CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Immunotherapy in triple-negative breast cancer: Insights into tumor immune landscape and therapeutic opportunities.
Immunotherapy in triple-negative breast cancer: Insights into tumor immune landscape and therapeutic opportunities.
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三阴性乳腺癌(TNBC)是一种临床上具有侵袭性的乳腺癌亚型,占乳腺肿瘤的15-20%,在年轻绝经前女性中更为常见。它是乳腺癌中转移潜能最高、诊断后最初5年内复发率最高的亚型。
此外,当未达到完全病理缓解时,死亡率会增加。由于TNBC细胞缺乏雌激素、孕激素和HER2受体,患者对激素治疗和抗HER2治疗反应不佳,常规化疗仍是标准治疗。尽管在开发靶向治疗方面做出了努力,但该疾病仍有很高的未满足医疗需求,迫切需要个性化的诊断和治疗方案。随着免疫治疗正在改变抗癌治疗的范式,它成为TNBC患者的一种替代治疗选择。TNBC因其高水平的肿瘤突变负荷和免疫细胞浸润的存在,被归类为乳腺癌的免疫原性亚型。本综述探讨了这些特征对该疾病诊断、治疗和预后的意义。本文综述了免疫基因特征和TIL(肿瘤浸润淋巴细胞)作为TNBC生物标志物的作用,确定了它们在患者诊断和分层中的应用,以及作为疗效预测因子的价值。PD-L1的表达已被认为可预测对检查点抑制剂治疗的反应,但本文描述了其作为生物标志物所面临的挑战。
此外,讨论了目前正在临床研究中的针对TNBC的不同形式免疫治疗的理论依据,并重点介绍了主要临床试验。免疫检查点抑制剂已显示出临床获益,尤其是在早期肿瘤以及与化疗联合给药时,已有多种方案获得监管机构批准。抗体药物偶联物的成功以及其他新兴方法(如疫苗和细胞疗法)的研究也将被讨论。这些进展为开发个性化、更有效且安全的治疗带来了希望,这将改善TNBC患者的生存期和生活质量。
Triple-negative breast cancer (TNBC) is a clinically aggressive subtype of breast cancer that represents 15-20% of breast tumors and is more prevalent in young pre-menopausal women. It is the subtype of breast cancers with the highest metastatic potential and recurrence at the first 5 years after diagnosis.
In addition, mortality increases when a complete pathological response is not achieved. As TNBC cells lack estrogen, progesterone, and HER2 receptors, patients do not respond well to hormone and anti-HER2 therapies, and conventional chemotherapy remains the standard treatment. Despite efforts to develop targeted therapies, this disease continues to have a high unmet medical need, and there is an urgent demand for customized diagnosis and therapeutics.
As immunotherapy is changing the paradigm of anticancer treatment, it arises as an alternative treatment for TNBC patients. TNBC is classified as an immunogenic subtype of breast cancer due to its high levels of tumor mutational burden and presence of immune cell infiltrates. This review addresses the implications of these characteristics for the diagnosis, treatment, and prognosis of the disease.
Herein, the role of immune gene signatures and tumor-infiltrating lymphocytes as biomarkers in TNBC is reviewed, identifying their application in patient diagnosis and stratification, as well as predictors of efficacy. The expression of PD-L1 expression is already considered to be predictive of response to checkpoint inhibitor therapy, but the challenges regarding its value as biomarker are described.
Moreover, the rationales for different formats of immunotherapy against TNBC currently under clinical research are discussed, and major clinical trials are highlighted. Immune checkpoint inhibitors have demonstrated clinical benefit, particularly in early-stage tumors and when administered in combination with chemotherapy, with several regimens approved by the regulatory authorities.
The success of antibody-drug conjugates and research on other emerging approaches, such as vaccines and cell therapies, will also be addressed. These advances give hope on the development of personalized, more effective, and safe treatments, which will improve the survival and quality of life of patients with TNBC.
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