Suppr超能文献

新辅助免疫治疗:一种有前途的新标准治疗。

Neoadjuvant Immunotherapy: A Promising New Standard of Care.

机构信息

University Hospital of Geneva, 1205 Geneva, Switzerland.

University Hospital of Lausanne, 1005 Lausanne, Switzerland.

出版信息

Int J Mol Sci. 2023 Jul 24;24(14):11849. doi: 10.3390/ijms241411849.

Abstract

Neoadjuvant immunotherapy has emerged as a promising approach in the treatment of various malignancies, with preclinical studies showing improved immune responses in the preoperative setting. FDA-approved neoadjuvant-immunotherapy-based approaches include triple-negative breast cancer and early non-small cell lung cancer on the basis of improvement in pathological response and event free survival. Nevertheless, current trials have only shown benefits in a fraction of patients. It is therefore crucial to identify predictive biomarkers to improve patient selection for such approaches. This review aims to provide an overview of potential biomarkers of neoadjuvant immunotherapy in early triple-negative breast cancer, bladder cancer, melanoma, non-small cell lung cancer, colorectal cancer and gastric cancer. By the extrapolation of the metastatic setting, we explore known predictive biomarkers, i.e., PD-L1, mismatch repair deficiency and tumour mutational burden, as well as potential early-disease-specific biomarkers. We also discuss the challenges of identifying reliable biomarkers and the need for standardized protocols and guidelines for their validation and clinical implementation.

摘要

新辅助免疫疗法在治疗各种恶性肿瘤方面已经崭露头角,临床前研究表明术前新辅助免疫疗法可改善免疫反应。美国食品药品监督管理局(FDA)批准的新辅助免疫疗法包括三阴性乳腺癌和早期非小细胞肺癌,其疗效基于病理缓解和无事件生存期的改善。然而,目前的临床试验仅显示了对一部分患者的益处。因此,确定预测生物标志物以改善此类方法的患者选择至关重要。本综述旨在概述早期三阴性乳腺癌、膀胱癌、黑色素瘤、非小细胞肺癌、结直肠癌和胃癌新辅助免疫治疗的潜在生物标志物。通过对转移性疾病的推断,我们探讨了已知的预测生物标志物,即 PD-L1、错配修复缺陷和肿瘤突变负担,以及潜在的早期疾病特异性生物标志物。我们还讨论了确定可靠生物标志物的挑战以及对其进行验证和临床实施的标准化方案和指南的需求。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7ef/10380420/cf343e5d6e74/ijms-24-11849-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验