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哌柏西利联合来曲唑作为一线治疗对雌激素受体阳性/人表皮生长因子受体2阴性晚期乳腺癌患者疼痛严重程度及疼痛对日常活动干扰的影响。

Impact of palbociclib plus letrozole on pain severity and pain interference with daily activities in patients with estrogen receptor-positive/human epidermal growth factor receptor 2-negative advanced breast cancer as first-line treatment.

作者信息

Bell T, Crown J P, Lang I, Bhattacharyya H, Zanotti G, Randolph S, Kim S, Huang X, Huang Bartlett C, Finn R S, Slamon D

机构信息

a Pfizer Inc. , New York , NY , USA ;

b St. Vincent's University Hospital , Dublin , Ireland ;

出版信息

Curr Med Res Opin. 2016 May;32(5):959-65. doi: 10.1185/03007995.2016.1157060. Epub 2016 Mar 2.

Abstract

Background Palbociclib is a recently approved drug for use in combination with letrozole as initial endocrine-based therapy for the treatment of postmenopausal women with advanced estrogen receptor-positive/human epidermal growth factor receptor 2-negative (ER+/HER2-) breast cancer. This report assesses the impact of palbociclib in combination with letrozole versus letrozole alone on patient-reported outcomes of pain. Methods Palbociclib was evaluated in an open-label, randomized, phase II study (PALOMA-1/TRIO-18) among postmenopausal women with advanced ER+/HER2- breast cancer who had not received prior systemic treatment for their advanced disease. Patients received continuous oral letrozole 2.5 mg daily alone or the same letrozole dose and schedule plus oral palbociclib 125 mg, given once daily for 3 weeks followed by 1 week off over repeated 28-day cycles. The primary study endpoint was investigator-assessed progression-free survival in the intent-to-treat population, and these results have recently been published (Finn et al., Lancet Oncol 2015;16:25-35). One of the key secondary endpoints was the evaluation of pain, as measured using the Brief Pain Inventory (BPI) patient-reported outcome tool. The BPI was administered at baseline and on day 1 of every cycle thereafter until disease progression and/or treatment discontinuation. Clinical trial registration This study is registered with ClinicalTrials.gov (NCT00721409). Results There were no statistically significant differences in Pain Severity or Pain Interference scores of the BPI between the two treatment groups for the overall population or among those with any bone disease at baseline. A limitation of the study is that results were not adjusted for the concomitant use of opioids or other medications used to control pain. Conclusions The addition of palbociclib to letrozole was associated with increased efficacy without negatively impacting pain severity or pain interference with daily activities.

摘要

背景

帕博西尼是一种最近获批的药物,可与来曲唑联合使用,作为绝经后晚期雌激素受体阳性/人表皮生长因子受体2阴性(ER+/HER2-)乳腺癌患者的初始内分泌治疗。本报告评估了帕博西尼联合来曲唑与单用 来曲唑相比,对患者报告的疼痛结局的影响。方法:在一项开放标签、随机、II期研究(PALOMA-1/TRIO-18)中,对未接受过晚期疾病全身治疗的绝经后晚期ER+/HER2-乳腺癌女性患者进行了帕博西尼评估。患者单独接受每日连续口服来曲唑2.5mg,或相同的来曲唑剂量和给药方案,加口服帕博西尼125mg,每日一次,服用3周,然后停药1周,重复28天周期。主要研究终点是意向性治疗人群中研究者评估的无进展生存期,这些结果最近已发表(Finn等人,《柳叶刀肿瘤学》2015年;16:25 - 35)。关键次要终点之一是使用简明疼痛量表(BPI)患者报告结局工具测量的疼痛评估。BPI在基线时以及此后每个周期的第1天进行评估,直至疾病进展和/或治疗中断。临床试验注册:本研究已在ClinicalTrials.gov(NCT00721409)注册。结果:在总体人群或基线时有任何骨病的人群中,两个治疗组之间BPI的疼痛严重程度或疼痛干扰评分没有统计学上的显著差异。该研究的一个局限性是,结果未针对阿片类药物或其他用于控制疼痛的药物的联合使用进行调整。结论:将帕博西尼添加到来曲唑中可提高疗效,而不会对疼痛严重程度或日常活动中的疼痛干扰产生负面影响。

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