A multicenter analysis of treatment patterns and clinical outcomes of subsequent therapies after progression on palbociclib in HR+/HER2− metastatic breast cancer

帕博西利布 医学 内科学 肿瘤科 依西美坦 转移性乳腺癌 卡培他滨 紫杉烷 化疗 长春瑞滨 乳腺癌 无进展生存期 拉帕蒂尼 癌症 妇科 曲妥珠单抗 三苯氧胺 顺铂 结直肠癌
作者
Yi Li,Wei Li,Chengcheng Gong,Yabin Zheng,Quchang Ouyang,Ning Xie,Qing Qu,Rui Ge,Biyun Wang
出处
期刊:Therapeutic Advances in Medical Oncology [SAGE Publishing]
卷期号:13: 17588359211022890-17588359211022890 被引量:41
标识
DOI:10.1177/17588359211022890
摘要

Introduction: Endocrine therapy and cyclin-dependent kinase (CDK) 4/6 inhibitors (CDK4/6i) are standard treatment options for hormone receptor positive (HR+)/human epidermal growth factor receptor 2 negative (HER2–) metastatic breast cancer (MBC). However, the efficacy of standard subsequent therapies after CDK4/6i-based treatment is unclear. This study aimed to examine physician practice patterns and treatment outcomes of subsequent therapies administered after progression on palbociclib therapy in clinical practice. Methods: The study included 200 patients with HR+/HER2– MBC who underwent subsequent treatments after progressing on palbociclib-based regimens in five Chinese institutions between August 2017 and April 2020. The treatment pattern, progression-free survival (PFS), overall survival (OS), and objective response rate (ORR) were reported. Results: A total of 200 patients were included, of whom 147 (73.5%) and 53 (26.5%) received subsequent chemotherapy and endocrine therapy, respectively. The frequently used monochemotherapy regimens were taxane ( n = 29), capecitabine ( n = 21), and vinorelbine ( n = 17), while the endocrine therapy regimens were chidamide plus exemestane ( n = 16) and everolimus plus exemestane ( n = 9). The overall median PFS (mPFS) was 5.5 months, with no significant difference in mPFS between the chemotherapy and endocrine therapy groups ( p = 0.669). However, among patients not sensitive to prior palbociclib treatment, those administered chemotherapy had significantly longer PFS than those administered endocrine therapy ( p = 0.006). The mPFS with endocrine therapy after first-, second-, and subsequent-line palbociclib was 13.4, 3.1, and 4.1 months, respectively ( p = 0.233); in contrast, the mPFS with chemotherapy was 7.2, 6.5, and 4.9 months after first-, second-, and subsequent-line palbociclib, respectively ( p = 0.364). The median OS was not achieved. The ORR was 10.6% among the 198 patients included in the analysis. Conclusions: Physicians prefer chemotherapy over endocrine therapy for the treatment of patients with HR+/HER2– MBC who develop progression on palbociclib. Sensitivity to previous palbociclib treatment might be one of the indicators for predicting response to subsequent treatment. ClinicalTrials.gov identifier: NCT04517318
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
几米完成签到,获得积分10
刚刚
1秒前
Owen应助初识采纳,获得10
1秒前
3秒前
xss完成签到 ,获得积分10
5秒前
几米发布了新的文献求助10
5秒前
拼搏以亦发布了新的文献求助10
6秒前
苹果曼香发布了新的文献求助10
7秒前
激昂的访曼完成签到,获得积分10
9秒前
9秒前
Hello应助LLGGZZYY采纳,获得10
12秒前
碧蓝破茧发布了新的文献求助10
12秒前
拾捌发布了新的文献求助10
13秒前
16秒前
17秒前
18秒前
他化自在天完成签到,获得积分10
19秒前
博慧完成签到 ,获得积分10
20秒前
生动又夏完成签到,获得积分10
20秒前
22秒前
小六六呢发布了新的文献求助10
22秒前
WCC发布了新的文献求助20
22秒前
23秒前
ralm完成签到,获得积分10
24秒前
科目三应助weixiao采纳,获得10
26秒前
Jasper应助儒雅的月光采纳,获得10
28秒前
28秒前
wth发布了新的文献求助10
28秒前
31秒前
布布完成签到,获得积分10
31秒前
32秒前
32秒前
32秒前
32秒前
称心巧荷发布了新的文献求助10
34秒前
Alicia完成签到,获得积分10
34秒前
河不柃发布了新的文献求助10
35秒前
小小鱼发布了新的文献求助10
36秒前
orixero应助称心的新之采纳,获得10
36秒前
小解发布了新的文献求助10
36秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Atlas of Aligner Treatment and Planning A Case-Based Approach 1000
Geist der Kunst und Kultur 1000
悉尼大学博士学位论文,题目:Modelling and testing of one-sided stitched laminated composites. 作者:Kristopher P. Plain 700
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
丝光沸石活性位点定向调控及其二甲醚羰基化性能研究 500
A Concise History of the World, 2nd Edition 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7422395
求助须知:如何正确求助?哪些是违规求助? 9025452
关于积分的说明 19227198
捐赠科研通 7052246
什么是DOI,文献DOI怎么找? 3235261
关于科研通互助平台的介绍 2398272
邀请新用户注册赠送积分活动 2217664