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Health-related quality of life in patients receiving first-line eribulin mesylate with or without trastuzumab for locally recurrent or metastatic breast cancer

机译:与局部复发或转移性乳腺癌接受一线二林蛋白甲磺酸盐的患者与局部复发或转移性乳腺癌的患者的健康有关的生活质量

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Eribulin mesylate is a nontaxane microtubule dynamics inhibitor approved for second-line (European Union) or third-line (United States) treatment of metastatic breast cancer. Two phase 2 single trials, evaluating first-line eribulin as monotherapy (Study 206; NCT01268150) or in combination with trastuzumab (Study 208; NCT01269346) in locally recurrent or metastatic breast cancer, demonstrated objective response rates of 28.6 and 71.2%, respectively. Median progression-free survival was 6.8 and 11.6?months, respectively. Tolerability profiles were similar to those from previous studies. This secondary analysis was conducted to assess health-related quality of life (HRQoL) in both phase 2 trials. Patients received eribulin mesylate 1.4?mg/m2 intravenously on days 1 and 8 of each 21-day?cycle. Patients in Study 208 also received intravenous trastuzumab on day 1 of each cycle (8?mg/kg in cycle 1, then 6?mg/kg). HRQoL was assessed by the European Organization for Research and Treatment of Cancer Quality-of-Life (QLQ-C30) assessment tool and the Quality-of-Life Questionnaire for Breast Cancer (QLQ-BR23) at baseline and cycles 2, 4, and 6. Results for clinically meaningful changes were based on previously published minimum important differences. Of the 108 patients (56 in Study 206 and 52 in Study 208) treated, 57 and 87%, respectively, completed 6?cycles. Completion rates for both questionnaires were 94 and 98%, respectively, at cycle 6. Most patients had stable/improved HRQoL scores with some exceptions; for example, more patients experienced a worsening in cognitive functioning and systemic therapy side effects than experienced improvement. Mean QLQ-C30 symptom scores correlated with corresponding adverse event rates for nausea/vomiting, dyspnea, appetite loss, constipation, and diarrhea in Study 206 and for fatigue, nausea/vomiting, pain, dyspnea, insomnia, constipation, and diarrhea in Study 208. First-line eribulin ± trastuzumab therapy did not lead to deterioration of overall HRQoL in most patients, with more than 60% of patients having stable/improved global health status/quality-of-life scores. Eribulin has been demonstrated to be comparable with other chemotherapy agents with an acceptable safety profile. Therefore, further evaluation is warranted to determine whether eribulin ± trastuzumab therapy may be a potential option for first-line treatment in some patients with metastatic breast cancer who were recently treated in the neoadjuvant setting. NCT01268150 (December 29, 2010), NCT01269346 (January 4, 2011).
机译:Eribulin甲磺酸盐是批准用于二线(欧盟)或第三线(美国)治疗转移性乳腺癌的尿烷微管动态抑制剂。两相2单试验,评估一线二林蛋白作为单一疗法(研究206; NCT01268150)或与局部复发性或转移性乳腺癌的曲妥珠单抗(研究208; NCT01269346组合,分别表现出28.6和71.2%的目标响应率。中位进展生存率分别为6.8和11.6?几个月。可耐受性曲线与来自之前的研究的概况类似。进行该二级分析以评估两项试验中的健康相关的生命质量(HRQOL)。患者在每21天的第1天和第8天静脉内接受Eribulin甲磺酸盐1.4?mg / m 2。研究中的患者208还在每个循环的第1天(循环1中的8毫克/千克,然后6μmg/ kg)接受静脉内曲妥珠单抗。 HRQOL是由欧洲癌症质量(QLQ-C30)评估工具的研究和治疗组织和乳腺癌(QLQ-BR23)的母乳癌(QLQ-BR23)的研究和治疗组织进行评估。基线和循环2,4和6.临床有意义的变化的结果是基于以前公布的最小重要差异。在108名患者(研究206和52中的56例208)中,治疗,57和87%,完成6?循环。循环6分别为94和98%的问卷的完成率分别为94%,大多数患者稳定/改善了HRQOL分数,具有一些例外;例如,更多患者在认知功能和系统性治疗副作用中经历了恶化而不是经历的改进。平均QLQ-C30症状分数与对应的恶心/呕吐,呼吸困难,食欲,食欲损失,便秘和腹泻的相应不良事件率相关,疲劳,恶心/呕吐,疼痛,呼吸困难,呼吸困难,呼吸困难208中的研究208 。第一线Eribulin±Trastuzumab疗法在大多数患者中没有导致整体HRQOL的恶化,超过60%的患者稳定/改善全球卫生地位/生活质量分数。已经证明Eribulin与其他化疗剂相当,具有可接受的安全性。因此,有必要进一步评估以确定Eribulin±Trastuzumab治疗是否可能是在新辅助环境中最近治疗的一些转移性乳腺癌患者中的一线治疗的潜在选择。 NCT01268150(2010年12月29日),NCT01269346(2011年1月4日)。

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