Benjamín Walbaum, José Miguel Reyes, Pablo Rodriguez, S. Muniz, L. Medina, C. Ibañez, T. Merino, Mauricio P Pinto, M. Bravo, Francisco Acevedo, José Bennett, C. Sánchez
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引用次数: 0
摘要
背景:在内分泌治疗(ET)的一线或二线治疗中加入细胞周期蛋白依赖性激酶抑制剂(CDKi)可改善激素受体阳性、HER2阴性(HR+/HER2-)晚期乳腺癌(ABC)患者的无进展生存期和总生存期(OS)。我们的研究比较了在真实世界中使用帕博西尼(palbociclib)作为一线或后续(≥二线)治疗的智利患者的生存率和预后因素。研究方法我们的回顾性人群队列研究纳入了HR+/HER2-ABC患者。我们计算了5年OS,并进行了多变量分析以确定预后因素。研究结果共纳入 106 例患者。中位年龄为49岁(19-86岁),28.3%(30人)患有新发IV期疾病;63%的患者接受了帕博西尼联合ET作为一线治疗,其中54%的患者使用芳香化酶抑制剂而非氟维司群。整个组群的中位OS为99个月,5年OS为69%。接受帕博西尼一线治疗的患者的5年生存率为89%,而接受ET单药治疗或≥二线帕博西尼治疗的患者的5年生存率为43% ( p = 0.0062)。多变量分析显示,诊断年份和 CDKi 时间(一线与≥二线)与 OS 显著相关。结论我们的实际数据显示,在HR+/HER2-ABC患者中,一线CDKi+ET与≥二线CDKi+ET相比,在OS方面具有统计学意义上的显著优势。
Palbociclib in advanced stage hormone receptor-positive breast cancer: real- world data from a Chilean multicentre registry
Background: The addition of cyclin-dependent kinases inhibitors (CDKi) to endocrine therapy (ET) as the first-or second line treatment improves progression-free and overall survival (OS) in hormone receptor-positive, HER2 negative (HR+/HER2-) advanced stage breast cancer (ABC). Our study compared survival rates and prognostic factors in Chilean patients that used palbociclib as first or subsequent (≥second) lines of treatment in a real-world setting. Methods: Our retrospective population-cohort study included HR+/HER2-ABC patients. We calculated 5-year OS and performed a multivariate analysis to determine prognostic factors. Results: A total of 106 patients were included. Median age was 49 years (19–86), 28.3% (30) had de novo stage IV disease; 63% received palbociclib with ET as first line, 54% of them with aromatase inhibitor over fulvestrant. Median OS for the entire cohort was 99 months and 5-year OS was 69%. Patients that received first line palbociclib had a 5-year OS of 89% versus 43% for ET monotherapy or ≥second line palbociclib ( p = 0.0062). Multivariate analysis showed that the year at diagnosis and CDKi timing (first line versus ≥second line) were significantly associated with OS. Conclusion: Our real-world data show that first-line CDKi + ET provides a statistically significant benefit in OS versus ≥second line in HR+/HER2-ABC patients.