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临床试验/NCT05583409
NCT05583409尚未招募不适用

Effect of SBRT Combined With Osimertinib Compared With Osimertinib Alone for Stage IV Non-small Cell Lung Cancer

Li Zhang1 个研究点 分布在 1 个国家目标入组 72 人开始时间: 2023年1月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
72
试验地点
1
主要终点
PFS

研究概览

简要总结

This is a Prospective, Multicenter, Randomized Controlled study to evaluate Stereotactic Body Radiation Therapy (SBRT) as a potential treatment for stage IV non-small cell lung cancer (NSCLC) that has a mutated epidermal growth factor receptor (EGFR) and has been receiving treatment with Osimertinib

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 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients must have biopsy proven metastatic NSCLC (Stage IV).
  • Patients receiving first-line Osimertinib for EGFR mutant-positive for 3 months and achieved stable disease or partial response.
  • Age 18 to 75 years old.
  • Patients must have measurable disease at baseline.
  • The amount of metastatic focus <
  • ECOG score 0-2 7 Adequate normal organ and marrow function for TKI treatment and radiotherapy.
  • Patients must has sensitizing EGFR mutation (e.g. exon 19 deletion or exon 21 L858R)
  • Patients must provide written informed consent to participate in the study.

排除标准

  • Patients who previously received radiotherapy to the primary site.
  • Patient can't tolerate radiotherapy or targeted therapy;
  • Pregnant or nursing women

研究组 & 干预措施

Osimertinib plus SBRT

Experimental

SBRT with photon and dose is 40Gy/5F after three months after Osimertinib treatment

干预措施: SBRT+Osimertinib (Radiation)

Osimertinib

Active Comparator

Osimertinib 80mg, po, Qd

干预措施: Osimertinib 80 MG (Drug)

结局指标

主要结局

PFS

时间窗: 2 years

the time from the beginning of Osimertinib treatment to disease progression or death

次要结局

  • OS(3 years)

研究者

发起方
Li Zhang
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Li Zhang

Professor

Tongji Hospital

研究点 (1)

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