[Dose-dense paclitaxel plus carboplatin in combination with trastuzumab neoadjuvant versus standard adjuvant therapy in human epidermal growth factor receptor-2 positive and hormone receptor negative breast cancer: a prospective cohort study].

M Xiu, Y Lu, X Wang, Y Fan, Q Li, Q Li, J Y Wang, Y Luo, R G Cai, S S Chen, P Yuan, F Ma, B H Xu, P Zhang
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引用次数: 0

Abstract

Objective: To provide survival evidence of anthracycline-free neoadjuvant chemotherapy for patients with stages Ⅱ-Ⅲ human epidermal growth factor receptor-2 (HER-2) positive and hormone receptor (HR) negative breast cancer. Methods: The prospective cohort study was conducted at the Department of Medical Oncology of Cancer Hospital, Chinese Academy of Medical Sciences. Patients with HER-2 positive and HR negative breast cancer in stages Ⅱ-Ⅲ were enrolled to receive neoadjuvant therapy (NAT) of dose-dense paclitaxel (175 mg/m(2)) plus carboplatin (AUC=4.0) biweekly for 6 cycles in combination with trastuzumab (PCbH), and matched patients who received standard adjuvant therapy of physicians' choice were recruited for survival and safety comparison. Results: From July 2013 to November 2019, 166 patients were included (neoadjuvant 51, adjuvant 115). Compared with those who received adjuvant therapy, patients receiving NAT were younger (<35 years: 19.6% vs 5.2%, P=0.014), had larger tumors (T3: 62.7% vs 7.8%, P<0.001) and more advanced diseases (stage ⅡA: 2.0% vs 41.7%, P<0.001). Patients in the neoadjuvant group all received surgery, and 96 (83.5%) in the adjuvant group received anthracycline-and-taxane-containing regimens. A total of 98 patients (49 pairs) were matched, and the covariates between the two groups were acceptably balanced. Within a median follow-up of 46.5 (range, 14-87) months, the 4-year recurrence-free survival (RFS) rate among patients who received NAT was 73.3% (95% CI: 59.0%-87.6%), versus 80.6% (95% CI: 67.9%-93.3%) among those in the adjuvant group without statistical difference (P=0.418). A similar result was observed for the 4-year overall survival (OS) [neoadjuvant versus adjuvant: 91.5% (95% CI: 81.7%-100.0%) vs 97.8% (95% CI: 93.5%-100.0%), P=0.314]. Compared with standard adjuvant therapy, PCbH was related to less neutropenia and better cardiac safety. Conclusions: These results support the consideration of anthracycline-free neoadjuvant chemotherapy combined with anti-HER-2 therapy for patients with stages Ⅱ-Ⅲ HER-2-positive and HR-negative breast cancer. Optimized regimens with both efficacy and safety are needed and to be further investigated.

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[剂量密集紫杉醇加卡铂联合曲妥珠单抗新辅助治疗与标准辅助治疗对人表皮生长因子受体-2阳性和激素受体阴性乳腺癌:一项前瞻性队列研究]。
目的:为Ⅱ-Ⅲ期人表皮生长因子受体2 (HER-2)阳性和激素受体(HR)阴性乳腺癌患者提供无蒽环类新辅助化疗的生存证据。方法:前瞻性队列研究在中国医学科学院肿瘤医院肿瘤内科进行。HER-2阳性和HR阴性的Ⅱ-Ⅲ期乳腺癌患者,每两周接受高剂量紫杉醇(175 mg/m(2)) +卡铂(AUC=4.0)联合曲妥珠单抗(PCbH)的新辅助治疗(NAT),为期6个周期,并招募接受医生选择的标准辅助治疗的匹配患者进行生存和安全性比较。结果:2013年7月至2019年11月,纳入166例患者(新辅助51例,辅助115例)。与辅助治疗组相比,NAT组患者更年轻(P=0.014),肿瘤更大(T3: 62.7% vs 7.8%, PPCI: 59.0% ~ 87.6%),而辅助组患者的肿瘤更大(95% CI: 67.9% ~ 93.3%),差异无统计学意义(P=0.418)。在4年总生存率(OS)方面也观察到类似的结果[新辅助治疗vs辅助治疗:91.5% (95% CI: 81.7%-100.0%) vs 97.8% (95% CI: 93.5%-100.0%), P=0.314]。与标准辅助治疗相比,PCbH可减少中性粒细胞减少,提高心脏安全性。结论:这些结果支持对Ⅱ-Ⅲ期her -2阳性和hr -阴性乳腺癌患者考虑无蒽环类新辅助化疗联合抗her -2治疗。需要既有效又安全的优化方案,并有待进一步研究。
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
中华肿瘤杂志
中华肿瘤杂志 Medicine-Medicine (all)
CiteScore
1.40
自引率
0.00%
发文量
10433
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