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非小细胞肺癌中的细胞疗法:介于神话与现实之间

Cellular Therapy in NSCLC: Between Myth and Reality.

作者信息

Imbimbo Martina, Wetterwald Laureline, Friedlaender Alex, Parikh Kaushal, Addeo Alfredo

机构信息

Oncology Department, Centre Hospitalier Universitaire Vaudois (CHUV), Rue du Bugnon 46, Lausanne University Hospital, Lausanne, Switzerland.

Oncology Department, University Hospital Geneva (HUG), 1205, Geneva, Switzerland.

出版信息

Curr Oncol Rep. 2023 Oct;25(10):1161-1174. doi: 10.1007/s11912-023-01443-z. Epub 2023 Aug 30.

Abstract

PURPOSE OF REVIEW

In this paper, we review the current state and modalities of adoptive cell therapies (ACT) in non-small cell lung carcinoma (NSCLC). We also discuss the challenges hampering the use of ACT and the approaches to overcome these barriers.

RECENT FINDINGS

Several trials are ongoing investigating the three main modalities of T cell-based ACT: tumor-infiltrating lymphocytes (TILs), genetically engineered T-cell receptors (TCRs), and chimeric antigen receptor (CAR) T cells. The latter, in particular, has revolutionized the treatment of hematologic malignancies. However, the efficacy against solid tumor is still sparse. Major limitations include the following: severe toxicities, restricted infiltration and activation within the tumors, antigen escape and heterogeneity, and manufacturing issues. ACT is a promising tool to improve the outcome of metastatic NSCLC, but significant translational and clinical research is needed to improve its application and expand the use in NSCLC.

摘要

综述目的

在本文中,我们回顾了非小细胞肺癌(NSCLC)中过继性细胞疗法(ACT)的现状和方式。我们还讨论了阻碍ACT应用的挑战以及克服这些障碍的方法。

最新发现

多项试验正在进行,以研究基于T细胞的ACT的三种主要方式:肿瘤浸润淋巴细胞(TILs)、基因工程T细胞受体(TCRs)和嵌合抗原受体(CAR)T细胞。尤其是后者,已经彻底改变了血液系统恶性肿瘤的治疗方式。然而,其对实体瘤的疗效仍然有限。主要局限性包括:严重毒性、肿瘤内浸润和激活受限、抗原逃逸和异质性以及生产问题。ACT是改善转移性NSCLC预后的一种有前景的工具,但需要大量的转化和临床研究来改进其应用并扩大其在NSCLC中的使用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27e7/10556121/979487fc8ffc/11912_2023_1443_Fig1_HTML.jpg

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