Clinical Research Directory

Inclusion Criteria: 1. Cohort 1: Female or male aged \>=18 years; 2. Cohort 1: Received neoadjuvant treatment with Ensartinib before the project started; 3. Cohort 1: Diagnosed with clinical stage II-III resectable or potentially resectable (T1-4 N2 M0) ALK-positive NSCLC before neoadjuvant treatment; 4. Cohort 1: Confirmed ALK positive by immunohistochemistry (IHC), fluorescence in situ hybridization (FISH), next-generation sequencing (NGS), or other non-specific sequencing methods before receiving ALK inhibitor therapy. 5. Cohort 2: Female or male aged \>=18 years; 6. Cohort 2: Intended to receive Ensartinib monotherapy as neoadjuvant treatment for 6-12 weeks; 7. Cohort 2: Diagnosed with clinical stage II-III resectable or potentially resectable (T1-4 N2 M0) ALK-positive NSCLC before neoadjuvant treatment; 8. Cohort 2: Confirmed ALK positive by immunohistochemistry (IFL), fluorescence in situ hybridization (FISH), next-generation sequencing (NGS), or other non-specific sequencing methods before receiving ALK inhibitor therapy; 9. Cohort 2: Signed informed consent form; 10. Cohort 3: Female or male aged \>=18 years; 11. Cohort 3: Intended to receive neoadjuvant treatment including Ensartinib, but not meeting the inclusion criteria for Cohort 2; 12. Cohort 3: Diagnosed with clinical stage II-III resectable or potentially resectable ALK-positive NSCLC before neoadjuvant treatment; 13. Cohort 3: Confirmed ALK positive by immunohistochemistry (IHC), fluorescence in situ hybridization (FISH), next-generation sequencing (NGS), or other non-specific sequencing methods before receiving ALK inhibitor therapy; 14. Cohort 3: Signed informed consent form. Exclusion Criteria: 1. Cohort 1: Patients who have received treatment with Ensartinib after the project has started; 2. Cohort 1: Patients who have received Ensartinib treatment but have not completed the objective efficacy evaluation according to the follow-up cycle specified by the clinical physician; 3. Cohort 1: History of hypersensitivity reactions to active or inactive excipients of Ensartinib or to drugs with similar chemical structures or categories as Ensartinib; 4. Cohort 1: Patients who are participating in other clinical studies outside of this research; 5. Cohort 1: Other circumstances deemed unsuitable for enrollment by the researchers. 6. Cohort 2: Patients who have received Ensartinib treatment before the study started; 7. Cohort 2: Patients who have received other systemic treatments besides Ensartinib; 8. Cohort 2: Neoadjuvant treatment cycles less than 6 weeks or more than 12 weeks; 9. Cohort 2: Patients who have received Ensartinib monotherapy but have not completed the objective efficacy evaluation according to the follow-up cycle specified by the clinical physician; 10. Cohort 2: History of hypersensitivity reactions to active or inactive excipients of Ensartinib or to drugs with similar chemical structures or categories as Ensartinib; 11. Cohort 2: Patients who are participating in other clinical studies outside of this research; 12. Cohort 2: Other circumstances deemed unsuitable for enrollment by the researchers. 13. Cohort 3: Patients who have received neoadjuvant treatment containing Ensartinib but meet the enrollment criteria for Cohort 2; 14. Cohort 3: Patients who have received treatment containing Ensartinib but have not completed the objective efficacy evaluation according to the follow-up cycle specified by the clinical physician; 15. Cohort 3: History of hypersensitivity reactions to active or inactive excipients of Ensartinib or to drugs with similar chemical structures or categories as Ensartinib; 16. Cohort 3: Patients who are participating in other clinical studies outside of this research; 17. Cohort 3: Other circumstances deemed unsuitable for enrollment by the researchers.