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临床试验/NCT05871307
NCT05871307进行中(未招募)不适用

Neoadjuvant vs. Intraoperative vs. Adjuvant Resection Cavity Radiotherapy of Brain Metastases - A Prospective Randomized Explorative Phase II Trial

University Hospital Heidelberg2 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2024年2月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
90
试验地点
2
主要终点
Assessment of treatment response

研究概览

简要总结

Patients suffering from malignancies in advanced stages often develop brain metastases, which limit both the life span and the quality of life.

Combining surgery and radiotherapy for resectable brain metastases is standard of care but there is a lot of controversy on which kind of radiotherapy is best suitable. Recently, first volumetric in-silico analyses point to theoretical advantages of neoadjuvant stereotactic radiotherapy of brain metastases. Special about this trial is the direct comparison between the three currently discussed radiotherapy options for resectable brain metastases: Neoadjuvant stereotactic radiotherapy, intraoperative radiotherapy and adjuvant stereotactic radiotherapy.

详细描述

This trial approach allows for detailed comparison of resected tissue samples, cerebrospinal fluid and blood of all patient groups. So, the investigators will investigate biomaterial of recently irradiated (neoadjuvant and intraoperative arms) and non-irradiated (adjuvant arm) tissue. All this prompts the main issues of the explorative randomized controlled phase 2 RADCAV trial: Is there a difference between neoadjuvant stereotactic radiotherapy vs. intraoperative radiotherapy vs. adjuvant stereotactic radiotherapy regarding the factors immune profiling, dosimetry, efficacy and toxicity. It can be hypothesized that the resected tissue differs between recently irradiated and non-irradiated brain metastases, for example regarding different histopathologic and molecular pathologic markers including immune environment, markers for cell death and markers for tumor invasion. Are there histopathologic and molecular pathologic markers of tumor cell response and prognosis so the investigators can better understand the effects of irradiation on metastatic brain tissue? And are there relevant differences in dosimetry that put patients at different risks for efficacy and toxicity?

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

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

  • Histologically confirmed solid malignancy
  • Metastatic brain disease (1-10 brain metastases), with at least one brain metastasis in a non-eloquent location (i.e. motor or speech) planned for resection
  • Maximum size of the brain metastasis <5cm
  • Eligibility of patients for both stereotactic radiotherapy and resection
  • Time interval from resection to adjuvant stereotactic radiosurgery of 2-6 weeks
  • Time interval from neoadjuvant stereotactic radiosurgery to resection of 1-7 days
  • Possibility to postpone resection for neoadjuvant stereotactic radiosurgery, if applicable
  • Karnofsky performance scores >= 70 or Eastern Cooperative Oncology Group (ECOG) >= 2 at enrollment
  • Age ≥ 18 years of age
  • For women with childbearing potential, (and men) adequate contraception.
  • Ability of subject to understand character and individual consequences of the clinical trial
  • Written informed consent (must be available before enrolment in the trial)

排除标准

  • Necessity of immediate surgical resection due to life threatening symptoms
  • brain metastasis directly located (≤10mm) next to the optic system or brain stem
  • Refusal of the patients to take part in the study
  • Small-cell lung cancer (SCLC) or hematologic malignancy as primary malignant illness
  • Leptomeningeal disease suspected RadCav Trial Protocol Version 1.1, 01.07.2022 18
  • Previous radiotherapy of the brain
  • Contraindication for contrast-enhanced MRI
  • Pregnant or lactating women
  • Participation in another competing clinical study or observation period of competing trials, respectively

研究组 & 干预措施

Experimental Arm A (Preoperativ SRS)

Experimental

Preoperative stereotatic radiosurgery following resection of brain metastases after 1-7 days

干预措施: Preoperative Radiotherapy (Radiation)

Standard Treatment Arm C (Posoperativ SRS)

Active Comparator

Resection of brain metastases following stereotactic radiotherapy after 2-6 weeks

干预措施: Postoperative Radiotherapy (Radiation)

Experimental Arm B (Intraoperativ SRS)

Experimental

Intraoperative stereotactic radiotherapy after resection of brain metastases

干预措施: Intraoperative Radiation (Radiation)

结局指标

主要结局

Assessment of treatment response

时间窗: through study completion, an avarage of 60 month

number of patients without progresion according to RANO-BM

local tumor control

时间窗: through study completion, an avarage of 60 month

events of tumor progression or recurrence in the area of 1cm surrounding the resection cavity and surrounding the surgical access

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Juergen Debus

Department Director

University Hospital Heidelberg

研究点 (2)

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