Pyrotinib and Trastuzumab Plus Chemotherapy Serve as an Acceptable Neoadjuvant Regimen Exhibiting Good Efficacy and Tolerance in HER2-Positive Breast Cancer Patients.

IF 2.4 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Cancer Biotherapy and Radiopharmaceuticals Pub Date : 2024-08-01 Epub Date: 2024-03-25 DOI:10.1089/cbr.2023.0175
Yibo Chen, Tianyi Zhang, Rui Zhang, Xuchen Cao
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引用次数: 0

Abstract

Objective: Pyrotinib, a new irreversible dual pan-human epidermal growth factor receptor 2 (HER2) receptor tyrosine kinase inhibitor blocking EGFR and HER2, has achieved a promising efficacy for advanced HER2-positive (HER2+) breast cancer. This study intended to further investigate the efficacy and safety of neoadjuvant pyrotinib and trastuzumab plus chemotherapy for HER2+ breast cancer treatment. Methods: Thirty-eight HER2+ breast cancer patients who received neoadjuvant pyrotinib and trastuzumab plus chemotherapy (docetaxel and carboplatin) were retrospectively reviewed. Clinical response by Response Evaluation Criteria in Solid Tumors (RECIST), pathological complete response (pCR), and adverse events data was retrieved. Results: According to the RECIST, the complete response rate was 0.0%, 10.5%, and 15.8% after second-cycle, fourth-cycle, and sixth-cycle therapy, respectively; whereas the objective response rate was 76.3%, 92.1%, and 100.0%, accordingly. The total pCR (tpCR) rate was 52.6%, the pCR rate of the breast was also 52.6%, and the pCR rate of lymph nodes was 86.8%. The tpCR rate was lower in patients with HER2 immunohistochemistry (IHC)++ and amplification by fluorescent in situ hybridization (FISH) than in those with HER2 IHC+++ (14.3% vs. 61.3%, p = 0.024), which was also lower in patients with Ki-67 expression ≥30% than in those with Ki-67 expression <30% (40.0% vs. 76.9%, p = 0.031). The common adverse events included diarrhea (84.2%), anemia (73.7%), nausea and vomiting (63.2%), fatigue (50.0%), hypomagnesemia (44.7%), leukopenia (42.1%), thrombocytopenia (39.5%), elevated transaminase (36.8%), and pruritus (31.6%). Conclusions: Pyrotinib and trastuzumab plus chemotherapy serve as an acceptable neoadjuvant regimen exhibiting good efficacy and tolerance in HER2+ breast cancer patients, while further large-scale validation is warranted.

派罗替尼和曲妥珠单抗加化疗是一种可接受的新辅助治疗方案,对HER2阳性乳腺癌患者具有良好的疗效和耐受性。
研究目的派罗替尼是一种新型不可逆的双泛人表皮生长因子受体2(HER2)受体酪氨酸激酶抑制剂,可阻断表皮生长因子受体(EGFR)和HER2,对晚期HER2阳性(HER2+)乳腺癌具有良好疗效。本研究旨在进一步探讨新辅助派罗替尼和曲妥珠单抗联合化疗治疗HER2+乳腺癌的有效性和安全性。研究方法回顾性分析38例HER2+乳腺癌患者,这些患者接受了新辅助派罗替尼和曲妥珠单抗联合化疗(多西他赛和卡铂)。根据实体瘤反应评估标准(RECIST)检索了临床反应、病理完全反应(pCR)和不良反应数据。结果:根据RECIST标准,第二周期、第四周期和第六周期治疗后的完全反应率分别为0.0%、10.5%和15.8%,而客观反应率分别为76.3%、92.1%和100.0%。总的 pCR(tpCR)率为 52.6%,乳腺的 pCR 率也是 52.6%,淋巴结的 pCR 率为 86.8%。HER2免疫组化(IHC)+++和荧光原位杂交(FISH)扩增的患者的tpCR率低于HER2 IHC+++的患者(14.3% vs. 61.3%,p = 0.024),Ki-67表达≥30%的患者的tpCR率也低于Ki-67表达≥30%的患者(p = 0.031)。常见的不良反应包括腹泻(84.2%)、贫血(73.7%)、恶心和呕吐(63.2%)、疲劳(50.0%)、低镁血症(44.7%)、白细胞减少(42.1%)、血小板减少(39.5%)、转氨酶升高(36.8%)和瘙痒(31.6%)。结论派罗替尼和曲妥珠单抗联合化疗是一种可接受的新辅助治疗方案,对HER2+乳腺癌患者具有良好的疗效和耐受性,但还需要进一步的大规模验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.80
自引率
2.90%
发文量
87
审稿时长
3 months
期刊介绍: Cancer Biotherapy and Radiopharmaceuticals is the established peer-reviewed journal, with over 25 years of cutting-edge content on innovative therapeutic investigations to ultimately improve cancer management. It is the only journal with the specific focus of cancer biotherapy and is inclusive of monoclonal antibodies, cytokine therapy, cancer gene therapy, cell-based therapies, and other forms of immunotherapies. The Journal includes extensive reporting on advancements in radioimmunotherapy, and the use of radiopharmaceuticals and radiolabeled peptides for the development of new cancer treatments.
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