Suppr超能文献

曲妥珠单抗联合帕妥珠单抗与标准新辅助含蒽环类和不含蒽环类化疗方案联合用于人表皮生长因子受体 2 阳性早期乳腺癌患者:一项随机 II 期心脏安全性研究(TRYPHAENA)。

Pertuzumab plus trastuzumab in combination with standard neoadjuvant anthracycline-containing and anthracycline-free chemotherapy regimens in patients with HER2-positive early breast cancer: a randomized phase II cardiac safety study (TRYPHAENA).

机构信息

National Center for Tumor Diseases, University Hospital, Heidelberg, Germany.

出版信息

Ann Oncol. 2013 Sep;24(9):2278-84. doi: 10.1093/annonc/mdt182. Epub 2013 May 22.

Abstract

BACKGROUND

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.

PATIENTS AND METHODS

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.

RESULTS

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.

CONCLUSION

The combination of P with H and standard chemotherapy resulted in low rates of symptomatic LVSD.

摘要

背景

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。

患者和方法

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。

结果

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)。

结论

P 联合 H 和标准化疗导致有症状的 LVSD 发生率较低。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验