» Articles » PMID: 39062758

Immunotherapy in Breast Cancer

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2024 Jul 27
PMID 39062758
Authors
Affiliations
Soon will be listed here.
Abstract

Breast cancer is a disease encompassing a spectrum of molecular subtypes and clinical presentations, each with distinct prognostic implications and treatment responses. Breast cancer has traditionally been considered an immunologically "cold" tumor, unresponsive to immunotherapy. However, clinical trials in recent years have found immunotherapy to be an efficacious therapeutic option for select patients. Breast cancer is categorized into different subtypes ranging from the most common positive hormone receptor (HR+), human epidermal growth factor receptor 2 (HER2)-negative type, to less frequent HER2- positive breast cancer and triple-negative breast cancer (TNBC), highlighting the necessity for tailored treatment strategies aimed at maximizing patient outcomes. Despite notable progress in early detection and new therapeutic modalities, breast cancer remains the second leading cause of cancer death in the USA. Moreover, in recent decades, breast cancer incidence rates have been increasing, especially in women younger than the age of 50. This has prompted the exploration of new therapeutic approaches to address this trend, offering new therapeutic prospects for breast cancer patients. Immunotherapy is a class of therapeutic agents that has revolutionized the treatment landscape of many cancers, namely melanoma, lung cancer, and gastroesophageal cancers, amongst others. Though belatedly, immunotherapy has entered the treatment armamentarium of breast cancer, with the approval of pembrolizumab in combination with chemotherapy in triple-negative breast cancer (TNBC) in the neoadjuvant and advanced settings, thereby paving the path for further research and integration of immune checkpoint inhibitors in other subtypes of breast cancer. Trials exploring various combination therapies to harness the power of immunotherapy in symbiosis with various chemotherapeutic agents are ongoing in hopes of improving response rates and prolonging survival for breast cancer patients. Biomarkers and precise patient selection for the utilization of immunotherapy remain cardinal and are currently under investigation, with some biomarkers showing promise, such as Program Death Lignat-1 (PDL-1) Combined Positive Score, Tumor Mutation Burden (TMB), and Tumor Infiltrating Lymphocytes (TILs). This review will present the current landscape of immunotherapy, particularly checkpoint inhibitors, in different types of breast cancer.

Citing Articles

Unravelling the role of ubiquitin-specific proteases in breast carcinoma: insights into tumour progression and immune microenvironment modulation.

Yang H, Sun T, Sun Z, Wang H, Liu D, Wu D World J Surg Oncol. 2025; 23(1):60.

PMID: 39979972 PMC: 11841324. DOI: 10.1186/s12957-025-03667-8.


DNA methyltransferase 3A: A prognostic biomarker and potential target for immunotherapy in gastric cancer.

Wei Z, Kou Z, Luo Y, Cheng Y Medicine (Baltimore). 2025; 104(7):e41578.

PMID: 39960919 PMC: 11835108. DOI: 10.1097/MD.0000000000041578.


Dual Functions of Androgen Receptor Overexpression in Triple-Negative Breast Cancer: A Complex Prognostic Marker.

Kiraz U, Rewcastle E, Fykse S, Lundal I, Gudlaugsson E, Skaland I Bioengineering (Basel). 2025; 12(1).

PMID: 39851328 PMC: 11761274. DOI: 10.3390/bioengineering12010054.


Comparative analysis of the genomic and expression profiles of ANLN and KDR as prognostic markers in breast Cancer.

Mehmood A, Li R, Kaushik A, Wei D In Silico Pharmacol. 2025; 13(1):15.

PMID: 39831055 PMC: 11735758. DOI: 10.1007/s40203-024-00301-5.


Regulatory T cell-associated gene signature correlates with prognostic risk and immune infiltration in patients with breast cancer.

Wu J, Zhao G, Cai Y Transl Cancer Res. 2025; 13(12):6766-6781.

PMID: 39816556 PMC: 11729763. DOI: 10.21037/tcr-24-1118.


References
1.
Schmid P, Adams S, Rugo H, Schneeweiss A, Barrios C, Iwata H . Atezolizumab and Nab-Paclitaxel in Advanced Triple-Negative Breast Cancer. N Engl J Med. 2018; 379(22):2108-2121. DOI: 10.1056/NEJMoa1809615. View

2.
Cortes J, Cescon D, Rugo H, Nowecki Z, Im S, Yusof M . 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. Lancet. 2020; 396(10265):1817-1828. DOI: 10.1016/S0140-6736(20)32531-9. View

3.
Arnedos M, Bihan C, Delaloge S, Andre F . Triple-negative breast cancer: are we making headway at least?. Ther Adv Med Oncol. 2012; 4(4):195-210. PMC: 3384094. DOI: 10.1177/1758834012444711. View

4.
Ahn H, Sim S, Suh K, Kim M, Jeong J, Kim J . Response Rate and Safety of a Neoadjuvant Pertuzumab, Atezolizumab, Docetaxel, and Trastuzumab Regimen for Patients With ERBB2-Positive Stage II/III Breast Cancer: The Neo-PATH Phase 2 Nonrandomized Clinical Trial. JAMA Oncol. 2022; 8(9):1271-1277. PMC: 10881214. DOI: 10.1001/jamaoncol.2022.2310. View

5.
Corti C, Venetis K, Sajjadi E, Zattoni L, Curigliano G, Fusco N . CAR-T cell therapy for triple-negative breast cancer and other solid tumors: preclinical and clinical progress. Expert Opin Investig Drugs. 2022; 31(6):593-605. DOI: 10.1080/13543784.2022.2054326. View