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临床试验/NCT06003114
NCT06003114已完成不适用

Real-World Utilization of Palbociclib as 1L Treatment in Canadian HR+/HER2-women Breast Cancer Patients

Pfizer1 个研究点 分布在 1 个国家目标入组 472 人开始时间: 2023年10月6日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
Pfizer
入组人数
472
试验地点
1
主要终点
Estimate the median Duration of Treatment (DoT)

研究概览

简要总结

The purpose of this real-world study is to understand the use of palbociclib as first treatment for Hormone receptor positive (HR+) and Human epidermal growth factor receptor 2 negative (HER2-) metastatic breast cancer in Canada (PALCAN).

The real-world study is not a research study. It involves real patients who receive medicines prescribed by their doctors in the real world. Metastatic breast cancer is the type which has spread from breast to other organs.

HR positive stands for Hormone-receptor cells that have a protein on their surface that binds to one of 2 types of hormones. They are estrogen or progesterone. Both these hormones help cancer cells grow.

HER2 negative describes cells that have a small amount or none of a protein called HER2 on their surface. In normal cells, HER2 helps control cell growth. Cancer cells that are HER2 negative may grow more slowly and are less likely to come back or spread to other parts of the body.

This study will mainly measure:

- duration of treatment (from start of treatment till end of treatment) among a group of patients taking palbociclib (Ibrance) in combination with hormone therapy as first line treatment for HR+ HER2- metastatic breast cancer.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Received at least one cycle of palbociclib as first line therapy for metastatic breast cancer between 01 January 2016 and 31 December 2022
  • Histologically confirmed HR+/HER2- metastatic breast cancer
  • Minimum of 3 months available follow-up on palbociclib

排除标准

  • Received a different CDK4/6 inhibitor before palbociclib in the first line
  • Received other systemic therapy, including hormone therapy, 15-60 days prior to initiation of palbociclib
  • Invalid or incomplete records (more specifically, complete duration of treatment on palbociclib, endocrine therapy or LHRH)
  • Death date recorded on or before the date of index date

研究组 & 干预措施

First-line patients on Palbociclib

Participants taking oral palbociclib as prescribed in first-line treatment

干预措施: Palbociclib (Drug)

结局指标

主要结局

Estimate the median Duration of Treatment (DoT)

时间窗: Time index of approximately 01 Jan 2016 to 31 March 2022

次要结局

  • Number of patients with treatment discontinuation at one-year intervals(Time index of approximately 01 Jan 2016 to 31 March 2022)
  • Number of patients starting at initial dose(Time index of approximately 01 Jan 2016 to 31 March 2022)
  • Time to chemotherapy(Time index of approximately 01 Jan 2016 to 31 March 2022)
  • Clinical Characteristics of Patients(Time index of approximately 01 Jan 2016 to 31 March 2022)
  • Demographical Characteristics of Patients(Time index of approximately 01 Jan 2016 to 31 March 2022)

研究者

发起方
Pfizer
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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