Department of Medicine (Hematology/Oncology), University of California San Francisco, Helen Diller Family Comprehensive Cancer Center, 1600 Divisadero St, 2nd Floor, San Francisco, CA, 94115, USA.
Division of Hematology/Oncology, David Geffen School of Medicine at UCLA, Santa Monica, CA, USA.
Breast Cancer Res Treat. 2019 Apr;174(3):719-729. doi: 10.1007/s10549-018-05125-4. Epub 2019 Jan 10.
In the initial PALOMA-2 (NCT01740427) analysis with median follow-up of 23 months, palbociclib plus letrozole significantly prolonged progression-free survival (PFS) in women with estrogen receptor-positive (ER+)/human epidermal growth factor receptor 2-negative (HER2-) advanced breast cancer (ABC) [hazard ratio (HR) 0.58; P < 0.001]. Herein, we report results overall and by subgroups with extended follow-up.
In this double-blind, phase 3 study, post-menopausal women with ER+/HER2- ABC who had not received prior systemic therapy for their advanced disease were randomized 2:1 to palbociclib-letrozole or placebo-letrozole. Endpoints include investigator-assessed PFS (primary), safety, and patient-reported outcomes (PROs).
After a median follow-up of approximately 38 months, median PFS was 27.6 months for palbociclib-letrozole (n = 444) and 14.5 months for placebo-letrozole (n = 222) (HR 0.563; 1-sided P < 0.0001). All subgroups benefited from palbociclib treatment. The improvement of PFS with palbociclib-letrozole was maintained in the next 2 subsequent lines of therapy and delayed the use of chemotherapy (40.4 vs. 29.9 months for palbociclib-letrozole vs. placebo-letrozole). Safety data were consistent with the known profile. Patients' quality of life was maintained.
With approximately 15 months of additional follow-up, palbociclib plus letrozole continued to demonstrate improved PFS compared with placebo plus letrozole in the overall population and across all patient subgroups, while the safety profile remained favorable and quality of life was maintained. These data confirm that palbociclib-letrozole should be considered the standard of care for first-line therapy in patients with ER+/HER2- ABC, including those with low disease burden or long disease-free interval. Sponsored by Pfizer; ClinicalTrials.gov: NCT01740427.
在中位随访 23 个月的初始 PALOMA-2(NCT01740427)分析中,哌柏西利联合来曲唑显著延长了雌激素受体阳性(ER+)/人表皮生长因子受体 2 阴性(HER2-)晚期乳腺癌(ABC)患者的无进展生存期(PFS)[风险比(HR)0.58;P<0.001]。在此,我们报告了扩展随访后的总体结果和亚组结果。
在这项双盲、III 期研究中,未接受过晚期疾病系统治疗的绝经后 ER+/HER2-ABC 女性患者按 2:1 随机分配至哌柏西利-来曲唑或安慰剂-来曲唑组。主要终点为研究者评估的 PFS(首要终点)、安全性和患者报告的结局(PROs)。
中位随访约 38 个月后,哌柏西利-来曲唑组(n=444)和安慰剂-来曲唑组(n=222)的中位 PFS 分别为 27.6 个月和 14.5 个月(HR 0.563;单侧 P<0.0001)。所有亚组均从哌柏西利治疗中获益。哌柏西利-来曲唑治疗的 PFS 改善在随后的 2 线治疗中得以维持,并延迟了化疗的使用(哌柏西利-来曲唑组 vs. 安慰剂-来曲唑组分别为 40.4 个月和 29.9 个月)。安全性数据与已知特征一致。患者的生活质量得到维持。
在大约 15 个月的额外随访中,哌柏西利联合来曲唑与安慰剂联合来曲唑相比,在总体人群和所有患者亚组中均继续显示出改善的 PFS,同时安全性特征保持有利,生活质量得以维持。这些数据证实,哌柏西利-来曲唑应被视为 ER+/HER2-ABC 患者一线治疗的标准治疗方案,包括疾病负担低或无疾病间期长的患者。由辉瑞公司赞助;ClinicalTrials.gov:NCT01740427。