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帕博西尼用于晚期激素受体阳性乳腺癌:来自智利多中心注册研究的真实世界数据。

Palbociclib in advanced stage hormone receptor-positive breast cancer: real-world data from a Chilean multicentre registry.

作者信息

Walbaum Benjamín, Reyes José Miguel, Rodriguez Pablo, Muñiz Sabrina, Medina Lidia, Ibañez Carolina, Merino Tomas, Pinto Mauricio P, Bravo Maria Loreto, Acevedo Francisco, Bennett José, Sanchez Cesar

机构信息

Department of Hematology-Oncology, Faculty of Medicine, Pontificia Universidad Católica de Chile, Santiago 8330077, Chile.

Dr. Sótero del Río Hospital and Healthcare Complex, Santiago 8207257, Chile.

出版信息

Ecancermedicalscience. 2023 Nov 21;17:1636. doi: 10.3332/ecancer.2023.1636. eCollection 2023.

DOI:10.3332/ecancer.2023.1636
PMID:38414945
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10898906/
Abstract

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 ( = 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.

摘要

背景

在内分泌治疗(ET)基础上加用细胞周期蛋白依赖性激酶抑制剂(CDKi)作为一线或二线治疗,可改善激素受体阳性、人表皮生长因子受体2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哌柏西利作为一线或后续(≥二线)治疗的智利患者的生存率和预后因素。

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年总生存期,并进行多变量分析以确定预后因素。

结果

共纳入106例患者。中位年龄为49岁(19 - 86岁),28.3%(30例)为初发IV期疾病;63%的患者接受哌柏西利联合ET作为一线治疗,其中54%使用芳香化酶抑制剂而非氟维司群。整个队列的中位总生存期为99个月,5年总生存率为69%。接受一线哌柏西利治疗的患者5年总生存率为89%,而ET单药治疗或≥二线哌柏西利治疗的患者为43%(P = 0.0062)。多变量分析显示,诊断年份和CDKi使用时机(一线治疗与≥二线治疗)与总生存期显著相关。

结论

我们的真实世界数据表明,在HR+/HER2- ABC患者中,一线CDKi + ET与≥二线治疗相比,在总生存期方面具有统计学上的显著优势。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43ae/10898906/a0243ffaed48/can-17-1636fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43ae/10898906/a0243ffaed48/can-17-1636fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43ae/10898906/a0243ffaed48/can-17-1636fig1.jpg

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