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激素受体阳性、HER2阴性乳腺癌新辅助化疗的当前文献及真实世界结果综述

A Review of Current Literature and Real-World Outcomes With Neoadjuvant Chemotherapy in Hormone Receptor Positive, HER2 Negative Breast Cancer.

作者信息

Guzik Gregory, Kurian Matthew, Patell Kanchi, Trybula Marcus, Fu Pingfu, Margevicius Seunghee, Montero Alberto, Martin James

机构信息

University Hospitals, Cleveland, OH.

St. Elizabeth Healthcare, Edgewood, KY.

出版信息

Clin Breast Cancer. 2025 Jul;25(5):e666-e677. doi: 10.1016/j.clbc.2025.03.008. Epub 2025 Mar 12.

Abstract

BACKGROUND

Neoadjuvant chemotherapy has been used to downstage locally advanced ER+/HER2- breast cancer with low response rates. The optimal neoadjuvant regimen for this population is unknown.

PATIENTS AND METHODS

Between 2017 and 2022, 192 patients (ages 28-78) with stage II/III ER+/Her2- breast cancer at our institution were evaluated. Patients were divided into 4 groups based on the neoadjuvant chemotherapy regimen used (AC-T, TC, TAC, or other). The responses were categorized as complete (ypT0/is ypN0), partial, no response, or progressive disease.

RESULTS

The choice of neoadjuvant chemotherapy was not predictive of pCR (P = .3864), even among those with more advanced nodal disease. No significant difference was noted in OS or IDFS at 24 or 48 months between the AC-T and TC groups. In the AC-T group (n = 130), 9 patients had a CR (6.98%), while no patients in TC group had a CR. Those who were premenopausal were more likely to achieve pCR compared to those postmenopausal. Race significantly impacted IDFS.

CONCLUSIONS

In this single center study, we found no differences in IDFS or OS when comparing neoadjuvant TC to AC-T. The AC-T regimen group had a higher pCR rate of 6.98% compared to 0% in TC regimen group. Further exploration is needed to understand why non-white populations have inferior IDFS.

摘要

背景

新辅助化疗已被用于降低局部晚期雌激素受体阳性/人表皮生长因子受体2阴性乳腺癌的分期,但缓解率较低。该人群的最佳新辅助治疗方案尚不清楚。

患者与方法

2017年至2022年期间,对我院192例年龄在28 - 78岁的II/III期雌激素受体阳性/人表皮生长因子受体2阴性乳腺癌患者进行了评估。根据所使用的新辅助化疗方案(AC-T、TC、TAC或其他)将患者分为4组。反应分为完全缓解(ypT0/is ypN0)、部分缓解、无反应或疾病进展。

结果

新辅助化疗方案的选择并不能预测病理完全缓解(P = 0.3864),即使在那些有更晚期淋巴结疾病的患者中也是如此。AC-T组和TC组在24个月或48个月时的总生存期(OS)或无病间期(IDFS)没有显著差异。在AC-T组(n = 130)中,9例患者达到完全缓解(6.98%),而TC组没有患者达到完全缓解。与绝经后患者相比,绝经前患者更有可能实现病理完全缓解。种族对无病间期有显著影响。

结论

在这项单中心研究中,我们发现新辅助TC方案与AC-T方案相比,在无病间期或总生存期方面没有差异。AC-T方案组的病理完全缓解率为6.98%,高于TC方案组的0%。需要进一步探索以了解为什么非白人人群的无病间期较差。

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