Pathological response and safety of albumin-bound paclitaxel as a neoadjuvant treatment for HER2-positive breast cancer compared to docetaxel combined with anti-HER2 therapy: a real-world study.

IF 3.5 3区 医学 Q2 ONCOLOGY Frontiers in Oncology Pub Date : 2024-08-21 eCollection Date: 2024-01-01 DOI:10.3389/fonc.2024.1412051
Zhidong Lyu, Linlin Gao
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Abstract

Background: This study aimed to retrospectively analyse the pathological response and safety of combining albumin-bound paclitaxel (nab-paclitaxel) or docetaxel with anti-HER2 therapy as a neoadjuvant treatment for HER2-positive breast cancer.

Methods: From June 2020 to August 2023, 225 HER2-positive breast cancer patients who underwent radical surgery following neoadjuvant treatment were enrolled in this study. The patients were divided into two groups based on the drugs they received: the nab-paclitaxel group (n=166, receiving nab-paclitaxel + platinum along with trastuzumab and pertuzumab) and the docetaxel group (n=59, receiving docetaxel + platinum along with trastuzumab and pertuzumab). The pathological response and adverse events related to the drugs were collected and evaluated in both groups.

Results: In the nab-paclitaxel group, the rates of breast and total pathological complete response (bpCR and tpCR) were significantly greater than those in the docetaxel group (69.27% vs. 47.45%, P=0.003; 68.67% vs. 45.76%, P=0.002). For patients who did not achieve pCR after chemotherapy, the pathological response of chemotherapy was analysed using MP grading and RCB grading. The results showed that there was a statistically significant difference between the two groups (P<0.05). Multivariate analysis revealed that therapeutic drugs, clinical stage, ER status, and Ki-67 level were independent predictors of pCR. The nab-paclitaxel group had a significantly greater proportion of patients with peripheral sensory neuropathy than did the docetaxel group (58.43% vs. 38.98%, P=0.035), while the docetaxel group had a greater proportion of patients with allergies and elevated ALT (31.93% vs. 69.49%, P=0.000; 23.49% vs. 40.68%, P=0.021).

Conclusions: Our real-world study revealed that nab-paclitaxel combined with anti-HER2 therapy was an effective neoadjuvant therapy for HER2-positive breast cancer. The multivariate analysis revealed that chemotherapy drugs, clinical stage, ER status, and Ki-67 level was the significant factor influencing treatment outcome. These findings offer a valuable reference for the neoadjuvant treatment of patients with HER2-positive breast cancer.

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白蛋白结合紫杉醇作为HER2阳性乳腺癌新辅助治疗与多西他赛联合抗HER2治疗的病理反应和安全性比较:一项真实世界研究。
研究背景本研究旨在回顾性分析白蛋白结合型紫杉醇(nab-紫杉醇)或多西他赛联合抗HER2治疗作为HER2阳性乳腺癌新辅助治疗的病理反应和安全性:2020年6月至2023年8月,225名HER2阳性乳腺癌患者在新辅助治疗后接受了根治性手术。根据患者接受的药物分为两组:纳伯紫杉醇组(n=166,接受纳伯紫杉醇+铂金以及曲妥珠单抗和百妥珠单抗)和多西他赛组(n=59,接受多西他赛+铂金以及曲妥珠单抗和百妥珠单抗)。收集并评估了两组患者的病理反应和与药物相关的不良反应:纳布-紫杉醇组的乳腺癌和总病理完全反应率(bpCR 和 tpCR)明显高于多西他赛组(69.27% vs. 47.45%,P=0.003;68.67% vs. 45.76%,P=0.002)。对于化疗后未达到pCR的患者,采用MP分级和RCB分级分析化疗的病理反应。结果显示,两组之间存在显著的统计学差异(PConclusions:我们的真实世界研究显示,纳布-紫杉醇联合抗HER2疗法是治疗HER2阳性乳腺癌的有效新辅助疗法。多变量分析显示,化疗药物、临床分期、ER状态和Ki-67水平是影响治疗结果的重要因素。这些研究结果为HER2阳性乳腺癌患者的新辅助治疗提供了有价值的参考。
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来源期刊
Frontiers in Oncology
Frontiers in Oncology Biochemistry, Genetics and Molecular Biology-Cancer Research
CiteScore
6.20
自引率
10.60%
发文量
6641
审稿时长
14 weeks
期刊介绍: Cancer Imaging and Diagnosis is dedicated to the publication of results from clinical and research studies applied to cancer diagnosis and treatment. The section aims to publish studies from the entire field of cancer imaging: results from routine use of clinical imaging in both radiology and nuclear medicine, results from clinical trials, experimental molecular imaging in humans and small animals, research on new contrast agents in CT, MRI, ultrasound, publication of new technical applications and processing algorithms to improve the standardization of quantitative imaging and image guided interventions for the diagnosis and treatment of cancer.
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