Deparmtent of Medicine, Roswell Park Comprehensive Cancer Center, Buffalo, NY.
Department of Pharmacy, Roswell Park Comprehensive Cancer Center, Buffalo, NY.
Clin Breast Cancer. 2018 Dec;18(6):e1401-e1405. doi: 10.1016/j.clbc.2018.04.015. Epub 2018 Apr 28.
Outcome data on hormone receptor positive (HR), human epidermal growth factor receptor 2 (HER2) nonamplified (HER2) metastatic breast cancer (MBC) treated with palbociclib after treatment with everolimus are lacking. The PALOMA-3 trial, showing benefit of palbociclib plus fulvestrant compared to fulvestrant alone in HRHER2 MBC after progression while receiving endocrine therapy excluded women previously treated with everolimus. The objective of this study was to examine outcomes of HRHER2 MBC with prior exposure to everolimus while receiving palbociclib-based therapy.
A retrospective, single-institute review was conducted of HRHER2 MBC from January 2014 to November 2016 in patients treated with palbociclib after prior treatment with everolimus. Progression-free survival (PFS) was defined as the time from initiation of palbociclib to the date of progression as determined by the treating physician based on radiologic, biochemical, and/or clinical criteria. Response rates were determined on the basis of available radiologic data. Objective response rate (ORR) was defined as the rate of any complete or partial responses; clinical benefit rate (CBR) was the rate of complete response, partial response, or stable disease for at least 24 weeks.
Twenty-three patients with a mean (range) age of 68 (42-81) years were identified. Kaplan-Meier estimate showed median PFS of 2.9 months (95% confidence interval, 2.1-4.2); ORR was 0 of 23 and CBR was 4 (17.4%) of 23. In the PALOMA-3 trial, median PFS, ORR, and CBR of palbociclib cohort were 9.5 months (95% confidence interval, 9.2-11.0), 19%, and 67%, respectively.
There is a limited clinical activity of palbociclib combinations after progression with everolimus combination therapy. Further studies are necessary to confirm these findings.
在接受依维莫司治疗后,对于激素受体阳性(HR)、人表皮生长因子受体 2(HER2)无扩增(HER2)转移性乳腺癌(MBC)患者,使用帕博西尼治疗的结局数据缺乏。PALOMA-3 试验显示,与单独使用氟维司群相比,在接受内分泌治疗进展后,HRHER2MBC 患者使用帕博西尼联合氟维司群治疗具有获益,该试验排除了先前接受过依维莫司治疗的女性。本研究的目的是检查先前接受过依维莫司治疗,且正在接受帕博西尼为基础的治疗的 HRHER2MBC 患者的结局。
对 2014 年 1 月至 2016 年 11 月期间,在先前接受依维莫司治疗后使用帕博西尼治疗的 HRHER2MBC 患者进行了回顾性、单中心研究。无进展生存期(PFS)定义为从帕博西尼起始时间至根据影像学、生化和/或临床标准确定的进展日期的时间。根据可获得的影像学数据确定缓解率。客观缓解率(ORR)定义为任何完全或部分缓解的发生率;临床获益率(CBR)为完全缓解、部分缓解或疾病稳定至少 24 周的发生率。
确定了 23 例患者,平均(范围)年龄为 68 岁(42-81 岁)。Kaplan-Meier 估计显示中位 PFS 为 2.9 个月(95%置信区间,2.1-4.2);23 例患者中 ORR 为 0,CBR 为 4(17.4%)。在 PALOMA-3 试验中,帕博西尼组的中位 PFS、ORR 和 CBR 分别为 9.5 个月(95%置信区间,9.2-11.0)、19%和 67%。
在依维莫司联合治疗进展后,帕博西尼联合治疗的临床疗效有限。需要进一步的研究来证实这些发现。