Breast Cancer Unit, Vall d'Hebrón Institute of Oncology, Barcelona, Spain.
Fortrea, Inc., Durham, USA; Addenbrooke's Hospital, Cambridge University Hospitals National Health Service (NHS) Foundation Trust, Cambridge, UK.
ESMO Open. 2024 Oct;9(10):103713. doi: 10.1016/j.esmoop.2024.103713. Epub 2024 Oct 1.
Patients with triple-negative breast cancer (TNBC) have a relatively poor clinical outcome. The immune checkpoint inhibitor (ICI) pembrolizumab combined with chemotherapy is the current standard of care in TNBC patients with stage II and III. Monotherapy with ICIs has not been comprehensively assessed in the neoadjuvant setting in TNBC patients, given unfavorable results in metastatic trials. ICIs, however, have been tested in the window of opportunity (WOO) before surgery or standard chemotherapy-based neoadjuvant treatment. The WOO design is well suited to assess an ICI alone or in combination with other ICIs, targeted therapy, radiotherapy or cryotherapy, and measure their pharmacodynamic and clinical effect in this treatment-naive population. Some patients show a good response to ICIs in WOO studies. Biomarkers like tumor-infiltrating lymphocytes, programmed death ligand-1, and interferon-γ signature may predict activity and may identify patients likely to benefit from ICIs. Moreover, an increase in tumor-infiltrating lymphocytes, programmed death ligand-1 expression or T cell receptor expansion following administration of ICIs in the WOO setting could potentially inform of immunotherapy benefit, which would allow tailoring further treatment. This article reviews WOO trials that assessed immunotherapy in the early-stage TNBC population, and how these results could be translated to test de-escalation strategies of neoadjuvant chemotherapy and immunotherapy without compromising a patient's prognosis.
三阴性乳腺癌 (TNBC) 患者的临床预后相对较差。免疫检查点抑制剂 (ICI) 帕博利珠单抗联合化疗是目前 II 期和 III 期 TNBC 患者的标准治疗方法。鉴于转移性试验的不利结果,ICI 单药治疗在 TNBC 患者的新辅助治疗中尚未得到全面评估。然而,ICI 已在手术前或基于标准化疗的新辅助治疗的机会之窗 (WOO) 中进行了测试。WOO 设计非常适合评估 ICI 单独或与其他 ICI、靶向治疗、放疗或冷冻治疗联合使用,并在这种未经治疗的人群中测量它们的药效学和临床效果。一些患者在 WOO 研究中对 ICI 有很好的反应。生物标志物,如肿瘤浸润淋巴细胞、程序性死亡配体-1 和干扰素-γ 特征,可能预测活性,并可能识别出可能受益于 ICI 的患者。此外,在 WOO 中,ICI 给药后肿瘤浸润淋巴细胞、程序性死亡配体-1 表达或 T 细胞受体扩增的增加可能提示免疫治疗获益,这将允许进一步治疗的个体化。本文综述了评估早期 TNBC 人群免疫治疗的 WOO 试验,以及如何将这些结果转化为测试新辅助化疗和免疫治疗的降级策略,而不影响患者的预后。