乳腺癌:一种异质性病理。预测和预测因素-叙述性回顾。

IF 0.8 Q4 SURGERY
Chirurgia Pub Date : 2025-02-01 DOI:10.21614/chirurgia.3100
Maria-Teodora Popa, Aniela Nodiţi, Teodora-Mihaela Peleaşă, Smaranda Stoleru, Alexandru Blidaru
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引用次数: 0

摘要

乳腺癌(BC)是全球公认的影响女性的主要恶性肿瘤之一。其显著的异质性是一个决定性的特征,有助于疾病进展的不同模式和不同的治疗反应。这篇综述探讨了乳腺癌分类的演变,重点是关键的预后和预测因素。它检查传统的系统,如TNM分期和组织学分化,同时也结合现代元素,如分子亚型、基因组改变和先进的诊断分析。通过将经典的临床病理学见解与尖端的分子遗传技术相结合,我们的目标是提高治疗策略的准确性,最终提高我们对这种复杂疾病的理解和管理。该审查还强调了全球视角的重要性,因为实现主要治疗目标——延长生存期和提高生活质量——需要在更广泛、更全面的背景下处理该疾病。乳腺癌的复杂性,由肿瘤间和肿瘤内的显著变异性驱动,对传统的诊断和治疗方法提出了重大挑战。然而,基因组研究的突破,如分子图谱和基因检测,加深了我们对这种癌症复杂本质的理解。这些进展导致了关键基因改变的鉴定,包括BRCA1/2、TP53、PALB2、PTEN和PIK3CA的突变,这些突变深刻地影响肿瘤行为、治疗效果和患者预后。像Oncotype DX、MammaPrint、PROSIGNA和endopdict这样的基因组分析为复发风险和治疗选择提供了有价值的见解,强调了精准医疗日益增长的重要性。此外,分子肿瘤委员会的实施进一步加强了个性化的治疗策略,有助于改善患者的预后和生存率。这篇综述强调了量身定制治疗方法的重要性,并强调了乳腺癌在临床实践中的动态演变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Breast Cancer: A Heterogeneous Pathology. Prognostic and Predictive Factors - A Narrative Review.

Breast cancer (BC) is recognized as one of the leading malignancies affecting women worldwide. Its remarkable heterogeneity is a defining characteristic, contributing to both diverse patterns of disease progression and varied therapeutic responses. This review explores the evolution of breast cancer classifications, focusing on key prognostic and predictive factors. It examines traditional systems, such as the TNM staging and histological differentiation, while also incorporating modern elements like molecular subtypes, genomic alterations, and advanced diagnostic assays. By combining classical clinicopathological insights with cutting-edge molecular genetic technologies, the goal is to refine the precision of treatment strategies, ultimately advancing both our understanding and management of this complex disease. The review also emphasizes the importance of a global perspective, as achieving the primary treatment goals - prolonged survival and enhanced quality of life - requires addressing the disease in a broader, more comprehensive context. Breast cancer's complexity, driven by significant variability both across and within tumors, presents major challenges to conventional diagnostic and therapeutic approaches. However, breakthroughs in genomic research, such as molecular profiling and genetic testing, have deepened our understanding of this cancer's intricate nature. These advances have led to the identification of critical genetic alterations - including mutations in BRCA1/2, TP53, PALB2, PTEN, and PIK3CA - that profoundly impact tumor behavior, treatment efficacy, and patient prognosis. Genomic assays like Oncotype DX, MammaPrint, PROSIGNA, and EndoPredict offer valuable insights into recurrence risks and treatment choices, underscoring the growing importance of precision medicine. Moreover, the implementation of Molecular Tumor Boards further enhances personalized treatment strategies, contributing to improved patient outcomes and survival rates. This review underscores the significance of tailored therapeutic approaches and highlights the dynamic evolution of breast cancer in clinical practice.

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来源期刊
Chirurgia
Chirurgia Medicine-Surgery
CiteScore
1.00
自引率
0.00%
发文量
75
审稿时长
4-8 weeks
期刊介绍: Chirurgia is a bimonthly journal. In Chirurgia, original papers in the area of general surgery which neither appeared, nor were sent for publication in other periodicals, can be published. You can send original articles, new surgical techniques, or comprehensive general reports on surgical topics, clinical case presentations and, depending on publication space, - reviews of some articles of general interest to surgeons from other publications. Chirurgia is also a place for sharing information about the activity of various branches of the Romanian Society of Surgery, information on Congresses and Symposiums organized by the Romanian Society of Surgery and participation notes in other scientific meetings. Letters to the editor: Letters commenting on papers published in Chirurgia are welcomed. They should contain substantive ideas and commentaries supported by appropriate data, and should not exceed 2 pages. Please submit these letters to the editor through our online system.
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