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A prospective observational study of osimertinib as predictive marker against patients with EGFR T790M-positive NSCLC.

Not Applicable
Conditions
ung Cancer
Registration Number
JPRN-UMIN000027233
Lead Sponsor
Gunma University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Sex
All
Target Recruitment
45
Inclusion Criteria

Not provided

Exclusion Criteria

1)Active double cancer 2)Interstitial pneumonitis on chest CT 3)Symptomatic brain metastases 4)Uncontrollable pleural effusion or pericardial effusion 5)Active infectious disease 6)No allogeneic bone marrow transplant

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Primary endpoint:To predict the efficacy of osimertinib according to quantitative amount of T790M expression. Secandary endpoint:To predict the efficacy of osimertinib according to quantitative amount of C797S.
Secondary Outcome Measures
NameTimeMethod
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