Non-small cell lung cancer
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Histologically or cytologically diagnosed NSCLC 2. Clinical stage II, III or IV 3. Eastern Cooperative Oncology Group performance status (PS) of 0 or 1 4. Adequate function of main organ that meets the following criteria -1 Neutrophil count>=1500/mm3 -2 Hemoglobin>=8.0g/dL -3 Platelet count>=7.5*104/mm3 -4 AST,ALT<=upper limit of normal *2.5 5 Serum bilirubin <=upper limit of normal *1.5 mg/dL 5. Other serious medical complications (interstitial pneumonitis, uncontrolled diabetes mellitus, heart failure, active infectious disease etc.) 6. Life expectancy more than 3 months 7. Materials available for genome analysis 8. Declaring enrollement of clinical trial through genome analysis 9. Written informed consent
Exclusion criteria
Exclusion criteria: none
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To clarify the clinicopathological and molecular feature in RET fusion-positive lung cancer | — |
Countries
Japan
Contacts
National Cancer Center Hospital East Division of Thoracic Oncology