素瘤患者免疫检查点抑制剂反应的预后和预测价值:PROTOCOL试验

The Prognostic and Predictive Value of Human Gastrointestinal Microbiome and Exosomal mRNA Expression of PD-L1 and IFNγ for Immune Checkpoint Inhibitors Response in Metastatic Melanoma Patients: PROTOCOL TRIAL.

作者信息

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

机构信息

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.

出版信息

Biomedicines. 2023 Jul 18;11(7):2016. doi: 10.3390/biomedicines11072016.


DOI:10.3390/biomedicines11072016
PMID:37509655
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10377397/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92b5/10377397/f3daf674fbdc/biomedicines-11-02016-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92b5/10377397/f3daf674fbdc/biomedicines-11-02016-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92b5/10377397/f3daf674fbdc/biomedicines-11-02016-g001.jpg

相似文献

[1]
The Prognostic and Predictive Value of Human Gastrointestinal Microbiome and Exosomal mRNA Expression of PD-L1 and IFNγ for Immune Checkpoint Inhibitors Response in Metastatic Melanoma Patients: PROTOCOL TRIAL.

Biomedicines. 2023-7-18

[2]
Biomarkers for Response of Melanoma Patients to Immune Checkpoint Inhibitors: A Systematic Review.

Front Oncol. 2017-9-27

[3]
Biomarkers for Clinical Benefit of Immune Checkpoint Inhibitor Treatment-A Review From the Melanoma Perspective and Beyond.

Front Immunol. 2018-6-28

[4]
A whole-blood RNA transcript-based gene signature is associated with the development of CTLA-4 blockade-related diarrhea in patients with advanced melanoma treated with the checkpoint inhibitor tremelimumab.

J Immunother Cancer. 2018-9-18

[5]
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[6]
The Next Immune-Checkpoint Inhibitors: PD-1/PD-L1 Blockade in Melanoma.

Clin Ther. 2015-4-1

[7]
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J Eur Acad Dermatol Venereol. 2020-5

[8]
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[9]
Conversion of unresponsiveness to immune checkpoint inhibition by fecal microbiota transplantation in patients with metastatic melanoma: study protocol for a randomized phase Ib/IIa trial.

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[10]
Clinical characteristics of gastrointestinal immune-related adverse events of immune checkpoint inhibitors and their association with survival.

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引用本文的文献

[1]
Prognostic utility of the CALLY index in metastatic melanoma: building a nomogram for Patients on Anti-PD-1 therapy.

Clin Transl Oncol. 2025-3-16

[2]
Influencing immunity: role of extracellular vesicles in tumor immune checkpoint dynamics.

Exp Mol Med. 2024-11

[3]
Role of circular RNAs and gut microbiome in gastrointestinal cancers and therapeutic targets.

Noncoding RNA Res. 2023-12-15

本文引用的文献

[1]
Biomarkers for Outcome in Metastatic Melanoma in First Line Treatment with Immune Checkpoint Inhibitors.

Biomedicines. 2023-3-1

[2]
Modeling the effect of gut microbiome on therapeutic efficacy of immune checkpoint inhibitors against cancer.

Math Biosci. 2022-8

[3]
Prognostic significance of programmed cell death-ligand 1 expression on circulating tumor cells in various cancers: A systematic review and meta-analysis.

Cancer Med. 2021-10

[4]
Changes in expression of PD-L1 on peripheral T cells in patients with melanoma and lung cancer treated with PD-1 inhibitors.

Sci Rep. 2021-7-28

[5]
Interferon-γ: teammate or opponent in the tumour microenvironment?

Nat Rev Immunol. 2022-3

[6]
Adverse events during immunotherapy in Slovenian patients with metastatic melanoma reveal a positive correlation with better treatment outcomes.

Radiol Oncol. 2021-5-4

[7]
A review on the role of gut microbiota in immune checkpoint blockade therapy for cancer.

Mamm Genome. 2021-8

[8]
Exosomal PD-L1: New Insights Into Tumor Immune Escape Mechanisms and Therapeutic Strategies.

Front Cell Dev Biol. 2020-10-15

[9]
Quantifying PD-L1 Expression to Monitor Immune Checkpoint Therapy: Opportunities and Challenges.

Cancers (Basel). 2020-10-29

[10]
Impact of the Microbiome on the Immune System.

Crit Rev Immunol. 2019

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