Study of EGFR-TKI to Asymptomatic Brain Metastases of NSCLC
Conditions
Asymptomatic Brain Metastases of Non Small Cell Lung Cancer
Conditions: official terms
Brain Neoplasms - Carcinoma, Non-Small-Cell Lung - Neoplasm Metastasis
Conditions: Keywords
EGFR mutations, asymptomatic brain metastases, EGFR-TKI, Erlotinib
Study Type
Interventional
Study Phase
Phase 2
Study Design
Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Intervention
Name: EGFR-TKI
Type: Drug
Overall Status
Not yet recruiting
Summary
The purpose of this study is to determine whether EGFR-TKI can control the development of intracranial lesions in Non Small Cell Lung Cancer patients with asymptomatic brain metastases, and the difference in progression free survival between exon 19 and exon 21 mutations.
Detailed Description
A open, positive control of phase II clinical trials, divided into selection period, treatment period and follow-up period , comply with the standard set of participants signed a written informed consent, according to different divided into 19 patients with EGFR mutations outside show son mutation group) and 21 extra show mutations, and according to the ECOG physical status, age, previous systemic treatments such as hierarchical analysis, regular follow-up and to assess efficacy, life care and safety.
Criteria for eligibility
Healthy Volunteers: No
Maximum Age: 70 Years
Minimum Age: 18 Years
Gender: Both
Criteria: Inclusion Criteria:

1. at the age of 18 -70 years old, male or female

2. the non-small cell lung cancer diagnosed by histopathology

3. detected by ARMS to confirm that the EGFR sensitive mutant patients

4. the existence of MRI diagnosis of intracranial metastatic head enhancement, and the presence of imaging evaluating lesions (according to RECIST1.1)

5. have not received prior treatment of intracranial metastases, including radiotherapy, gamma knife, chemotherapy drugs

6. no brain metastasis symptoms, including, increased intracranial pressure, no vomiting, ignoring the papillary edema, no headache, without hemiplegia, ignore things not clear, without epilepsy

7. PS:0 or 1

8. the expected survival time 3 months >

9. patients signed informed consent voluntarily

Exclusion Criteria:

1. 4 weeks before entering the group received operation or operation, the wound has not healed completely

2. into group 2 weeks before receiving immune therapy or treatment of traditional Chinese Medicine

3. serious cardiovascular diseases, including Department of internal medicine, uncontrolled hypertension, unstable angina, myocardial infarction history exists within the past June, severe arrhythmia or pericardial effusion

4. serious infection, need intravenous antibiotic, antifungal or antiviral treatment

5. before entering the group 4 weeks participated in any study drug clinical trial

6. there are serious tumor invasion, oppression by the main bronchus or bronchial stenosis or obstruction, superior vena cava syndrome

7. the existence of herniation of brain tumor apoplexy, epilepsy, and frequent

8. suffering from a mental illness, poor compliance

9. the researchers think that do not fit into the group of cases
Location
Start Date
January 2015
Completion Date
January 2017
Sponsors
Wuhan Union Hospital, China
Source
Wuhan Union Hospital, China
Record processing date
ClinicalTrials.gov processed this data on July 28, 2015
ClinicalTrials.gov page