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Facts and Hopes in Immunotherapy of Soft-Tissue Sarcomas.软组织肉瘤的免疫治疗:事实与展望。
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本文引用的文献

1
Tumor mutation burden and checkpoint immunotherapy markers in primary and metastatic synovial sarcoma.原发和转移性滑膜肉瘤中的肿瘤突变负担和检查点免疫治疗标志物。
Hum Pathol. 2020 Jun;100:15-23. doi: 10.1016/j.humpath.2020.04.007. Epub 2020 May 5.
2
Prevalence of PD-L1 expression in matched recurrent and/or metastatic sarcoma samples and in a range of selected sarcomas subtypes.在匹配的复发性和/或转移性肉瘤样本以及一系列选定的肉瘤亚型中,PD-L1 表达的流行率。
PLoS One. 2020 Apr 15;15(4):e0222551. doi: 10.1371/journal.pone.0222551. eCollection 2020.
3
A comparative view on the expression patterns of PD-L1 and PD-1 in soft tissue sarcomas.软组织肉瘤中 PD-L1 和 PD-1 表达模式的比较观察。
Cancer Immunol Immunother. 2020 Jul;69(7):1353-1362. doi: 10.1007/s00262-020-02552-5. Epub 2020 Mar 28.
4
The clinical outcomes of undifferentiated pleomorphic sarcoma (UPS): A single-centre experience of two decades with the assessment of PD-L1 expressions.未分化多形性肉瘤(UPS)的临床结果:单中心二十年经验及 PD-L1 表达评估。
Eur J Surg Oncol. 2020 Jul;46(7):1287-1293. doi: 10.1016/j.ejso.2020.02.029. Epub 2020 Feb 24.
5
Pazopanib for treatment of typical solitary fibrous tumours: a multicentre, single-arm, phase 2 trial.帕唑帕尼治疗典型孤立性纤维瘤:多中心、单臂、2 期临床试验。
Lancet Oncol. 2020 Mar;21(3):456-466. doi: 10.1016/S1470-2045(19)30826-5. Epub 2020 Feb 14.
6
The Angiosarcoma Project: enabling genomic and clinical discoveries in a rare cancer through patient-partnered research.血管肉瘤计划:通过患者合作研究,在罕见癌症中实现基因组和临床发现。
Nat Med. 2020 Feb;26(2):181-187. doi: 10.1038/s41591-019-0749-z. Epub 2020 Feb 10.
7
Objective Response Rate Among Patients With Locally Advanced or Metastatic Sarcoma Treated With Talimogene Laherparepvec in Combination With Pembrolizumab: A Phase 2 Clinical Trial.接受替莫唑胺联合替莫唑胺治疗的局部晚期或转移性肉瘤患者的客观缓解率:一项 2 期临床试验。
JAMA Oncol. 2020 Mar 1;6(3):402-408. doi: 10.1001/jamaoncol.2019.6152.
8
Genome-wide CRISPR-Cas9 screening reveals ubiquitous T cell cancer targeting via the monomorphic MHC class I-related protein MR1.全基因组 CRISPR-Cas9 筛选揭示了通过单态 MHC Ⅰ类相关蛋白 MR1 对普遍存在的 T 细胞癌症进行靶向治疗。
Nat Immunol. 2020 Feb;21(2):178-185. doi: 10.1038/s41590-019-0578-8. Epub 2020 Jan 20.
9
B cells are associated with survival and immunotherapy response in sarcoma.B 细胞与肉瘤的生存和免疫治疗反应有关。
Nature. 2020 Jan;577(7791):556-560. doi: 10.1038/s41586-019-1906-8. Epub 2020 Jan 15.
10
CD73 immune checkpoint defines regulatory NK cells within the tumor microenvironment.CD73 免疫检查点在肿瘤微环境中定义调节性 NK 细胞。
J Clin Invest. 2020 Mar 2;130(3):1185-1198. doi: 10.1172/JCI128895.

软组织肉瘤的免疫治疗:事实与展望。

Facts and Hopes in Immunotherapy of Soft-Tissue Sarcomas.

机构信息

University Hospital Virgen del Rocio, Seville, Spain.

Institute of Biomedicine of Seville (HUVR; CSIC; US), Seville, Spain.

出版信息

Clin Cancer Res. 2020 Nov 15;26(22):5801-5808. doi: 10.1158/1078-0432.CCR-19-3335. Epub 2020 Jun 29.

DOI:10.1158/1078-0432.CCR-19-3335
PMID:32601077
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7669707/
Abstract

Sarcomas are mesenchymal tumors, encompassing more than 175 subtypes, each one with their own genetic complexities. As a result, immunotherapy approaches have not been universally successful across the wide range of diverse subtypes. The actual state of science and the current clinical data utilizing immunotherapy within the soft-tissue sarcomas (STS) will be detailed in this review. More precisely, the review will focus on: (i) the role of the immune microenvironment in the development and activity of new therapeutic approaches; (ii) the recent identification of the sarcoma immune class (SIC) groups, especially group SIC E with its B-cell signature that predicts immunotherapy response; (iii) the clinical trials using PD-1 and/or CTLA-4 inhibitors, which serves as reference for response data, (iv) the promising clinical activity from the combination of anti-angiogenics agents with PD-1 inhibitors, (v) the adapted T-cell therapies for synovial sarcoma that target either NY-ESO or MAGEA4; and (vi) the role for localized therapy using the virotherapy T-VEC with PD-1 inhibitors. Herein, we present the facts and the hopes for the patients with sarcoma, as the field is rapidly advancing its understanding of what and where to use the various types of immunotherapies.

摘要

肉瘤是间叶组织肿瘤,包含超过 175 种亚型,每种亚型都有其自身的遗传复杂性。因此,免疫疗法在广泛的不同亚型中并非普遍有效。本文将详细介绍软组织肉瘤(STS)中免疫疗法的科学现状和当前临床数据。更具体地说,该综述将重点关注:(i)免疫微环境在新治疗方法的发展和活性中的作用;(ii)最近确定的肉瘤免疫分类(SIC)组,特别是具有预测免疫治疗反应的 B 细胞特征的 SIC E 组;(iii)使用 PD-1 和/或 CTLA-4 抑制剂的临床试验,作为反应数据的参考;(iv)抗血管生成药物与 PD-1 抑制剂联合应用的有前途的临床活性;(v)针对 NY-ESO 或 MAGEA4 的滑膜肉瘤的适应性 T 细胞疗法;以及(vi)使用 PD-1 抑制剂的病毒疗法 T-VEC 进行局部治疗的作用。在这里,我们为肉瘤患者呈现了事实和希望,因为该领域正在迅速加深对使用各种类型免疫疗法的认识。