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Evaluation of different treatment methods for brain metastasis of NSCLC

Evaluation of different treatment methods for brain metastasis of NSCLC

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000036392
Enrollment
Unknown
Registered
2020-08-22
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Brain metastasis of NSCLC

Interventions

conventional group:Surgery+conventional therapy(Radiotherapy)
novel group:Surgery+Targeted/immune therapy

Sponsors

Huashan Hospital Affiliated to Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients with non-small cell lung cancer diagnosed; 2. Imaging of brain metastases, patients with lesion size > 1.5cm * 1.5cm * 1.5cm; 3. Patients who had no operation contraindication and underwent total resection of metastatic tumor; 4. Patients with NSCLC brain metastases confirmed by pathology; 5. Subjects with or without other treatments (radiotherapy, targeted therapy, immunotherapy); 6. Patients aged over 18 years and less than 65 years, both male and female; 7. Subjects signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with a history of other primary tumors; 2. Patients with primary brain diseases: encephalitis, meningoencephalitis, brain parasite infection, brain trauma, massive cerebral infarction, cerebral hemorrhage, subarachnoid hemorrhage; 3. Patients with severe cardiopulmonary disease: COPD, interstitial pneumonia, coronary heart disease, heart failure; 4. Patients with abnormal liver and kidney function: serum creatinine >= 1.25 times of normal upper limit, creatinine clearance rate = 1.5 times of normal upper limit, AST and alt >= 2.5 times of normal upper limit; 5. Pregnant or lactating objects; 6. Subjects participated in other clinical studies at the same time.

Design outcomes

Primary

MeasureTime frame
PFS;OS;

Secondary

MeasureTime frame
annual survival rate;

Countries

China

Contacts

Public ContactXu Hongzhi

Huashan Hospital Affiliated to Fudan University

xuhongzhi95@sina.com+86 13651932866

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026