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临床试验/NCT07317245
NCT07317245招募中不适用

HUmanitas PROtontherapy (HU-PRO)

Istituto Clinico Humanitas1 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2026年1月12日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
500
试验地点
1
主要终点
collecting real world data

研究概览

简要总结

Proton therapy is a cancer treatment, similar to the more commonly used radiation therapy. It uses radiation to destroy cancer cells and helps control the disease in the treated area.

However, when proton therapy is compared with standard radiation therapy, many studies show fewer side effects and better disease control. This is due to the unique physical properties of the particles used in proton therapy.

At present, in Italy, this innovative treatment is available only for selected diseases, as defined by national guidelines. For this reason, it is very important to collect as much data as possible to support the further development of proton therapy and to improve treatment safety and effectiveness.

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

  • Solid tumors candidate to proton therapy, in particular, according to Italian regolamentations
  • Written informed consent for HU-PRO according to applicable legal and ethical requirements
  • Indication for proton therapy
  • ≥ 18 years old
  • ECOG PS (performance status scale) 0-2

排除标准

  • Age < 18 years old
  • ECOG (performance status scale) >3
  • Life expectancy < 3 months
  • Inability to provide informed consent

研究组 & 干预措施

proton therapy

all patients treated with proton therapy according to clinical practice

结局指标

主要结局

collecting real world data

时间窗: from enrollment to 10 years

To collect real-world data on cancer patients treated with protonherapy, to support research and to provide evidence of the role of protontherapy in a multidisciplinary approach.

次要结局

  • identify prognostic biomarkers(from enrollment to 10 years)
  • toxicities profiles(from enrollment to 10 years)
  • Secondary Cancer Risk(from enrollment to 10 years)
  • Optimize treatment plannig(from enrollment to 10 years)
  • Asses Outcomes in Rare or Radioresistant Tumors(from enrollment to 10 years)
  • Analyze Quality of Life Outcomes(from enrollment to 10 years)
  • Monitor Treatment Adherence and Compliance(from enrollment to 10 years)

研究者

发起方
Istituto Clinico Humanitas
申办方类型
Other
责任方
Sponsor

研究点 (1)

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