Non-small cell lung cancer
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1)Patients aged 16 years or older 2)Patients with pathologically (histology or cytology) confirmed non-small cell lung cancer (NSCLC) 3)Patients who have received one or more drug regimens for lung cancer. Patients with treatment-naive NSCLC can be enrolled if blood sample is submitted. (Preoperative/postoperative adjuvant chemotherapy is not included in the calculation of the number of regimens. Chemoradiotherapy is included in the calculation of the number of regimens.) 4)Eastern Cooperative Oncology Group performance status (PS) of 0 or 2 5)Patients who are expected to live for at least 3 months from the date of study enrollment 6)Patients who are able to submit samples that can be used for genetic analyses. 7)Patients who consider to enroll in genotype-directed clinical trials if the target gene alterations are identified in this study 8)Patients who have provided written consent to enroll in this study
Exclusion criteria
Exclusion criteria: none
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To characterize the clinicopathological and molecular biological features of lung cancer with genetic alterations identified in the genomic screening. | — |
Countries
Japan
Contacts
National Cancer Center Hospital East Department of Thoracic Oncology