Olga Oikonomidou, Mark J Beresford, Elena Galve-Calvo, Achim Woeckel, Rohan C Parikh, Abigail Hitchens, Connie Chen, Justin Doan, Benjamin Li, Valerie Derrien Ansquer, Gaelle Frugier, Maria I Jimenez, Keith L Davis, Edward I Broughton
{"title":"在欧洲,HR+/HER2-晚期乳腺癌患者一线帕博西尼和芳香酶抑制剂治疗相关的真实世界临床结果","authors":"Olga Oikonomidou, Mark J Beresford, Elena Galve-Calvo, Achim Woeckel, Rohan C Parikh, Abigail Hitchens, Connie Chen, Justin Doan, Benjamin Li, Valerie Derrien Ansquer, Gaelle Frugier, Maria I Jimenez, Keith L Davis, Edward I Broughton","doi":"10.1007/s10549-025-07707-5","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>Cyclin-dependent kinase 4/6 inhibitors (CDK4/6is) combined with endocrine therapy is the recommended first-line (1L) treatment for hormone receptor-positive and human epidermal growth factor receptor 2-negative (HR+/HER2-) advanced breast cancer (ABC). Real-world evidence (RWE) describing 1L CDK4/6i regimens and associated clinical outcomes in Europe is limited. The study objective was to describe clinical characteristics, tumor response, and survival outcomes in patients with HR+/HER2- ABC.</p><p><strong>Methods: </strong>This retrospective, observational cohort study used data from 52 treatment centers in the UK, Spain, and Germany and included patients who initiated 1L palbociclib + aromatase inhibitor (AI) therapy for ABC between 2016 and 2020. Primary endpoints were real-world progression-free survival (rwPFS) and overall survival (OS).</p><p><strong>Results: </strong>Data were abstracted from 856 patients. During treatment, complete response, partial response, or stable disease was achieved for 86.1% of patients in Spain, 80.7% in the UK, and 79.0% in Germany, while complete or partial response was achieved for 43.8% of patients in Spain, 34.9% in the UK, and 16.9% in Germany. Median rwPFS during treatment was 28.1 months for patients in Spain, 33.9 months in the UK, and 48.1 months in Germany. Median OS was 51.3 months (95% CI 46.6-NE) in the UK, 65.2 months (95% CI 65.2-NE) in Germany, and not reached in Spain.</p><p><strong>Conclusion: </strong>This RWE supports the clinical effectiveness of 1L palbociclib + AI in routine clinical practice in European countries-consistent with the efficacy observed in clinical trials-and further supports the implementation of palbociclib-based regimens as frontline treatment of HR+/HER2- ABC.</p>","PeriodicalId":9133,"journal":{"name":"Breast Cancer Research and Treatment","volume":" ","pages":"299-312"},"PeriodicalIF":3.0000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12396976/pdf/","citationCount":"0","resultStr":"{\"title\":\"Real-world clinical outcomes associated with first-line palbociclib and aromatase inhibitor therapy among patients with HR+/HER2- advanced breast cancer in Europe.\",\"authors\":\"Olga Oikonomidou, Mark J Beresford, Elena Galve-Calvo, Achim Woeckel, Rohan C Parikh, Abigail Hitchens, Connie Chen, Justin Doan, Benjamin Li, Valerie Derrien Ansquer, Gaelle Frugier, Maria I Jimenez, Keith L Davis, Edward I Broughton\",\"doi\":\"10.1007/s10549-025-07707-5\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Purpose: </strong>Cyclin-dependent kinase 4/6 inhibitors (CDK4/6is) combined with endocrine therapy is the recommended first-line (1L) treatment for hormone receptor-positive and human epidermal growth factor receptor 2-negative (HR+/HER2-) advanced breast cancer (ABC). Real-world evidence (RWE) describing 1L CDK4/6i regimens and associated clinical outcomes in Europe is limited. The study objective was to describe clinical characteristics, tumor response, and survival outcomes in patients with HR+/HER2- ABC.</p><p><strong>Methods: </strong>This retrospective, observational cohort study used data from 52 treatment centers in the UK, Spain, and Germany and included patients who initiated 1L palbociclib + aromatase inhibitor (AI) therapy for ABC between 2016 and 2020. Primary endpoints were real-world progression-free survival (rwPFS) and overall survival (OS).</p><p><strong>Results: </strong>Data were abstracted from 856 patients. During treatment, complete response, partial response, or stable disease was achieved for 86.1% of patients in Spain, 80.7% in the UK, and 79.0% in Germany, while complete or partial response was achieved for 43.8% of patients in Spain, 34.9% in the UK, and 16.9% in Germany. Median rwPFS during treatment was 28.1 months for patients in Spain, 33.9 months in the UK, and 48.1 months in Germany. Median OS was 51.3 months (95% CI 46.6-NE) in the UK, 65.2 months (95% CI 65.2-NE) in Germany, and not reached in Spain.</p><p><strong>Conclusion: </strong>This RWE supports the clinical effectiveness of 1L palbociclib + AI in routine clinical practice in European countries-consistent with the efficacy observed in clinical trials-and further supports the implementation of palbociclib-based regimens as frontline treatment of HR+/HER2- ABC.</p>\",\"PeriodicalId\":9133,\"journal\":{\"name\":\"Breast Cancer Research and Treatment\",\"volume\":\" \",\"pages\":\"299-312\"},\"PeriodicalIF\":3.0000,\"publicationDate\":\"2025-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12396976/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Breast Cancer Research and Treatment\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1007/s10549-025-07707-5\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/8/6 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Breast Cancer Research and Treatment","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s10549-025-07707-5","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/8/6 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
目的:细胞周期蛋白依赖性激酶4/6抑制剂(CDK4/6is)联合内分泌治疗是激素受体阳性和人表皮生长因子受体2阴性(HR+/HER2-)晚期乳腺癌(ABC)推荐的一线(1L)治疗方法。在欧洲,描述1L CDK4/6i方案和相关临床结果的真实证据(RWE)是有限的。研究目的是描述HR+/HER2- ABC患者的临床特征、肿瘤反应和生存结局。方法:这项回顾性、观察性队列研究使用了来自英国、西班牙和德国的52个治疗中心的数据,包括2016年至2020年间接受1L帕博西尼+芳香酶抑制剂(AI)治疗ABC的患者。主要终点为真实世界无进展生存期(rwPFS)和总生存期(OS)。结果:从856例患者中提取数据。在治疗期间,西班牙86.1%、英国80.7%和德国79.0%的患者达到完全缓解、部分缓解或疾病稳定,而西班牙43.8%、英国34.9%和德国16.9%的患者达到完全缓解或部分缓解。西班牙患者治疗期间的中位rwPFS为28.1个月,英国为33.9个月,德国为48.1个月。中位OS在英国为51.3个月(95% CI 46.6-NE),在德国为65.2个月(95% CI 65.2- ne),在西班牙没有达到。结论:该RWE支持1L palbociclib + AI在欧洲国家常规临床实践中的临床有效性,与临床试验观察到的疗效一致,并进一步支持以palbociclib为基础的方案作为HR+/HER2- ABC的一线治疗方案的实施。
Real-world clinical outcomes associated with first-line palbociclib and aromatase inhibitor therapy among patients with HR+/HER2- advanced breast cancer in Europe.
Purpose: Cyclin-dependent kinase 4/6 inhibitors (CDK4/6is) combined with endocrine therapy is the recommended first-line (1L) treatment for hormone receptor-positive and human epidermal growth factor receptor 2-negative (HR+/HER2-) advanced breast cancer (ABC). Real-world evidence (RWE) describing 1L CDK4/6i regimens and associated clinical outcomes in Europe is limited. The study objective was to describe clinical characteristics, tumor response, and survival outcomes in patients with HR+/HER2- ABC.
Methods: This retrospective, observational cohort study used data from 52 treatment centers in the UK, Spain, and Germany and included patients who initiated 1L palbociclib + aromatase inhibitor (AI) therapy for ABC between 2016 and 2020. Primary endpoints were real-world progression-free survival (rwPFS) and overall survival (OS).
Results: Data were abstracted from 856 patients. During treatment, complete response, partial response, or stable disease was achieved for 86.1% of patients in Spain, 80.7% in the UK, and 79.0% in Germany, while complete or partial response was achieved for 43.8% of patients in Spain, 34.9% in the UK, and 16.9% in Germany. Median rwPFS during treatment was 28.1 months for patients in Spain, 33.9 months in the UK, and 48.1 months in Germany. Median OS was 51.3 months (95% CI 46.6-NE) in the UK, 65.2 months (95% CI 65.2-NE) in Germany, and not reached in Spain.
Conclusion: This RWE supports the clinical effectiveness of 1L palbociclib + AI in routine clinical practice in European countries-consistent with the efficacy observed in clinical trials-and further supports the implementation of palbociclib-based regimens as frontline treatment of HR+/HER2- ABC.
期刊介绍:
Breast Cancer Research and Treatment provides the surgeon, radiotherapist, medical oncologist, endocrinologist, epidemiologist, immunologist or cell biologist investigating problems in breast cancer a single forum for communication. The journal creates a "market place" for breast cancer topics which cuts across all the usual lines of disciplines, providing a site for presenting pertinent investigations, and for discussing critical questions relevant to the entire field. It seeks to develop a new focus and new perspectives for all those concerned with breast cancer.