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Advancements and challenges in triple-negative breast cancer: a comprehensive review of therapeutic and diagnostic strategies.

作者信息

Xiong Nating, Wu Heming, Yu Zhikang

机构信息

Department of Blood Transfusion, Meizhou People's Hospital, Meizhou Academy of Medical Sciences, Meizhou, China.

Meizhou Municipal Engineering and Technology Research Centre for Molecular Diagnostics of Major Genetic Disorders, Meizhou People's Hospital, Meizhou, China.

出版信息

Front Oncol. 2024 May 28;14:1405491. doi: 10.3389/fonc.2024.1405491. eCollection 2024.


DOI:10.3389/fonc.2024.1405491
PMID:38863622
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11165151/
Abstract

Triple-negative breast cancer (TNBC) poses significant challenges in oncology due to its aggressive nature, limited treatment options, and poorer prognosis compared to other breast cancer subtypes. This comprehensive review examines the therapeutic and diagnostic landscape of TNBC, highlighting current strategies, emerging therapies, and future directions. Targeted therapies, including PARP inhibitors, immune checkpoint inhibitors, and EGFR inhibitors, hold promise for personalized treatment approaches. Challenges in identifying novel targets, exploring combination therapies, and developing predictive biomarkers must be addressed to optimize targeted therapy in TNBC. Immunotherapy represents a transformative approach in TNBC treatment, yet challenges in biomarker identification, combination strategies, and overcoming resistance persist. Precision medicine approaches offer opportunities for tailored treatment based on tumor biology, but integration of multi-omics data and clinical implementation present challenges requiring innovative solutions. Despite these challenges, ongoing research efforts and collaborative initiatives offer hope for improving outcomes and advancing treatment strategies in TNBC. By addressing the complexities of TNBC biology and developing effective therapeutic approaches, personalized treatments can be realized, ultimately enhancing the lives of TNBC patients. Continued research, clinical trials, and interdisciplinary collaborations are essential for realizing this vision and making meaningful progress in TNBC management.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7bf8/11165151/b3b9498fe1ca/fonc-14-1405491-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7bf8/11165151/2f9fcc50d496/fonc-14-1405491-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7bf8/11165151/b3b9498fe1ca/fonc-14-1405491-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7bf8/11165151/2f9fcc50d496/fonc-14-1405491-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7bf8/11165151/b3b9498fe1ca/fonc-14-1405491-g002.jpg

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本文引用的文献

[1]
Optical nanomaterial-based detection of biomarkers in liquid biopsy.

J Hematol Oncol. 2024-3-14

[2]
Targeting Receptor Tyrosine Kinases as a Novel Strategy for the Treatment of Triple-Negative Breast Cancer.

Technol Cancer Res Treat. 2024

[3]
Optimising first-line subtyping-based therapy in triple-negative breast cancer (FUTURE-SUPER): a multi-cohort, randomised, phase 2 trial.

Lancet Oncol. 2024-2

[4]
Liquid Biopsy: An Evolving Paradigm for Non-invasive Disease Diagnosis and Monitoring in Medicine.

Cureus. 2023-12-8

[5]
More Than Meets the Eye: A Case of Breast Cancer Switching from Being Luminal-Androgen-Receptor-Positive to Being Hormone-Receptor-Positive.

Medicina (Kaunas). 2023-10-22

[6]
Progressing nanotechnology to improve targeted cancer treatment: overcoming hurdles in its clinical implementation.

Mol Cancer. 2023-10-9

[7]
The Prediction Analysis of Microarray 50 (PAM50) Gene Expression Classifier Utilized in Indeterminate-Risk Breast Cancer Patients in Hungary: A Consecutive 5-Year Experience.

Genes (Basel). 2023-8-28

[8]
Recent advances in targeted strategies for triple-negative breast cancer.

J Hematol Oncol. 2023-8-28

[9]
Challenges and Opportunities in Developing Targeted Therapies for Triple Negative Breast Cancer.

Biomolecules. 2023-8-1

[10]
Advancing Breast Cancer Heterogeneity Analysis: Insights from Genomics, Transcriptomics and Proteomics at Bulk and Single-Cell Levels.

Cancers (Basel). 2023-8-18

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