Actively Recruiting
Sleeve Lobectomy Following Neoadjuvant Therapy in NSCLC
Led by Shanghai Chest Hospital · Updated on 2025-12-31
400
Participants Needed
1
Research Sites
65 weeks
Total Duration
On this page
Sponsors
S
Shanghai Chest Hospital
Lead Sponsor
S
Sir Run Run Shaw Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this observational, retrospective, multicenter cohort study is to evaluate the surgical and oncologic outcomes of sleeve lobectomy performed via minimally invasive (RATS/VATS) or open thoracotomy approaches in patients with non-small cell lung cancer (NSCLC) who have undergone neoadjuvant therapy, including chemotherapy, immunotherapy, or combination regimens. The main questions this study aims to answer are: * Does minimally invasive sleeve lobectomy result in comparable or improved perioperative and postoperative outcomes compared to open thoracotomy following neoadjuvant treatment in NSCLC? * Does surgical approach influence oncologic endpoints such as margin status, lymph node dissection, recurrence-free survival, and overall survival? This research addresses a critical gap in the thoracic oncology field by evaluating the safety, complexity, and efficacy of advanced surgical techniques in the context of evolving multimodal therapy paradigm. Findings may inform clinical decision-making and optimize patient selection in an era of increasing use of neoadjuvant strategies for resectable NSCLC.
CONDITIONS
Official Title
Sleeve Lobectomy Following Neoadjuvant Therapy in NSCLC
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 2 18 years
- Histologically confirmed NSCLC
- Undergoing sleeve lobectomy with curative intent
- Received neoadjuvant therapy (chemotherapy, immunotherapy, targeted therapy, etc.)
- Surgical approach is minimally invasive (VATS or RATS) or open thoracotomy
- Complete perioperative and follow-up data available (at least 12 months or until death)
- Signed informed consent
You will not qualify if you...
- Sublobar resections like segmentectomy or pneumonectomy
- No neoadjuvant therapy received
- Surgery done only for diagnostic purposes
- Incomplete medical records or lost to follow-up
- Metastatic (stage IV) disease at time of surgery
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Shanghai Chest Hospital
Shanghai, Shanghai Municipality, China, 200000
Actively Recruiting
Research Team
X
Xinghua Cheng, M.D., Ph.D.
CONTACT
Z
Zhebing Lin, M.D.
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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