Pertuzumab in Combination with Trastuzumab and Docetaxel in the Neoadjuvant Treatment for HER2-Positive Breast Cancer.

Q3 Medicine
Cláudia Vieira, Andreia Borges, Filipa F Pereira, Pedro Antunes, Patrícia Redondo, Luís Antunes, José M Lopes, Francisco R Gonçalves, Marina Borges, Maria J Bento
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Abstract

Introduction: This study aims to assess safety and effectiveness of pertuzumab in combination with trastuzumab and docetaxel in the neoadjuvant treatment (NeoT) of HER2-positive breast cancer.

Methods: Two consecutive retrospective cohorts (n = 94, 2012-2015 and 2015-2017) of adult women with HER2-positive breast cancer, receiving NeoT at the breast clinic in Portugal (IPO-Porto), were followed. All patients had surgery and received trastuzumab as adjuvant therapy. The 2012-2015 cohort received doxorubicin, cyclophosphamide, docetaxel plus trastuzumab, whereas the 2015-2017 cohort was treated with the same protocol plus pertuzumab.

Results: The 2012-2015 cohort was older (median 53 years), with locally advanced tumors (48.1%), mostly hormone receptor positive (59.3%). The 2015-2017 cohort was younger (median 43 years) with 60% operable tumors. Pathologic complete response (pCR) improved in the second cohort, while maintaining a good safety profile and tolerability. Clinical staging (p = 0.001) and hormone receptor (p = 0.003) were significant predictors of pCR, but not treatment regimen (p = 0.304).

Conclusion: Further research with larger samples and longer follow-up is needed to understand the clinical differences. Clinical effectiveness of treatment should also be measured through overall and progression-free survival.

Abstract Image

Abstract Image

帕妥珠单抗联合曲妥珠单抗和多西紫杉醇治疗her2阳性乳腺癌的新辅助治疗
简介:本研究旨在评估帕妥珠单抗联合曲妥珠单抗和多西他赛在her2阳性乳腺癌新辅助治疗(NeoT)中的安全性和有效性。方法:连续两组回顾性队列(n = 94, 2012-2015年和2015-2017年),在葡萄牙(IPO-Porto)乳腺诊所接受NeoT治疗的her2阳性乳腺癌成年女性。所有患者均接受手术并接受曲妥珠单抗辅助治疗。2012-2015年队列接受阿霉素、环磷酰胺、多西他赛加曲妥珠单抗治疗,而2015-2017年队列接受相同方案加帕妥珠单抗治疗。结果:2012-2015年队列年龄较大(中位53岁),局部肿瘤晚期(48.1%),大多数激素受体阳性(59.3%)。2015-2017年的队列更年轻(中位年龄43岁),60%的肿瘤可手术。病理完全缓解(pCR)在第二队列中得到改善,同时保持良好的安全性和耐受性。临床分期(p = 0.001)和激素受体(p = 0.003)是pCR的显著预测因子,而治疗方案不是(p = 0.304)。结论:进一步的研究需要更大的样本和更长时间的随访来了解临床差异。治疗的临床有效性也应通过总生存期和无进展生存期来衡量。
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来源期刊
CiteScore
2.40
自引率
0.00%
发文量
17
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