跳至主要内容
临床试验/NCT01220934
NCT01220934已完成不适用

Clinical Practice Surveillance of the Use of Herceptin in Patients With HER2-positive Advanced Adenocarcinoma of the Stomach or Gastro-esophageal Junction (GEJ) (HERMES)

Hoffmann-La Roche1 个研究点 分布在 1 个国家目标入组 443 人开始时间: 2010年4月16日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
443
试验地点
1
主要终点
Response rate according to Response Evaluation Criteria in Solid Tumors (RECIST)

研究概览

简要总结

This observational, multicenter study will assess the efficacy and safety of Herceptin (trastuzumab) in routine clinical practice in patients with HER2-positive advanced adenocarcinoma of the stomach or gastro-esophageal junction. Data from patients will be collected for approximately 12 months.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • Adult patients, >/=18 years of age
  • Histologically confirmed advanced adenocarcinoma of the stomach or gastro-esophageal junction (GEJ) with locally advanced and/or metastatic disease
  • HER2-positive tumor
  • Patients who are eligible for treatment with Herceptin according to the judgment of the physician

排除标准

  • Unwilling or unable to sign informed consent form
  • Any contraindications, interactions and incompatibilities to Herceptin

结局指标

主要结局

Response rate according to Response Evaluation Criteria in Solid Tumors (RECIST)

时间窗: 12 months

Progression-free survival according to Response Evaluation Criteria in Solid Tumors (RECIST)

时间窗: 12 months

Overall survival according to Response Evaluation Criteria in Solid Tumors (RECIST)

时间窗: 12 months

次要结局

  • Documentation of the testing process for HER2-positive tumors(12 months)
  • Assessment of implementation of guidelines and recommendations of Herceptin administration in routine clinical practice(12 months)
  • Documentation of backbone chemotherapy treatment and concomitant medication(12 months)
  • Quality of Life questionnaire(12 months)
  • Surveillance of weight change(12 months)
  • Safety (incidence of adverse events)(12 months)
  • Surveillance of pain intensity and analgesic consumption(12 months)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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