Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ENROLLING_BY_INVITATION
500 participants
OBSERVATIONAL
2024-11-01
2025-10-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Patients who have undergone radical lung cancer surgery.
* Patients who have received neoadjuvant treatment before radical lung cancer surgery, including chemotherapy, targeted therapy, or immunotherapy both alone or combined.
Exclusion Criteria
* Patients with incomplete key baseline and treatment information,including clinical stage, pathological type, neoadjuvant treatment, pathological response, imaging response after neoadjuvant.
* Patients included in anti-tumor drug intervention or unblinded clinical trials, in which the treatment being administered is unknown.
* Prior surgery, radiotherapy or systemic therapy for NSCLC, including radiofrequency ablation, etc.
ALL
No
Sponsors
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Shanghai Chest Hospital
OTHER
Responsible Party
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Hua Zhong
professor
Principal Investigators
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Zhong Dr., MD
Role: STUDY_CHAIR
Shanghai Chest Hospital
Locations
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Zhong Hua
Shanghai, Shanghai Municipality, China
Countries
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Other Identifiers
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IS24118
Identifier Type: -
Identifier Source: org_study_id
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