Jacobs Flavia, Agostinetto Elisa, Miggiano Chiara, De Sanctis Rita, Zambelli Alberto, Santoro Armando
Department of Biomedical Sciences, Humanitas University, Via Rita Levi Montalcini 4, 20090 Pieve Emanuele, MI, Italy.
Academic Trials Promoting Team, Institut Jules Bordet, L'Université Libre de Bruxelles (U.L.B.), 1070 Brussels, Belgium.
Cancers (Basel). 2023 May 26;15(11):2933. doi: 10.3390/cancers15112933.
Triple-negative breast cancer (TNBC) holds a poor prognosis compared to other breast cancer subtypes, and the development of new effective treatment strategies is an unmet medical need. TNBC has traditionally been considered not amenable to treatment with targeted agents due to a lack of actionable targets. Therefore, chemotherapy has remained the mainstay of systemic treatment for many decades. The advent of immunotherapy raised very hopeful expectations in TNBC, possibly due to higher levels of tumor-infiltrating lymphocytes, PD-L1 expression and tumor mutational burden compared to other breast cancer subtypes, that predict an effective anti-tumor immune-engagement. The results of clinical trials testing immunotherapy in TNBC led to the approval of the combination of immune checkpoint inhibitors and chemotherapy in both early and advanced settings. However, some open questions about the use of immunotherapy in TNBC still exist. These include a deeper understanding of the heterogeneity of the disease, identification of reliable predictive biomarkers of response, determination of the most appropriate chemotherapy backbone and appropriate management of potential long-term immune-related adverse events. In this review we aim to examine the available evidence on the use of immunotherapy strategies in both early and advanced TNBC, to critically discuss some of the limitations encountered in clinical research and to summarize data on novel promising immunotherapeutic strategies beyond PD-(L)1 blockade that have been investigated in the most recent trials.
与其他乳腺癌亚型相比,三阴性乳腺癌(TNBC)的预后较差,开发新的有效治疗策略是尚未满足的医学需求。传统上,由于缺乏可操作的靶点,TNBC被认为不适合使用靶向药物治疗。因此,几十年来化疗一直是全身治疗的主要手段。免疫疗法的出现给TNBC带来了很大希望,这可能是因为与其他乳腺癌亚型相比,TNBC的肿瘤浸润淋巴细胞水平更高、PD-L1表达和肿瘤突变负荷更高,这些因素预示着有效的抗肿瘤免疫反应。在TNBC中测试免疫疗法的临床试验结果导致免疫检查点抑制剂与化疗的联合方案在早期和晚期治疗中均获得批准。然而,关于TNBC中免疫疗法的使用仍存在一些未解决的问题。这些问题包括更深入地了解该疾病的异质性、识别可靠的反应预测生物标志物、确定最合适的化疗方案以及对潜在的长期免疫相关不良事件进行适当管理。在本综述中,我们旨在研究早期和晚期TNBC中使用免疫疗法策略的现有证据,批判性地讨论临床研究中遇到的一些局限性,并总结最近试验中研究的除PD-(L)1阻断之外的有前景的新型免疫治疗策略的数据。