National Center for Tumor Diseases, University Hospital, Heidelberg, Germany.
Ann Oncol. 2013 Sep;24(9):2278-84. doi: 10.1093/annonc/mdt182. Epub 2013 May 22.
Pertuzumab (P) combined with trastuzumab (H)-based chemotherapy improves efficacy in early and advanced HER2-positive breast cancer. We assessed the tolerability, with particular focus on cardiac safety, of H and P with chemotherapy in the neoadjuvant treatment of HER2-positive early breast cancer.
In this multicenter, open-label phase II study, patients with operable, locally advanced, or inflammatory breast cancer were randomized 1 : 1 : 1 to receive six neoadjuvant cycles q3w (Arm A: 5-fluorouracil, epirubicin, cyclophosphamide [FEC] + H + P ×3 → docetaxel [T] + H + P ×3; Arm B: FEC ×3 → T + H + P ×3; Arm C: T + carboplatin + H [TCH]+P ×6). pCR was assessed at surgery and adjuvant therapy given to complete 1 year of H.
Two hundred twenty-five patients were randomized. During neoadjuvant treatment, two patients (2.7%; Arm B) experienced symptomatic left ventricular systolic dysfunction (LVSD) and 11 patients (Arm A: 4 [5.6%]; Arm B: 4 [5.3%]; Arm C: 3 [3.9%]) had declines in left ventricular ejection fraction of ≥10% points from baseline to <50%. Diarrhea was the most common adverse event. pCR (ypT0/is) was reported for 61.6% (Arm A), 57.3% (Arm B), and 66.2% (Arm C) of patients.
The combination of P with H and standard chemotherapy resulted in low rates of symptomatic LVSD.
帕妥珠单抗(P)联合曲妥珠单抗(H)为基础的化疗可提高早期和晚期 HER2 阳性乳腺癌的疗效。我们评估了 H 和 P 联合化疗在 HER2 阳性早期乳腺癌新辅助治疗中的耐受性,特别关注心脏安全性。
在这项多中心、开放标签的 II 期研究中,将可手术的局部晚期或炎性乳腺癌患者按 1:1:1 随机分为三组,分别接受六周期新辅助治疗,每 3 周 1 次(A 组:5-氟尿嘧啶、表柔比星、环磷酰胺[FEC]+H+P×3→多西他赛[T]+H+P×3;B 组:FEC×3→T+H+P×3;C 组:T+卡铂+H[TCH]+P×6)。手术时评估 pCR,并给予辅助治疗以完成 1 年 H 治疗。
共 225 例患者随机分组。在新辅助治疗期间,2 例患者(2.7%;B 组)出现有症状的左心室收缩功能障碍(LVSD),11 例患者(A 组:4[5.6%];B 组:4[5.3%];C 组:3[3.9%])左心室射血分数从基线下降≥10%,至<50%。腹泻是最常见的不良事件。pCR(ypT0/is)报告率为 61.6%(A 组)、57.3%(B 组)和 66.2%(C 组)。
P 联合 H 和标准化疗导致有症状的 LVSD 发生率较低。