• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

见树又见林:TIL 与 PD-L1 作为免疫生物标志物。

Seeing the forest and the tree: TILs and PD-L1 as immune biomarkers.

机构信息

Peter MacCallum Cancer Centre, Melbourne, VIC, 3000, Australia.

Sir Peter MacCallum Department of Oncology, The University of Melbourne, Victoria, 3010, Australia.

出版信息

Breast Cancer Res Treat. 2021 Oct;189(3):599-606. doi: 10.1007/s10549-021-06287-4. Epub 2021 Sep 6.

DOI:10.1007/s10549-021-06287-4
PMID:34487294
Abstract

Here we will provide an immune-focussed overview of biomarkers in early and advanced stage breast cancer. It should be noted from the outset that all the biomarkers under discussion here have not been tested in prospective clinical trials to determine their predictive performance. Such trials require very large sample sizes due to the statistical burden of testing an interaction between a treatment and a biomarker, which is compounded by the heterogeneous biology of breast cancer (Polley et al. in J Natl Cancer Inst 105:1677-1683 2013 [1]). For a detailed discussion of the immunobiology of breast cancer, analytical aspects of these biomarkers, emerging biomarkers such as tumour mutation burden and detailed immunotherapy clinical trial data, see other articles in this issue.

摘要

在这里,我们将提供一个针对早期和晚期乳腺癌生物标志物的免疫重点概述。应该从一开始就注意到,这里讨论的所有生物标志物都没有经过前瞻性临床试验来确定它们的预测性能。由于需要测试治疗与生物标志物之间相互作用的统计学负担,以及乳腺癌生物学的异质性(Polley 等人,J Natl Cancer Inst 105:1677-1683,2013 [1]),因此此类试验需要非常大的样本量。有关乳腺癌免疫生物学、这些生物标志物的分析方面、肿瘤突变负担和详细免疫治疗临床试验数据等新兴生物标志物的详细讨论,请参阅本期的其他文章。

相似文献

1
Seeing the forest and the tree: TILs and PD-L1 as immune biomarkers.见树又见林:TIL 与 PD-L1 作为免疫生物标志物。
Breast Cancer Res Treat. 2021 Oct;189(3):599-606. doi: 10.1007/s10549-021-06287-4. Epub 2021 Sep 6.
2
Integration of tumour infiltrating lymphocytes, programmed cell-death ligand-1, CD8 and FOXP3 in prognostic models for triple-negative breast cancer: Analysis of 244 stage I-III patients treated with standard therapy.肿瘤浸润淋巴细胞、程序性细胞死亡配体-1、CD8 和 FOXP3 在三阴性乳腺癌预后模型中的整合:对 244 例接受标准治疗的 I-III 期患者的分析。
Eur J Cancer. 2020 Sep;136:7-15. doi: 10.1016/j.ejca.2020.05.014. Epub 2020 Jul 1.
3
Programmed death-ligand 1 (PD-L1) expression in tumour cell and tumour infiltrating lymphocytes of HER2-positive breast cancer and its prognostic value.HER2 阳性乳腺癌中肿瘤细胞和肿瘤浸润淋巴细胞程序性死亡配体 1(PD-L1)的表达及其预后价值。
Sci Rep. 2017 Sep 15;7(1):11671. doi: 10.1038/s41598-017-11905-7.
4
FDG uptake reflects breast cancer immunological features: the PD-L1 expression and degree of TILs in primary breast cancer.氟代脱氧葡萄糖摄取反映乳腺癌免疫特征:原发性乳腺癌中 PD-L1 表达和肿瘤浸润淋巴细胞的程度。
Breast Cancer Res Treat. 2020 Jun;181(2):331-338. doi: 10.1007/s10549-020-05619-0. Epub 2020 Apr 6.
5
PD-L1 expression in tumor infiltrated lymphocytes predicts survival in triple-negative breast cancer.肿瘤浸润淋巴细胞中的 PD-L1 表达可预测三阴性乳腺癌的生存情况。
Pathol Res Pract. 2020 Mar;216(3):152802. doi: 10.1016/j.prp.2019.152802. Epub 2019 Dec 24.
6
A radiomics approach to assess tumour-infiltrating CD8 cells and response to anti-PD-1 or anti-PD-L1 immunotherapy: an imaging biomarker, retrospective multicohort study.一种基于放射组学的方法来评估肿瘤浸润 CD8 细胞与抗 PD-1 或抗 PD-L1 免疫治疗反应的关系:一项影像学生物标志物、回顾性多队列研究。
Lancet Oncol. 2018 Sep;19(9):1180-1191. doi: 10.1016/S1470-2045(18)30413-3. Epub 2018 Aug 14.
7
Expression of PD-L1 Attenuates the Positive Impacts of High-level Tumor-infiltrating Lymphocytes on Prognosis of Triple-negative Breast Cancer.PD-L1 的表达减弱了高水平肿瘤浸润淋巴细胞对三阴性乳腺癌预后的积极影响。
Cancer Biol Ther. 2019;20(8):1105-1112. doi: 10.1080/15384047.2019.1595282. Epub 2019 Mar 31.
8
An Immunoscore Using PD-L1, CD68, and Tumor-infiltrating Lymphocytes (TILs) to Predict Response to Neoadjuvant Chemotherapy in Invasive Breast Cancer.一种使用程序性死亡受体配体1(PD-L1)、CD68和肿瘤浸润淋巴细胞(TILs)预测浸润性乳腺癌新辅助化疗反应的免疫评分
Appl Immunohistochem Mol Morphol. 2018 Oct;26(9):611-619. doi: 10.1097/PAI.0000000000000485.
9
The therapeutic candidate for immune checkpoint inhibitors elucidated by the status of tumor-infiltrating lymphocytes (TILs) and programmed death ligand 1 (PD-L1) expression in triple negative breast cancer (TNBC).免疫检查点抑制剂的治疗候选物由三阴性乳腺癌(TNBC)中肿瘤浸润淋巴细胞(TILs)和程序性死亡配体 1(PD-L1)表达的状态所阐明。
Breast Cancer. 2018 Jan;25(1):34-42. doi: 10.1007/s12282-017-0781-0. Epub 2017 May 9.
10
Relevance of tumour-infiltrating lymphocytes, PD-1 and PD-L1 in patients with high-risk, nodal-metastasised breast cancer of the German Adjuvant Intergroup Node-positive study.德国辅助性肿瘤组淋巴结阳性研究中高危、淋巴结转移的乳腺癌患者肿瘤浸润淋巴细胞、PD-1 和 PD-L1 的相关性。
Eur J Cancer. 2019 Jun;114:76-88. doi: 10.1016/j.ejca.2019.04.010. Epub 2019 May 7.

引用本文的文献

1
The prognostic value of a combined immune score in tumor and immune cells assessed by immunohistochemistry in triple-negative breast cancer.免疫组织化学评估的肿瘤和免疫细胞联合免疫评分在三阴性乳腺癌中的预后价值。
Breast Cancer Res. 2023 Nov 3;25(1):134. doi: 10.1186/s13058-023-01710-8.
2
Tumor-infiltrating lymphocytes provides recent survival information for early-stage HER2-low-positive breast cancer: a large cohort retrospective study.肿瘤浸润淋巴细胞为早期HER2低表达阳性乳腺癌提供近期生存信息:一项大型队列回顾性研究
Front Oncol. 2023 Jun 20;13:1148228. doi: 10.3389/fonc.2023.1148228. eCollection 2023.
3
Core needle biopsies alter the amounts of CCR5, Siglec-15, and PD-L1 positivities in breast carcinoma.

本文引用的文献

1
PD-L1 Immunohistochemistry Assay Comparison in Atezolizumab Plus nab-Paclitaxel-Treated Advanced Triple-Negative Breast Cancer.阿替利珠单抗联合白蛋白紫杉醇治疗晚期三阴性乳腺癌中 PD-L1 免疫组织化学检测方法的比较。
J Natl Cancer Inst. 2021 Nov 29;113(12):1733-1743. doi: 10.1093/jnci/djab108.
2
Tumour-infiltrating lymphocytes as a prognostic and tamoxifen predictive marker in premenopausal breast cancer: data from a randomised trial with long-term follow-up.肿瘤浸润淋巴细胞作为绝经前乳腺癌的预后和他莫昔芬预测标志物:来自一项具有长期随访的随机试验的数据。
Breast Cancer Res. 2020 Dec 23;22(1):140. doi: 10.1186/s13058-020-01364-w.
3
核心针活检改变乳腺癌中 CCR5、Siglec-15 和 PD-L1 阳性的数量。
Virchows Arch. 2023 Aug;483(2):215-224. doi: 10.1007/s00428-023-03563-0. Epub 2023 May 24.
4
Triple-Negative Breast Cancer and Predictive Markers of Response to Neoadjuvant Chemotherapy: A Systematic Review.三阴性乳腺癌与新辅助化疗反应的预测标志物:一项系统综述。
Int J Mol Sci. 2023 Feb 3;24(3):2969. doi: 10.3390/ijms24032969.
5
The Great Immune Escape: Understanding the Divergent Immune Response in Breast Cancer Subtypes.免疫大逃脱:理解乳腺癌亚型中的不同免疫反应。
Cancer Discov. 2023 Jan 9;13(1):23-40. doi: 10.1158/2159-8290.CD-22-0475.
6
Integrative prognostic analysis of tumor-infiltrating lymphocytes, CD8, CD20, programmed cell death-ligand 1, and tertiary lymphoid structures in patients with early-stage triple-negative breast cancer who did not receive adjuvant chemotherapy.未接受辅助化疗的早期三阴性乳腺癌患者肿瘤浸润淋巴细胞、CD8、CD20、程序性细胞死亡配体 1 和三级淋巴结构的综合预后分析。
Breast Cancer Res Treat. 2023 Jan;197(2):287-297. doi: 10.1007/s10549-022-06787-x. Epub 2022 Nov 16.
7
Clinicopathological characteristics and prognostic analysis of tumor-infiltrating lymphocytes (TILs) in ductal carcinoma in situ (DCIS) and DCIS with microinvasion (DCIS-Mi) of the breast.乳腺导管原位癌(DCIS)及微浸润性导管原位癌(DCIS-Mi)中肿瘤浸润淋巴细胞(TILs)的临床病理特征及预后分析。
Breast Cancer Res Treat. 2022 May;193(1):111-120. doi: 10.1007/s10549-022-06553-z. Epub 2022 Mar 8.
8
Tumor Cell-Autonomous Pro-Metastatic Activities of PD-L1 in Human Breast Cancer Are Mediated by PD-L1-S283 and Chemokine Axes.人乳腺癌中PD-L1的肿瘤细胞自主促转移活性由PD-L1-S283和趋化因子轴介导。
Cancers (Basel). 2022 Feb 18;14(4):1042. doi: 10.3390/cancers14041042.
9
Incorporation of TILs in daily breast cancer care: how much evidence can we bear?将 TIL 纳入乳腺癌常规护理:我们能承受多少证据?
Virchows Arch. 2022 Jan;480(1):147-162. doi: 10.1007/s00428-022-03276-w. Epub 2022 Jan 19.
BRD9 Is a Critical Regulator of Androgen Receptor Signaling and Prostate Cancer Progression.
BRD9是雄激素受体信号传导和前列腺癌进展的关键调节因子。
Cancer Res. 2021 Feb 15;81(4):820-833. doi: 10.1158/0008-5472.CAN-20-1417. Epub 2020 Dec 21.
4
Pembrolizumab plus chemotherapy versus placebo plus chemotherapy for previously untreated locally recurrent inoperable or metastatic triple-negative breast cancer (KEYNOTE-355): a randomised, placebo-controlled, double-blind, phase 3 clinical trial.帕博利珠单抗联合化疗对比安慰剂联合化疗用于治疗既往未经治疗的局部晚期不可切除或转移性三阴性乳腺癌(KEYNOTE-355):一项随机、安慰剂对照、双盲、III 期临床研究。
Lancet. 2020 Dec 5;396(10265):1817-1828. doi: 10.1016/S0140-6736(20)32531-9.
5
Diagnostic approach to the evaluation of myeloid malignancies following CAR T-cell therapy in B-cell acute lymphoblastic leukemia.CAR T 细胞治疗后 B 细胞急性淋巴细胞白血病继发髓系恶性肿瘤的评估:诊断方法。
J Immunother Cancer. 2020 Nov;8(2). doi: 10.1136/jitc-2020-001563.
6
How current assay approval policies are leading to unintended imprecision medicine.当前的检测批准政策是如何导致非预期的精准医学不精确性的。
Lancet Oncol. 2020 Nov;21(11):1399-1401. doi: 10.1016/S1470-2045(20)30592-1. Epub 2020 Oct 21.
7
Trastuzumab emtansine plus atezolizumab versus trastuzumab emtansine plus placebo in previously treated, HER2-positive advanced breast cancer (KATE2): a phase 2, multicentre, randomised, double-blind trial.恩美曲妥珠单抗联合阿替利珠单抗对比恩美曲妥珠单抗联合安慰剂用于既往治疗、HER2 阳性晚期乳腺癌(KATE2):一项 2 期、多中心、随机、双盲试验。
Lancet Oncol. 2020 Oct;21(10):1283-1295. doi: 10.1016/S1470-2045(20)30465-4.
8
Neoadjuvant atezolizumab in combination with sequential nab-paclitaxel and anthracycline-based chemotherapy versus placebo and chemotherapy in patients with early-stage triple-negative breast cancer (IMpassion031): a randomised, double-blind, phase 3 trial.早期三阴性乳腺癌患者新辅助阿替利珠单抗联合序贯纳武利尤单抗和基于蒽环类的化疗与安慰剂和化疗相比:一项随机、双盲、III 期试验(IMpassion031)。
Lancet. 2020 Oct 10;396(10257):1090-1100. doi: 10.1016/S0140-6736(20)31953-X. Epub 2020 Sep 20.
9
Effect of Eribulin With or Without Pembrolizumab on Progression-Free Survival for Patients With Hormone Receptor-Positive, ERBB2-Negative Metastatic Breast Cancer: A Randomized Clinical Trial.厄瑞布林联合或不联合帕博利珠单抗治疗激素受体阳性、HER2 阴性转移性乳腺癌患者的无进展生存期:一项随机临床试验。
JAMA Oncol. 2020 Oct 1;6(10):1598-1605. doi: 10.1001/jamaoncol.2020.3524.
10
Tumor-infiltrating lymphocytes (TILs) in ER+/HER2- breast cancer.ER+/HER2- 乳腺癌中的肿瘤浸润淋巴细胞(TILs)。
Breast Cancer Res Treat. 2020 Sep;183(2):347-354. doi: 10.1007/s10549-020-05771-7. Epub 2020 Jul 3.