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临床试验/NL-OMON51261
NL-OMON51261招募中不适用

Immunological and molecular effects of MR-guided stereotactic radiotherapy in adrenal metastases - A hypothesis generating trial (IM-SABR) - IM-SABR

Vrije Universiteit Medisch Centrum0 个研究点目标入组 30 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
30

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 至 99(—)

入选标准

  • In order to be eligible to participate in this study, a subject must meet all
  • of the following criteria:
  • 1. Have adrenal metastases, for which MR-guided SABR has been recommended
  • following dis-cussions within a multi-disciplinary tumor board.
  • 2. Be willing and able to provide written informed consent for the trial.
  • 3. Be 18 years of age on day of signing informed consent.

排除标准

  • 1. Has a diagnosis of immunodeficiency or is receiving systemic steroid therapy
  • or any other form of immunosuppressive therapy within 30 days prior to the
  • MR-guided SABR.
  • 2. Has had prior chemotherapy, targeted small molecule therapy, or radiotherapy
  • within 30 days prior to MR-guided SABR.
  • 3. Has a known additional malignancy that is progressing or requires active
  • treatment. Exceptions include basal cell carcinoma of the skin, squamous cell
  • carcinoma of the skin, or in situ cervical cancer that has undergone
  • potentially curative therapy.
  • 4. Has an active autoimmune disease requiring systemic treatment within the
  • past 3 months or a syndrome that requires systemic steroids or
  • immunosuppressive agents. Subjects that require intermittent use of
  • bronchodilators or local steroid injections would not be excluded from the
  • study. Subjects with hypothyroidism stable on hormone replacement will not be
  • excluded from the study.
  • 5. Has an active infection requiring systemic therapy.
  • 6. Has a history or current evidence of any condition, therapy, or laboratory
  • abnormality that might confound the results of the trial, interfere with the
  • subject*s participation for the full du-ration of the trial, or is not in the
  • best interest of the subject to participate, in the opinion of the treating
  • investigator.
  • 7. Has a known history of Human Immunodeficiency Virus (HIV) (HIV 1/2
  • antibodies) or a known active Hepatitis B (e.g., HBsAg reactive) or Hepatitis C
  • (e.g., HCV RNA [qualitative] is detected).

研究者

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