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帕博西尼联合治疗的真实世界治疗模式和临床结局:来自艾伯维真实世界洞察研究的一项多国汇总分析。

Real-world Treatment Patterns and Clinical Outcomes Associated With Palbociclib Combination Therapy: A Multinational, Pooled Analysis From the Ibrance Real World Insights Study.

机构信息

Adelphi Real World, Bollington, United Kingdom.

Pfizer, New York, New York.

出版信息

Clin Ther. 2022 Dec;44(12):1588-1601. doi: 10.1016/j.clinthera.2022.11.004. Epub 2022 Nov 28.

Abstract

PURPOSE

Palbociclib was the first cyclin-dependent kinase 4/6 inhibitor approved by the US Food and Drug Administration for use in combination with aromatase inhibitors (AIs) as initial endocrine-based therapy or with fulvestrant in postmenopausal women who previously received endocrine therapy based on data from randomized clinical trials. Real-world studies examining the effectiveness of palbociclib in large, diverse patient populations in routine clinical practice were needed.

PATIENTS AND METHODS

Ibrance Real World Insights (IRIS) was a retrospective medical record review study of women with confirmed hormone receptor-positive, HER2-negative advanced/metastatic breast cancer treated with palbociclib plus an AI or with palbociclib plus fulvestrant according to approved indications. Participating physicians reviewed medical records of up to 16 sequentially presenting patients, collecting demographic and clinical data. Outcomes included objective response rates, progression-free rates, and survival rates overall and in patients stratified according to age, race and ethnicity, Eastern Cooperative Oncology Group (ECOG) performance status (PS), disease-free interval, visceral disease, liver metastases, bone-only metastases, and previous lines of therapy.

FINDINGS

Data were abstracted by 417 physicians for 2954 patients in 13 countries; 1415 patients (47.9%) were ≥65 years of age, 369 patients (12.5%) had an ECOG PS ≥2 at initiation, and 835 patients (28.3%) were races other than White. The 12-month progression-free rate was 88% for palbociclib plus an AI and 79% for palbociclib plus fulvestrant; the 12-month survival rate was 96% in both groups. The objective response rates were 80% for palbociclib plus an AI and 75% for palbociclib plus fulvestrant. Palbociclib was similarly effective in most subgroups examined.

IMPLICATIONS

Data from IRIS provide in-depth, real-world evidence for the use of palbociclib in a range of breast cancer populations in multiple countries. These data support the findings of the randomized PALOMA-2 and PALOMA-3 studies.

摘要

目的

帕博西尼是首个获美国食品药品监督管理局批准的细胞周期蛋白依赖性激酶 4/6 抑制剂,可与芳香化酶抑制剂(AI)联合用于初始内分泌治疗,或与氟维司群联合用于接受基于内分泌的既往治疗后进展的绝经后妇女,其数据来自随机临床试验。需要来自真实世界研究的数据来评估帕博西尼在常规临床实践中广泛多样的患者人群中的疗效。

患者和方法

Ibrance 真实世界洞察(IRIS)是一项回顾性病历审查研究,纳入了根据批准适应证接受帕博西尼联合 AI 或帕博西尼联合氟维司群治疗的确诊为激素受体阳性、HER2 阴性的晚期/转移性乳腺癌女性患者。参与研究的医生对最多 16 例连续就诊患者的病历进行回顾,收集人口统计学和临床数据。主要终点包括总人群及根据年龄、种族和民族、东部肿瘤协作组(ECOG)体能状态(PS)、无病间期、内脏疾病、肝转移、单纯骨转移和既往治疗线数进行分层的客观缓解率、无进展率和生存率。

结果

共 417 名医生在 13 个国家对 2954 例患者的数据进行了提取;1415 例(47.9%)患者≥65 岁,369 例(12.5%)患者起始时 ECOG PS ≥2,835 例(28.3%)患者为非白种人。帕博西尼联合 AI 组的 12 个月无进展率为 88%,帕博西尼联合氟维司群组为 79%;两组的 12 个月生存率均为 96%。帕博西尼联合 AI 组的客观缓解率为 80%,帕博西尼联合氟维司群组为 75%。在大多数亚组中,帕博西尼的疗效相当。

结论

IRIS 数据提供了来自多个国家的广泛乳腺癌人群中使用帕博西尼的深入、真实世界的证据。这些数据支持 PALOMA-2 和 PALOMA-3 随机研究的结果。

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