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临床试验/NCT02421718
NCT02421718招募中不适用

Standard Follow-up Program (SFP) for Lung Cancer Patients Treated With Radiotherapy or Chemoradiation

University Medical Center Groningen1 个研究点 分布在 1 个国家目标入组 10,000 人开始时间: 2013年3月最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
10,000
试验地点
1
主要终点
Acute toxicity

研究概览

简要总结

Motive:

In order to improve the treatment technique, a comprehensive follow-up program is needed to obtain all relevant patient, treatment and toxicity data from lung cancer patients.

Goal:

To set-up and maintain a database containing treatment results in terms of tumor control, side effects, complications and patient-reported quality of life.

A standard database of patients receiving photon treatment will be created. These data are then linked to dose-volume data of radiotherapy, with the aim to build prediction models for both tumor control and toxicity after radio (chemo) therapy that can later be used for selecting patients for proton treatment.

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

  • Patients with NSCLC or SCLC-LD or thymoma or lung metastases (treated with stereotactic radiotherapy)
  • Patients receiving radiotherapy dose > 40 Gy

排除标准

  • Failure to comply with any of the inclusion criteria

结局指标

主要结局

Acute toxicity

时间窗: Highest during and within 2 weeks after last day of radiation therapy

esophagitis (Common Terminology Criteria for Adverse Events, version 4.0)

Late toxicity

时间窗: Highest within one year after last day of radiation therapy

esophagitis (Common Terminology Criteria for Adverse Events, version 4.0); pneumonitis (Common Terminology Criteria for Adverse Events, version 4.0)

次要结局

  • Loco-regional tumor control(at 3 years after first day of radiation therapy)
  • Overall survival(at 5 years after first day of radiation therapy)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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