跳至主要内容
临床试验/NCT03245112
NCT03245112Unknown不适用

Retrospective Data Collection and Analysis of the Therapeutic Effect of Eribulin for Advanced Breast Cancer Patients.

Chang Gung Memorial Hospital1 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2014年3月3日最近更新:
适应症
相关药物

试验速览

阶段
不适用
发起方
入组人数
500
试验地点
1
主要终点
Disease Control Rate (DCR)

研究概览

简要总结

Since the first marketing authorization in the world in November 2010 granted by US FDA, Halaven has been approved for clinical use in more than 40 countries worldwide, including many Asian countries, e.g. Hong Kong, India, Japan, Malaysia, Myanmar, Philippines, South Korea, Singapore, Taiwan and Thailand. According to two large global phase III study reports of Halaven, very few Asian patients participated in these studies. In a phase II study of Halaven with metastatic breast cancer, the clinical efficacy and toxicity were reported only in 80 Japanese patients. Halaven has been granted its marketing authorization in Singapore since February 2011. However, most of other Asian countries including India have had the approval and launched from middle year of 2013 or in early 2014. Limited information of Halaven using in Asian patients are available except several case experience exchange presented by individual medical centers or as personal experience in the past. Some clinical concerns related to Halaven use are raised by clinicians during their clinical practice, such as how Halaven works on Asian patients, which type of patient obtains better clinical benefit from Halaven, and what are the main treatment related toxicities in Asian which may differ from Westerners due to potential ethnic diversity. Further understanding of Halaven related clinical benefit and toxicity in Asian patients through collecting clinical experience among Asian countries becomes necessary and may provide better information to anticipate these concerns.

The proposed "Halaven Patient Registry" (called the "Registry") will be a patient population-based registry to collect therapeutic related information from patients with metastatic breast cancer who were treated with Halaven that was given as a clinical decision by patient's treating physician based on clinical status of a patient and proper indication of Halaven and to gain a better understanding of the use of Halaven in such Asian patients.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Other

入排标准

年龄范围
24 Years 至 85 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • An eligible patient to be entered into the Registry is defined as:
  • Patient with advanced breast cancer.
  • Halaven was given or has been treating during the period of 1 Jan 2015 to 31 Dec
  • Halaven was given as single or combination.
  • Patient received at least one cycle treatment (a 21-day cycle or 2 doses) of Halaven.
  • Patient with at least 80% of the required information of the Registry CRF to be entered. It will be calculated automatically by the Registry system.
  • Patient to be selected for the Registry will be based on chorological order of a patient occurred in a study center during the defined period of the Registry, if all other eligibility criteria are met.

排除标准

  • Those who not meet the inclusion criteria will be excluded.

结局指标

主要结局

Disease Control Rate (DCR)

时间窗: 24 months

he percentage of patients with advanced or metastatic cancer who have achieved complete response, partial response and stable disease to a therapeutic intervention

次要结局

  • Number of patients with adverse events(24 months)

研究者

发起方
Chang Gung Memorial Hospital
申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验