跳至主要内容
临床试验/DRKS00026665
DRKS00026665招募中不适用

Prospective evaluation of the safety and efficacy of MR-guided moderately hypofractionated radiotherapy for inoperable malignant tumors of the lung, pleura, and mediastinum with a diameter > 5 cm and poor risk factors - MR-HYPOLUNG - MR-HYPOLUNG

Klinik und Poliklinik für Strahlentherapie und Radioonkologie, Klinikum Grosshadern der LM0 个研究点目标入组 10 人开始时间: 2021年11月8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
10

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 Years 至 one(—)
性别
All

入选标准

  • 1. Histologically confirmed, inoperable tumor of the lung, pleura or mediastinum with a diameter > 5 cm.
  • 2. Age = 18 years
  • 3. Limited pulmonary function and reserve (FEV = 1L and/or DLCO <40% or long-term oxygen therapy).
  • 4. ECOG Performance Status = 2
  • 5. Prior surgery, systemic and local ablative therapies (RFA, SABR, brachytherapy, etc.) are allowed.
  • 6. Indication for radiotherapy confirmed at the multidisciplinary tumor board.
  • 7. Patients are able to understand and willing to sign an IRB-approved informed consent document and adhere to the conditions of the study

排除标准

  • 1. Known contraindications for radiotherapy e.g. severe comorbidities, interstitial lung disease etc.
  • 2. Significant overlap with a previously treated radiation volume - prior radiotherapy is generally allowed as long as all dose requirements are met in the composite plan (biologically effective doses are calculated for this purpose).
  • 3. Pregnant and/or breastfeeding.
  • 4. Medical or psychological impairments that do not allow proper informed consent or trial participation.
  • 5. Lack of legal capacity.

研究者

发起方
Klinik und Poliklinik für Strahlentherapie und Radioonkologie, Klinikum Grosshadern der LM

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