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临床试验/NCT03741673
NCT03741673进行中(未招募)3 期

A Phase III Trial of Pre-Operative Stereotactic Radiosurgery (SRS) Versus Post-Operative SRS for Brain Metastases

M.D. Anderson Cancer Center1 个研究点 分布在 1 个国家目标入组 180 人开始时间: 2018年11月8日最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
进行中(未招募)
入组人数
180
试验地点
1
主要终点
Leptomeningeal disease (LMD)-free rate

研究概览

简要总结

This phase III trial studies stereotactic radiosurgery (SRS) before surgery to see how well it works compared with SRS after surgery in treating patients with cancer that has spread to the brain (brain metastases). SRS is the delivery of focused, high-dose radiation given in a single session to the tumors, with a minimal dose given to uninvolved areas of the brain.

详细描述

PRIMARY OBJECTIVE:

I. To investigate the 1 year leptomeningeal disease (LMD)-free rate among patients with surgically resectable metastatic brain lesions randomized to post-operative stereotactic radiosurgery (SRS) (standard care) versus pre-operative SRS followed by surgery (experimental arm).

SECONDARY OBJECTIVE:

I. To investigate the local control (LC), distant brain metastasis rate, overall survival (OS) of pre-operative (pre-op) versus (vs) post-operative (post-op) SRS in patients with brain metastasis.

EXPLORATORY OBJECTIVES:

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
否

入选标准

  • •The primary lesion pre-operatively can have a maximum diameter of =< 4 cm for single fraction and =< 7 cm for multifraction therapy
  • •Patients must be considered candidates for SRS within +/- 30 days of surgical resection as defined by either history and physical (H&P) or presentation at brain metastasis tumor board conference note
  • •Patients must have a Karnofsky performance scores >= 70 or Eastern Cooperative Oncology Group (ECOG) >= 2 within 30 days of enrollment
  • •Patients must agree to randomization as documented by signing the Institutional Review Board (IRB) approved consent form
  • •No radiographic evidence of leptomeningeal disease on MD Anderson Cancer Center (MDACC) departmental radiology report or study neuro-radiologist review
  • •Documented history of malignancy

排除标准

  • •Patients who have received prior radiation therapy to the brain for any reason
  • •The primary tumor is small-cell lung cancer, lymphoma, leukemia, or multiple myeloma
  • •For females, if they are pregnant or breast-feeding (The exclusion is made because gadolinium may be teratogenic in pregnancy)

研究组 & 干预措施

Group I (pre-operative SRS)

Experimental

Patients undergo SRS within 30 days of randomization followed by surgery within 30 days. Patients may undergo additional SRS if disease returns after treatment.

干预措施: Stereotactic Radiosurgery (Radiation)

Group II (post-operative SRS)

Active Comparator

Patients undergo surgery within 30 days of randomization followed by standard of care SRS within 30 days. Patients may undergo additional SRS if disease returns after treatment.

干预措施: Quality-of-Life Assessment (Other)

Group I (pre-operative SRS)

Experimental

Patients undergo SRS within 30 days of randomization followed by surgery within 30 days. Patients may undergo additional SRS if disease returns after treatment.

干预措施: Quality-of-Life Assessment (Other)

Group I (pre-operative SRS)

Experimental

Patients undergo SRS within 30 days of randomization followed by surgery within 30 days. Patients may undergo additional SRS if disease returns after treatment.

干预措施: Questionnaire Administration (Other)

Group II (post-operative SRS)

Active Comparator

Patients undergo surgery within 30 days of randomization followed by standard of care SRS within 30 days. Patients may undergo additional SRS if disease returns after treatment.

干预措施: Questionnaire Administration (Other)

Group II (post-operative SRS)

Active Comparator

Patients undergo surgery within 30 days of randomization followed by standard of care SRS within 30 days. Patients may undergo additional SRS if disease returns after treatment.

干预措施: Stereotactic Radiosurgery (Radiation)

结局指标

主要结局

Leptomeningeal disease (LMD)-free rate

时间窗: At 1 year

Aalen-Johansen estimates will be used for LMD. Uni- and multi-variable analysis of time to LMD will be done using Fine-Gray proportional hazards regression. Model assumptions will be verified graphically by residual analyses.

次要结局

  • Distant brain control(At 1 year)
  • Local control rate(At 1 year)
  • Overall survival (OS)(At 1 year)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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