双重抗her2治疗与单曲妥珠单抗联合新辅助蒽环类和紫杉烷治疗her2阳性早期乳腺癌:现实世界的见解

IF 5.3 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Biologics : Targets & Therapy Pub Date : 2025-03-05 eCollection Date: 2025-01-01 DOI:10.2147/BTT.S468650
Baha Sharaf, Faris Tamimi, Haneen Al-Abdallat, Suhaib Khater, Osama Salama, Anas Zayed, Osama El Khatib, Assem Qaddoumi, Malek Horani, Yosra Al-Masri, Wafa Asha, Bayan Altalla', Hira Bani Hani, Hikmat Abdel-Razeq
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引用次数: 0

摘要

在her2阳性早期乳腺癌(EBC)患者中,抗her2靶向治疗与化疗的结合已经证明了病理完全缓解率(pCR)的增加。本研究提供了曲妥珠单抗联合或不联合帕妥珠单抗,与蒽环类和紫杉烷类化疗方案联合使用的真实数据。方法:我们对2014年1月至2021年9月期间接受新辅助化疗(NACT)治疗的her2阳性EBC患者进行了回顾性分析。该方案包括4个周期的阿霉素和环磷酰胺(AC),随后每3周4个周期的多西他赛,抗her2治疗与多西他赛同时进行。评估的结果包括pCR、3年无病生存(DFS)和手术结果。结果:在研究期间,纳入了484例her2阳性EBC患者,中位年龄为47岁(范围21-80岁)。64.7%的患者接受了双重抗her2治疗,35.3%的患者接受了单药曲妥珠单抗治疗。总pCR率为44.2%,其中激素受体(HR)阴性患者的pCR率(55.6%)高于HR阳性患者(39.8%),p=0.002。虽然双药治疗的pCR率(46.6%)高于单药曲妥珠单抗(39.8%),但差异无统计学意义(p=0.15)。双药治疗的3年DFS为86.1%,单曲妥珠单抗治疗的3年DFS为83.1% (p=0.37)。进一步分层显示,淋巴结阴性疾病的3年DFS(96.4%)优于淋巴结阳性疾病(82.3%),p=0.0021。实现pCR的患者3年DFS(89.3%)明显优于残留疾病患者(82.2%),p=0.0177。单独接受曲妥珠单抗治疗的患者保乳手术(BCS)率较低(15.2%),而双抗her2治疗的患者为26.5%[优势比(OR)= 0.50, 95%可信区间(CI), 0.30-0.80, p=0.005]。结论:双重抗her2治疗并未显著提高DFS,但与更高的BCS发生率相关,突出了其改善手术结果的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dual Anti-HER2 Therapy Vs Trastuzumab Alone with Neoadjuvant Anthracycline and Taxane in HER2-Positive Early-Stage Breast Cancer: Real-World Insights.

Introduction: The integration of anti-HER2 targeted therapy with chemotherapy has demonstrated an increase in pathologic complete response rates (pCR) in patients with HER2-positive early-stage breast cancer (EBC). This study presents real-world data on the use of trastuzumab with or without pertuzumab, in combination with anthracycline and taxanes-based chemotherapy regimen.

Methods: We conducted a retrospective analysis of patients with HER2-positive EBC who underwent neoadjuvant chemotherapy (NACT), treated between January 2014 and September 2021. The regimen included four cycles of doxorubicin and cyclophosphamide (AC), followed by four cycles of docetaxel every three weeks, with anti-HER2 therapy administered alongside docetaxel. Outcomes assessed included pCR, 3-year disease-free survival (DFS), and surgical outcomes.

Results: During the study period, 484 consecutive patients with HER2-positive EBC, median age of 47 (range, 21-80) years, were enrolled. (64.7%) of patients received dual anti-HER2 therapy, while 35.3% received single-agent trastuzumab. The overall pCR rate was 44.2%, with a higher rate (55.6%) in hormone receptor (HR)-negative patients compared to HR-positive patients (39.8%), p=0.002. Although dual therapy resulted in a higher pCR rate (46.6%) compared to trastuzumab alone (39.8%), the difference was not statistically significant (p=0.15). The estimated 3-year DFS was 86.1% with dual therapy and 83.1% with trastuzumab alone (p=0.37). Further stratification revealed superior 3-year DFS in node-negative disease (96.4%) compared to node-positive disease (82.3%), p=0.0021. Patients who achieved pCR had a significantly better 3-year DFS (89.3%) compared to those with residual disease (82.2%), p=0.0177. Rate of breast conserving surgery (BCS) was lower (15.2%) among patients who received trastuzumab alone, compared to 26.5% among those who received dual anti-HER2 [Odds Ratio (OR)= 0.50, 95% Confidence Interval (CI), 0.30-0.80, p=0.005].

Conclusion: Dual anti-HER2 therapy did not significantly enhance DFS but was associated with higher BCS rates, highlighting its potential to improve surgical outcomes.

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来源期刊
Biologics : Targets & Therapy
Biologics : Targets & Therapy MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
8.30
自引率
0.00%
发文量
22
审稿时长
16 weeks
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