Endoscopy Clinical Trials

Clinical trials related to Endoscopy Procedure

The Impact of Downstaging on Robotic Surgical Outcomes After Neoadjuvant Chemo-Immunotherapy in Non-Small Cell Lung Cancer

Status: Recruiting
Location: See all (10) locations...
Intervention Type: Procedure
Study Type: Observational
SUMMARY

The goal of this observational study is to learn whether tumor and nodal downstaging after neoadjuvant chemo-immunotherapy is associated with better surgical outcomes in patients with clinical stage IIB-III non-small cell lung cancer (NSCLC) undergoing robotic-assisted thoracic surgery. The main question it aims to answer is: Is downstaging after neoadjuvant chemo-immunotherapy associated with better surgical outcomes in patients with stage IIB-III NSCLC undergoing robotic-assisted surgery? Participants with resectable or potentially resectable stage IIB-III NSCLC who receive neoadjuvant chemo-immunotherapy as part of their routine clinical care and then undergo curative-intent robotic-assisted surgery will be prospectively enrolled from international centers. Clinical, operative, pathological, and postoperative outcome data will be collected, including R0 resection, the extent of resection, conversion to open surgery, postoperative complications, length of stay, readmission, and mortality.

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
View:

• Age ≥18 years

• Histologically confirmed NSCLC

• AJCC 9th clinical stage IIB-III, M0, deemed resectable or potentially resectable by the multidisciplinary tumour discussion (MDT)

• Planned neoadjuvant chemo-immunotherapy (PD-1/PD-L1 inhibitor + platinum doublet; additional neoadjuvant RT is allowed) with curative-intent surgery

• Received ≥1 cycle of chemo-IO (capture the intended 2-4 cycles)

• Baseline chest CT±PET-CT within 6 weeks before starting neoadjuvant therapy

• Restaging 2-6 weeks after last neoadjuvant dose with chest CT±PET-CT

• Curative-intent resection planned; surgery performed 2-10 weeks after last dose

• Performing systematic nodal dissection

• ECOG performance status 0-2.

• Complete 90-day postoperative follow-up

• Ability to provide informed consent

Locations
Other Locations
China
Fujian Medical University Union Hospital
RECRUITING
Fuzhou
Guangdong Provincial People's Hospital
RECRUITING
Guangzhou
Jiangsu Cancer Institute & Hospital
RECRUITING
Nanjing
The Affiliated Hospital of Qingdao University
RECRUITING
Qingdao
Shanghai Chest Hospital, Shanghai Jiao Tong University Medicine of School
RECRUITING
Shanghai
Shenzhen People's Hospital
RECRUITING
Shenzhen
Tianjin Medical University Cancer Institute & Hospital
RECRUITING
Tianjing
France
Hôpital Saint Joseph Marseille
RECRUITING
Marseille
University Hospital, Rouen
RECRUITING
Rouen
Italy
Azienda Ospedaliera di Cosenza
RECRUITING
Cosenza
Contact Information
Primary
Zhigang Li, MD, PhD
zhigang.li@shsmu.edu.cn
0086-021-22200000
Backup
Lin Huang, MD, PhD
dr.huang.lin@shsmu.edu.cn
0086-18116061178
Time Frame
Start Date: 2026-03-02
Estimated Completion Date: 2027-03-30
Participants
Target number of participants: 200
Treatments
ⅡB-Ⅲ NSCLC following Neo-Chemo-IO & RATS
Patients who are undergoing robotic-assisted thoracoscopic surgery for clinical stage ⅡB-Ⅲ non-small cell lung cancer following neoadjuvant chemoimmunotherapy
Sponsors
Leads: Shanghai Chest Hospital
Collaborators: Shenzhen People's Hospital, Guangdong Provincial People's Hospital, Jiangsu Cancer Institute & Hospital, Fujian Medical University Union Hospital, Hopital Saint Joseph Marseille, The Affiliated Hospital of Qingdao University, Azienda Ospedaliera Cosenza, University Hospital, Rouen, Tianjin Medical University Cancer Institute and Hospital

This content was sourced from clinicaltrials.gov