Skip to content

Clinical efficacy of nimotuzumab combined with EGFR TKIs and EGFR TKIs in the treatment of meningeal metastasis of lung cancer

Clinical efficacy of nimotuzumab combined with EGFR TKIs and EGFR TKIs in the treatment of meningeal metastasis of lung cancer

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000039917
Enrollment
Unknown
Registered
2020-11-14
Start date
2020-12-01
Completion date
Unknown
Last updated
2021-06-14

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

Conditions

Leptomeningeal metastasis

Interventions

group 1:???????EGFR-TKIs ???????EGFR-TKIs 16/2000 Nimotuzumab combined with EGFR-TKIs
group2 :EGFR-TKIs alone

Sponsors

The Second Hospital of Hebei Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients with clear diagnosis of meningeal metastasis of lung cancer, including cytological diagnosis of cerebrospinal fluid and neuroimaging diagnosis; 2. Patients with a clear history of lung cancer: including histopathological diagnosis, or cell pathology combined with imaging diagnosis; 3. Patients aged 18-75 years old; 4. Subjects without severe abnormal liver and kidney function; blood routine examination showed that WBC was not less than 4.0 x 1012 and platelet was not less than 100 x 10^9; 5. Patients with no previous history of serious nervous system diseases; 6. Subjects without severe heterogenous state.

Exclusion criteria

Exclusion criteria: 1. Patients receiving other targeted drugs in addition to EGFR-TKI within 2 months, such as recombinant human endostatin, crizotinib, trastuzumab, etc.; 2. Subjects with ECoG score > 2 and neurological failure, including severe encephalopathy, imaging examination showed 3-4 degrees of white matter lesions, moderate or above coma, GCS score less than 9; 3. Patients with extensive and fatal systemic tumor progression and lack of effective treatment; 4. Patients with poor compliance or not suitable for the study due to other reasons.

Design outcomes

Primary

MeasureTime frame
the rate of PFS;

Countries

China

Contacts

Public ContactBu Hui

The Second Hospital of Hebei Medical University

buhuimy1@163.com+86 13831106903

Outcome results

None listed

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