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Update on current and new potential immunotherapies in breast cancer, from bench to bedside.

作者信息

Alaluf Emmanuelle, Shalamov Michal Mia, Sonnenblick Amir

机构信息

Medical Oncology Clinic, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.

Department of Immunology, Weizmann Institute of Science, Rehovot, Israel.

出版信息

Front Immunol. 2024 Feb 15;15:1287824. doi: 10.3389/fimmu.2024.1287824. eCollection 2024.


DOI:10.3389/fimmu.2024.1287824
PMID:38433837
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10905744/
Abstract

Impressive advances have been seen in cancer immunotherapy during the last years. Although breast cancer (BC) has been long considered as non-immunogenic, immunotherapy for the treatment of BC is now emerging as a new promising therapeutic approach with considerable potential. This is supported by a plethora of completed and ongoing preclinical and clinical studies in various types of immunotherapies. However, a significant gap between clinical oncology and basic cancer research impairs the understanding of cancer immunology and immunotherapy, hampering cancer therapy research and development. To exploit the accumulating available data in an optimal way, both fundamental mechanisms at play in BC immunotherapy and its clinical pitfalls must be integrated. Then, clinical trials must be critically designed with appropriate combinations of conventional and immunotherapeutic strategies. While there is room for major improvement, this updated review details the immunotherapeutic tools available to date, from bench to bedside, in the hope that this will lead to rethinking and optimizing standards of care for BC patients.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cc1/10905744/ffc6785be7d0/fimmu-15-1287824-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cc1/10905744/040101b88d6b/fimmu-15-1287824-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cc1/10905744/7d41c4077626/fimmu-15-1287824-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cc1/10905744/fe36c5337db9/fimmu-15-1287824-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cc1/10905744/83381e0dac6c/fimmu-15-1287824-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cc1/10905744/3e7cef39bbb3/fimmu-15-1287824-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cc1/10905744/d4a4ba01a334/fimmu-15-1287824-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cc1/10905744/5eb7cb111d71/fimmu-15-1287824-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cc1/10905744/6b4dd37335fb/fimmu-15-1287824-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cc1/10905744/ffc6785be7d0/fimmu-15-1287824-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cc1/10905744/040101b88d6b/fimmu-15-1287824-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cc1/10905744/7d41c4077626/fimmu-15-1287824-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cc1/10905744/fe36c5337db9/fimmu-15-1287824-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cc1/10905744/83381e0dac6c/fimmu-15-1287824-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cc1/10905744/3e7cef39bbb3/fimmu-15-1287824-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cc1/10905744/d4a4ba01a334/fimmu-15-1287824-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cc1/10905744/5eb7cb111d71/fimmu-15-1287824-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cc1/10905744/6b4dd37335fb/fimmu-15-1287824-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cc1/10905744/ffc6785be7d0/fimmu-15-1287824-g009.jpg

相似文献

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引用本文的文献

[1]
The interplay between the immune response and neoadjuvant therapy in breast cancer.

Front Oncol. 2025-5-12

[2]
Bispecific antibodies and CLEM: an analytical approach to advanced cell imaging for therapeutic strategies.

Appl Microsc. 2025-1-20

[3]
Polyphenols as Immunomodulators and Epigenetic Modulators: An Analysis of Their Role in the Treatment and Prevention of Breast Cancer.

Nutrients. 2024-11-29

[4]
Revolutionizing adjuvant development: harnessing AI for next-generation cancer vaccines.

Front Immunol. 2024

本文引用的文献

[1]
Phase I Trial of Autologous RNA-electroporated cMET-directed CAR T Cells Administered Intravenously in Patients with Melanoma and Breast Carcinoma.

Cancer Res Commun. 2023-5

[2]
CCL19 dendritic cells potentiate clinical benefit of anti-PD-(L)1 immunotherapy in triple-negative breast cancer.

Med. 2023-6-9

[3]
Obesity Is Associated with Immunometabolic Changes in Adipose Tissue That May Drive Treatment Resistance in Breast Cancer: Immune-Metabolic Reprogramming and Novel Therapeutic Strategies.

Cancers (Basel). 2023-4-24

[4]
Deciphering the Immunomodulatory Role of Cyclin-Dependent Kinase 4/6 Inhibitors in the Tumor Microenvironment.

Int J Mol Sci. 2023-1-23

[5]
PET/CT with Fibroblast Activation Protein Inhibitors in Breast Cancer: Diagnostic and Theranostic Application-A Literature Review.

Cancers (Basel). 2023-1-31

[6]
Macrophage and monocyte subsets as new therapeutic targets in cancer immunotherapy.

ESMO Open. 2023-2

[7]
Anti-TGF-β/PD-L1 bispecific antibody promotes T cell infiltration and exhibits enhanced antitumor activity in triple-negative breast cancer.

J Immunother Cancer. 2022-12

[8]
Margetuximab Versus Trastuzumab in Patients With Previously Treated HER2-Positive Advanced Breast Cancer (SOPHIA): Final Overall Survival Results From a Randomized Phase 3 Trial.

J Clin Oncol. 2023-1-10

[9]
Safety and Outcomes of a Plasmid DNA Vaccine Encoding the ERBB2 Intracellular Domain in Patients With Advanced-Stage ERBB2-Positive Breast Cancer: A Phase 1 Nonrandomized Clinical Trial.

JAMA Oncol. 2023-1-1

[10]
Lactate score predicts survival, immune cell infiltration and response to immunotherapy in breast cancer.

Front Genet. 2022-8-15

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