Caparica Rafael, Lambertini Matteo, de Azambuja Evandro
Department of Medical Oncology, Institut Jules Bordet, Bruxelles, Belgium.
Department of Medical Oncology, UOC Clinica di Oncologia Medica, Ospedale Policlinico San Martino, Genova, Italy; Department of Internal Medicine and Medical Specialties (DiMI), School of Medicine, University of Genova, Genova, Italy.
ESMO Open. 2019 May 13;4(Suppl 2):e000504. doi: 10.1136/esmoopen-2019-000504. eCollection 2019.
Triple-negative breast cancer (TNBC) is associated with a high risk of recurrence and generally a bad prognosis. More than one-third of patients with TNBC will present distant metastases during the course of their disease. Although chemotherapy has been the main treatment option for metastatic TNBC for a long time, this scenario has changed recently with the advent of the polyadenosine diphosphate-ribose polymerase inhibitors (PARPis) for patients harbouring a mutation in the genes (BRCAmut) and also with the results of immunotherapy in patients with PD-L1-positive tumours. The present manuscript proposes a treatment algorithm for patients with metastatic TNBC based on the currently available, most relevant literature on the topic. For patients with a BRCAmut and able to tolerate chemotherapy, we recommend initiating treatment with platins (carboplatin/cisplatin) and to start PARPis at disease progression. For patients with PD-L1-positive tumours (PD-L1 expression on tumour-infiltrating immune cells ≥1%), we recommend first-line treatment with nab-paclitaxel and atezolizumab, when available. In patients without a mutation and with PD-L1-negative tumours, we recommend single-agent chemotherapy with taxanes (paclitaxel or docetaxel) as a first-line treatment. In patients with a high disease burden or who are very symptomatic, combinations such as anthracyclines plus cyclophosphamide or platins with taxanes are valid options. Chemotherapy should be maintained until the occurrence of disease progression or limiting toxicities. After progression to first-line chemotherapy, anthracyclines are an option for patients who received taxanes and vice versa. For patients who progressed to taxanes and anthracyclines, or who present contraindications to these agents, fluorouracil/capecitabine, eribulin, gemcitabine, cisplatin/carboplatin, vinorelbine and ixabepilone are alternatives. The treatment of TNBC is constantly evolving, and the inclusion of patients in ongoing trials evaluating new targeted agents, immunotherapy and predictive biomarkers should be encouraged, in an attempt to improve metastatic TNBC treatment outcomes.
三阴性乳腺癌(TNBC)与高复发风险相关,总体预后通常较差。超过三分之一的TNBC患者在病程中会出现远处转移。尽管长期以来化疗一直是转移性TNBC的主要治疗选择,但随着聚腺苷二磷酸核糖聚合酶抑制剂(PARPis)用于携带基因(BRCAmut)突变的患者以及PD-L1阳性肿瘤患者免疫治疗结果的出现,这种情况最近发生了变化。本手稿基于该主题目前可得的、最相关的文献,为转移性TNBC患者提出了一种治疗算法。对于有BRCAmut且能够耐受化疗的患者,我们建议开始使用铂类药物(卡铂/顺铂)治疗,并在疾病进展时开始使用PARPis。对于PD-L1阳性肿瘤患者(肿瘤浸润免疫细胞上的PD-L1表达≥1%),如有条件,我们建议一线治疗使用白蛋白结合型紫杉醇和阿特珠单抗。对于没有突变且PD-L1阴性肿瘤的患者,我们建议一线治疗使用紫杉烷类单药化疗(紫杉醇或多西他赛)。对于疾病负担高或症状非常明显的患者,蒽环类药物加环磷酰胺或铂类药物与紫杉烷类药物的联合方案也是有效的选择。化疗应持续至疾病进展或出现限制毒性。一线化疗进展后,对于接受过紫杉烷类药物治疗的患者,蒽环类药物是一种选择,反之亦然。对于进展至紫杉烷类药物和蒽环类药物治疗的患者,或对这些药物存在禁忌证的患者,氟尿嘧啶/卡培他滨、艾瑞布林、吉西他滨、顺铂/卡铂、长春瑞滨和伊沙匹隆是替代药物。TNBC的治疗在不断发展,应鼓励将患者纳入正在进行的评估新靶向药物、免疫治疗和预测生物标志物的试验,以试图改善转移性TNBC的治疗结果。