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临床试验/NCT05124236
NCT05124236招募中不适用

A Multicenter Prospective, Interventional, Randomized Trial of Preoperative Radiosurgery Compared With Postoperative Stereotactic Radiotherapy for Resectable Brain Metastases

Susanne Rogers10 个研究点 分布在 3 个国家目标入组 200 人开始时间: 2022年7月29日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
200
试验地点
10
主要终点
Leptomeningeal disease

研究概览

简要总结

The research question is whether a single fraction of preoperative radiosurgery can reduce the incidence of leptomeningeal disease 12 months following resection of a brain metastasis (BM) as compared with 5 fractions of postoperative stereotactic radiotherapy.

详细描述

Neurosurgical resection of a brain metastasis in patients with a diagnosis of cancer may be indicated however the recurrence rate approximates 50% and adjuvant radiotherapy is standard. Single fraction postoperative stereotactic radiosurgery (SRS) has been widely adopted as a standard therapy as it achieves equivalent survival and prevents loss of neurocognitive function as compared with whole brain radiotherapy and improves cavity local control rates as compared with observation. Hypofractionated stereotactic radiotherapy in 3 to 5 fractions (hfSRT) is also used in the postoperative setting.

Nodular leptomeningeal disease (nLMD) is a recognised pattern of failure after postoperative SRS and hfSRT. A 16.9% incidence of nodular LMD was seen after surgery and a similar incidence of 11%-28%is reported following postoperative SRS in retrospective series. These data suggest that postoperative SRS/hfSRT have no significant effect on the development of LMD following surgery.

The incidence of LMD following single fraction preoperative SRS is only 6.1% according to the largest retrospective series. Preoperative SRS takes advantage of the easier delineation of an intact BM and sterilizes tumor cells disseminated at surgery. Side effects are minimized by a smaller planning margin, a dose reduction and resection of the irradiated volume. In addition, there is no delay to systemic therapy due to wound healing/complications. Furthermore, a single fraction offers patient convenience.

This trial will randomise and compare intracranial outcomes between single fraction preoperative SRS and 5 fraction postoperative hFSRT.

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

  • Provision of signed and dated informed consent form
  • Stated willingness to comply with all study procedures and availability for the duration of the study
  • Karnofsky performance status ≥60
  • Histological diagnosis of a malignant primary or metastatic tumour
  • Ability to take steroids
  • No contraindication to magnetic resonance imaging (MRI)
  • MRI-diagnosis of a clearly demarcated contrast-enhancing brain metastasis up to 4.0 cm diameter indicated for neurosurgical resection (tumorboard decision). Up to 3 other brain metastases suitable for primary radiosurgery/ stereotactic radiotherapy
  • Survival estimated by primary clinician > 12 months
  • Platelet count > 100/ml, INR < 1.3, Hb > 7.5 g/dL

排除标准

  • Radiosensitive histology: germ cell tumour, lymphoma, multiple myeloma
  • >10 mm midline shift, effacement of the 4th ventricle or other sign of raised intracranial pressure requiring urgent decompressive surgery
  • More than 4 brain metastases or the diameter of the metastasis for resection >4.0 cm.
  • More than 1 metastasis requiring resection
  • Leptomeningeal disease in the CSF or on MRI (unless localized and can be irradiated then resected with the metastasis)
  • Prior radiation to the brain (SRS/SRT to lesion to be resected and /or WBRT)
  • Prior resection of a primary or secondary brain tumor
  • Prior diagnosis of a non-meningioma brain tumor
  • Prior radionuclide therapy within 30 days
  • Prior anti-VEGF therapy within 6 weeks
  • Unable to tolerate radiosurgery immobilization and treatment
  • Inability to give informed consent
  • Pregnancy or lactation
  • Females of reproductive potential not willing to use effective contraception for at least 6 months after radiotherapy
  • Males of reproductive potential not effective contraception for 3 months after radiotherapy
  • Lack of likely compliance with protocol and follow-up

研究组 & 干预措施

Preoperative radiosurgery

Experimental

The interventional arm is single fraction preoperative radiosurgery to a brain metastasis identified for neurosurgical resection.

干预措施: preoperative radiosurgery (Radiation)

Postoperative hypofractionated stereotactic radiotherapy

Active Comparator

The active comparator arm is the standard of care of postoperative hypofractionated stereotactic radiotherapy to the surgical cavity in 5 fractions following resection of the brain metastasis.

干预措施: postoperative hypofractionated stereotactic radiotherapy (Radiation)

结局指标

主要结局

Leptomeningeal disease

时间窗: 12 months after intervention

time to leptomeningeal disease

次要结局

  • Distant brain failure(12 months after intervention)
  • Quality of life assessment(3,6,12 months after intervention)
  • Radionecrosis(12 months after intervention)
  • Local control of the surgical cavity(12 months after intervention)

研究者

发起方
Susanne Rogers
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Susanne Rogers

Sponsor-Investigator

Kantonsspital Aarau

研究点 (10)

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