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Phase I/II study of Gefitnib monotherapy as neo-adjuvant chemotherapy for cN2 lung adenocarcinoma with the EGFR mutatio

Not Applicable
Conditions
lung adenocarcinoma
Registration Number
JPRN-UMIN000004807
Lead Sponsor
KantoKoshinetsu lung cancer research group
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
20
Inclusion Criteria

Not provided

Exclusion Criteria

(1) patients who has interstitial pneumonia identified by chest CT or by blood test (2) (3) Patients with EGFR mutation (T790M) which is NOT expected the good response with gefitinib. (4) Patients with uncontrollable complications (5) Pregnant or lactation women, or women with known or suspected pregnancy (6) Patients with severe malabsorption syndrome or with severe functional gastrointestinal disorder (7) patients with systemic administration steroids over 4 weeks (8) Patients with contraindication of gefitinib (9) Patients with active concomitant malignancy (10) Inappropriate patients for this study judged by the physicians

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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