Safety, Efficacy, and Survival Outcomes of Neoadjuvant/Induction Immunotherapy in Surgical and Radiotherapeutic Management of Non-Small Cell Lung Cancer

RecruitingOBSERVATIONAL
Enrollment

500

Participants

Timeline

Start Date

December 1, 2024

Primary Completion Date

March 31, 2026

Study Completion Date

March 31, 2028

Conditions
Lung Cancer (NSCLC)Neoadjuvant ImmunotherapyRadiotherapyLung Surgery
Interventions
DRUG

neoadjuvant immunotherapy

"Patients in the cohort received neoadjuvant immune checkpoint inhibitors (ICIs), including PD-1/PD-L1 inhibitors, as part of routine clinical care. The specific regimens included monotherapy or combination with chemotherapy. The agents used may include nivolumab, camrelizumab, sintilimab, atezolizumab, or others.~This is a retrospective observational study. All interventions (neoadjuvant immunotherapy ± chemotherapy, surgery, or other treatments) were determined by treating physicians as part of standard care. The study aims to evaluate perioperative and survival outcomes across different treatment paths in real-world clinical settings."

Trial Locations (4)

100142

RECRUITING

Peking University Cancer Hospital & Institute, Beijing

Unknown

RECRUITING

Peking University Third Hospital, Beijing

RECRUITING

Inner Mongolia Hospital of Peking University Cancer Hospital, Hohhot

RECRUITING

The Third Affliated Hospital of Kunming Medical University, Kunming

All Listed Sponsors
lead

Peking University Cancer Hospital & Institute

OTHER