Actively Recruiting

Age: 18Years +
All Genders
NCT07135856

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

Shanghai Chest Hospital

Shanghai, Shanghai Municipality, China, 200000

Actively Recruiting

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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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