Department of Internal Medicine, King Hussein Cancer Center, Amman 11941, Jordan.
School of Medicine, University of Jordan, Amman 11941, Jordan.
Curr Oncol. 2022 Aug 16;29(8):5810-5822. doi: 10.3390/curroncol29080458.
Breast cancer continues to be the most diagnosed cancer among women worldwide. Neoadjuvant chemotherapy is the standard of care for breast cancer patients with locally advanced disease and patients with poor pathological features, such as triple-negative (TN) or human epidermal growth factor receptor-2 (HER2)-positive subtypes. Neoadjuvant therapy offers several advantages, including better surgical outcomes, early systemic treatment for micro-metastases, and accurate tumor biology and chemosensitivity assessment. Multiple studies have shown that achieving pathological complete response (pCR) following neoadjuvant chemotherapy is associated with better prognosis and better treatment outcomes; almost half of such patients may fail to achieve pCR. Tumor proliferative index, hormone receptor (HR) status, and HER2 expression are the major predictors of pCR. Strategies to improve pCR have been dependent on augmenting neoadjuvant chemotherapy with the addition of taxanes and dual anti-HER2 targeted therapy in patients with HER2-positive tumor, and more recently, immunotherapy for patients with TN disease. The clinical management of patients with residual disease following neoadjuvant chemotherapy varies and depends mostly on the level of HR expression and HER2 status. Recent data have suggested that switching trastuzumab to trastuzumab-emtansine (T-DM1) in patients with HER2-positive disease and the addition of capecitabine for patients with HER2-negative and HR-negative subtype is associated with a better outcome; both strategies are incorporated into current clinical practice guidelines. This paper reviews available and ongoing studies addressing strategies to better manage patients who continue to have residual disease following neoadjuvant chemotherapy.
乳腺癌仍然是全球女性中最常见的诊断癌症。新辅助化疗是局部晚期乳腺癌患者和三阴性(TN)或人表皮生长因子受体-2(HER2)阳性亚型等病理特征不良患者的标准治疗方法。新辅助治疗有几个优点,包括更好的手术结果、对微转移的早期全身治疗以及准确的肿瘤生物学和化疗敏感性评估。多项研究表明,新辅助化疗后达到病理完全缓解(pCR)与更好的预后和更好的治疗结果相关;几乎一半的此类患者可能无法达到 pCR。肿瘤增殖指数、激素受体(HR)状态和 HER2 表达是 pCR 的主要预测因素。提高 pCR 的策略一直依赖于在 HR 阳性肿瘤患者中用紫杉烷和双重抗 HER2 靶向治疗增强新辅助化疗,最近,在 TN 疾病患者中使用免疫疗法。新辅助化疗后残留疾病患者的临床管理因 HR 表达和 HER2 状态而异。最近的数据表明,在 HER2 阳性疾病患者中,将曲妥珠单抗转换为曲妥珠单抗-美坦新(T-DM1),在 HER2 阴性和 HR 阴性亚型患者中加用卡培他滨与更好的结果相关;这两种策略都被纳入当前的临床实践指南。本文综述了目前正在进行的研究,旨在探讨更好地管理新辅助化疗后仍有残留疾病的患者的策略。