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首页> 外文期刊>Breast cancer research and treatment. >Effects of trastuzumab on locoregional recurrence in human epidermal growth factor receptor 2-overexpressing breast cancer patients treated with chemotherapy and radiotherapy
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Effects of trastuzumab on locoregional recurrence in human epidermal growth factor receptor 2-overexpressing breast cancer patients treated with chemotherapy and radiotherapy

机译:曲妥珠单抗对化疗及放疗治疗人体表皮生长因子受体2-过度抑制乳腺癌患者的型患者的影响

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摘要

Purpose In the present study, the ability of adjuvant trastuzumab to reduce locoregional recurrence in patients with human epidermal growth factor receptor 2 (HER2)-overexpressing breast cancer receiving adjuvant chemotherapy and radiotherapy (RT) was investigated. Materials and methods We retrospectively included 520 patients with HER2-overexpressing breast cancer who received surgery followed by adjuvant RT and cytotoxic chemotherapy from 2003 to 2011. Adjuvant trastuzumab was administered to 286 patients. Propensity score matching was conducted to compare trastuzumab-treated and non-treated cohorts. Results Median follow-up duration was 7.1?years (range 1.1–14.1?years). Propensity score matching yielded 171 matched pairs of patients with no significantly different clinical factors. An improved 7-year locoregional control (LRC) rate was observed in the trastuzumab-treated cohort compared with the non-treated cohort (95.6% vs. 89.9%, p ?=?0.014). Based on multivariate analysis, hormone receptor negativity (hazard ratio [HR]?=?5.348, p ?=?0.007), positive lymph node ratio?>?0.25 (HR?=?2.549, p ?=?0.040), and lack of adjuvant trastuzumab (HR?=?3.401, p ?=?0.017) were identified as significant risk factors for poor LRC. Adjuvant trastuzumab significantly reduced the locoregional recurrence rate in patients with one or two risk factors (7-year LRC?=?95.0% vs. 84.2%, p ?=?0.007); however, the benefit of adjuvant trastuzumab was non-significant in patients with no risk factors (7-year LRC?=?95.8% vs. 97.9%, p ?=?0.75). Conclusions Adjuvant trastuzumab improved LRC in patients with HER2-overexpressing breast cancer receiving adjuvant RT and cytotoxic chemotherapy, especially in hormone receptor-negative, HER2-enriched subtype, and high positive lymph node ratio breast cancer.
机译:目的在本研究中,研究了佐剂曲妥珠单抗降低人表皮生长因子受体2(HER2)抑制乳腺癌接受佐剂化疗和放射治疗(RT)的患者患者患者患者的课程复发的能力。我们回顾性的材料和方法包括520例Her2过表达乳腺癌患者,他接受手术,然后从2003年到2011年接受佐剂Rt和细胞毒性化疗。佐剂曲妥珠酮施用至286名患者。进行倾向得分匹配以比较曲妥珠单抗治疗和未治疗的群体。结果中位后续时间为7.1?年(范围1.1-14.1?年)。倾向得分匹配产生171对患者没有明显不同的临床因素。与未处理的队列(95.6%与89.9%,P≥0.014)相比,在曲妥珠单抗治疗的队列中观察到曲妥珠豆采血治疗的队列中改善了7年的课程控制(LRC)速率。基于多变量分析,激素受体消极性(危险比[HR]?=?5.348,P?= 0.007),阳性淋巴结比?> 0.25(HR?=?2.549,P?= 0.040),缺乏佐剂曲妥珠单抗(HR?= 3.4.4.401,p?= 0.017)被鉴定为贫寒LRC的显着风险因素。佐剂曲妥珠单抗显着降低了一个或两个风险因素的患者的招生复发率(7年LRC?= 95.0%与84.2%,p?= 0.007);然而,佐剂曲妥珠单抗的益处在没有风险因素的患者中是非显着的(7年的LRC?=?95.8%与97.9%,p?= 0.75)。结论佐剂曲妥珠单抗改善了Her2-过度抑制乳腺癌患者的改良LRC,接受佐剂RT和细胞毒性化疗,特别是在激素受体阴性,海绵体,HER2富淋巴结率乳腺癌中。

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