Clinical Efficacy and Safety of EGFR-TKI Combined With Nimotuzumab in the Treatment of Leptomenin… (NCT04833205) | Clinical Trial Compass
UnknownPhase 2
Clinical Efficacy and Safety of EGFR-TKI Combined With Nimotuzumab in the Treatment of Leptomeningeal Metastases From Lung Cancer
China30 participantsStarted 2021-04-19
Plain-language summary
Clinical Efficacy and Safety of EGFR-TKI Combined With Nimotuzumab in the Treatment of Leptomeningeal Metastases From Lung Cancer.
Who can participate
Age range18 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* age 18 years or older, gender not limited;
* A definite diagnosis of Leptomeningeal metastases from lung cancer, including cerebrospinal fluid cytology and/or neuroimaging;
* Have a clear history of lung cancer, including histopathological diagnosis, or cytopathology combined with imaging diagnosis
* Patients who received any of EGFR inhibitors (gefitinib, erlotinib, afatinib, osimertinib etc.) meet the diagnostic criteria for secondary resistance and were in a slow progression stage
* Detection results of cerebrospinal fluid, blood gene or lung tissue specimens showed EGFR mutation, and immunohistochemistry results of cerebrospinal fluid, blood gene or lung tissue showed positive EGFR expression
* Bone marrow, liver, kidneys and blood clotting function are relatively stable
Exclusion Criteria:
* Eastern Cooperative Oncology Group scored \> 2 points
* Patients had poor compliance, or for other reasons the investigator considered them unsuitable to participate in the study