Immune Checkpoint Blockade and Emerging Combination Platforms in Breast Cancer: A Narrative Review.

IF 3.6 4区 医学 Q2 ONCOLOGY
Breast Cancer : Targets and Therapy Pub Date : 2026-05-05 eCollection Date: 2026-01-01 DOI:10.2147/BCTT.S588323
Maryam Abbaspour, Nafiseh Esmaeil, Vajihe Akbari, Mohammad Ghoreishi, Haniyeh Rafiepoor
{"title":"Immune Checkpoint Blockade and Emerging Combination Platforms in Breast Cancer: A Narrative Review.","authors":"Maryam Abbaspour, Nafiseh Esmaeil, Vajihe Akbari, Mohammad Ghoreishi, Haniyeh Rafiepoor","doi":"10.2147/BCTT.S588323","DOIUrl":null,"url":null,"abstract":"<p><p>This narrative review examines recent progress in immunotherapy for breast cancer (BC), focusing on immune checkpoint inhibitors (ICIs) alone and in combination with other modalities. Landmark trials such as KEYNOTE-522 and IMpassion130 have established the efficacy of pembrolizumab and atezolizumab in triple-negative breast cancer (TNBC). However, BC remains a leading cause of cancer-related fatalities, underscoring the need for novel approaches. We synthesize combination strategies into three mechanistic categories: (I) those that remodel the immunosuppressive tumor microenvironment (chemotherapy, PARP inhibitors, oncolytic viruses); (II) those that enhance effector cell persistence (CAR-T, CAR-NK, cytokine support); and (III) those that modulate immune checkpoint axes beyond PD-1/CTLA-4 (LAG-3, TIM-3, TIGIT). Combining ICIs with CAR-T cells, CAR-NK cells, oncolytic viruses, and exosomes has been shown to improve antitumor immune responses. This review provides a translational framework for biomarker-driven patient stratification and critically evaluates the clinical maturity of emerging platforms. Further research and clinical trials are needed to expand applicability across BC subtypes and improve patient outcomes.</p>","PeriodicalId":9106,"journal":{"name":"Breast Cancer : Targets and Therapy","volume":"18 ","pages":"588323"},"PeriodicalIF":3.6000,"publicationDate":"2026-05-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13157352/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Breast Cancer : Targets and Therapy","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.2147/BCTT.S588323","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

This narrative review examines recent progress in immunotherapy for breast cancer (BC), focusing on immune checkpoint inhibitors (ICIs) alone and in combination with other modalities. Landmark trials such as KEYNOTE-522 and IMpassion130 have established the efficacy of pembrolizumab and atezolizumab in triple-negative breast cancer (TNBC). However, BC remains a leading cause of cancer-related fatalities, underscoring the need for novel approaches. We synthesize combination strategies into three mechanistic categories: (I) those that remodel the immunosuppressive tumor microenvironment (chemotherapy, PARP inhibitors, oncolytic viruses); (II) those that enhance effector cell persistence (CAR-T, CAR-NK, cytokine support); and (III) those that modulate immune checkpoint axes beyond PD-1/CTLA-4 (LAG-3, TIM-3, TIGIT). Combining ICIs with CAR-T cells, CAR-NK cells, oncolytic viruses, and exosomes has been shown to improve antitumor immune responses. This review provides a translational framework for biomarker-driven patient stratification and critically evaluates the clinical maturity of emerging platforms. Further research and clinical trials are needed to expand applicability across BC subtypes and improve patient outcomes.

乳腺癌免疫检查点阻断和新出现的联合治疗平台:综述
本文综述了乳腺癌(BC)免疫治疗的最新进展,重点是免疫检查点抑制剂(ICIs)单独使用和与其他方式联合使用。KEYNOTE-522和IMpassion130等具有里程碑意义的试验已经确定了派姆单抗和atezolizumab治疗三阴性乳腺癌(TNBC)的疗效。然而,BC仍然是癌症相关死亡的主要原因,强调了对新方法的需求。我们将联合策略分为三种机制类别:(I)那些重塑免疫抑制肿瘤微环境的策略(化疗、PARP抑制剂、溶瘤病毒);(II)增强效应细胞持久性(CAR-T, CAR-NK,细胞因子支持);(III)调节PD-1/CTLA-4以外的免疫检查点轴(LAG-3, TIM-3, TIGIT)。ICIs与CAR-T细胞、CAR-NK细胞、溶瘤病毒和外泌体联合使用已被证明可改善抗肿瘤免疫反应。这篇综述为生物标志物驱动的患者分层提供了一个翻译框架,并批判性地评估了新兴平台的临床成熟度。需要进一步的研究和临床试验来扩大BC亚型的适用性并改善患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
4.10
自引率
0.00%
发文量
40
审稿时长
16 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书