Lobectomy-First vs. Lymphadenectomy-First for Operable NSCLC (LOFTY)

NCT06577792 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 620

Last updated 2025-05-16

No results posted yet for this study

Summary

During the surgery for non-small cell lung cancer (NSCLC), lymphadenectomy or lobectomy are performed first, different surgeons have different choices. Oncology textbooks require dissecting distant lymph nodes (LNs) first and then dissecting nearby LNs. According to this requirement, thoracic surgeons should first perform lymphadenectomy and then lobectomy. Unfortunately, there is no high-level evidence to prove which surgical sequence is more beneficial to the long-term survival of NSCLC patients. In this multi-center randomized controlled trial (RCT), patients with stage I-II NSCLC were enrolled as the research object to determine which surgical sequence (lymphadenectomy-first vs. lobectomy-first) is better for the short-term and long-term outcomes in NSCLC patients.

Conditions

  • Non Small Cell Lung Cancer

Interventions

PROCEDURE

Lobectomy-First

During the surgical treatment for patients with NSCLC, thoracic surgeons should perform lobectomy first, and then perform lymphadenectomy next.

PROCEDURE

Lymphadenectomy-First

During the surgical treatment for patients with NSCLC, thoracic surgeons should perform lymphadenectomy first, and then perform lobectomy next.

Sponsors & Collaborators

  • Tianjin Medical University Cancer Institute and Hospital

    collaborator OTHER
  • RenJi Hospital

    collaborator OTHER
  • Sixth Affiliated Hospital, Sun Yat-sen University

    collaborator OTHER
  • First Affiliated Hospital of Jinan University

    collaborator OTHER
  • The First Affiliated Hospital with Nanjing Medical University

    collaborator OTHER
  • Shanghai Changzheng Hospital

    collaborator OTHER
  • Cancer Institute and Hospital, Chinese Academy of Medical Sciences

    collaborator OTHER
  • Suining Central Hospital

    collaborator OTHER
  • The Affiliated Hospital of Xuzhou Medical University

    collaborator OTHER
  • The General Hospital of Eastern Theater Command

    collaborator OTHER
  • Fujian Medical University Union Hospital

    collaborator OTHER
  • First Affiliated Hospital of Kunming Medical University

    collaborator OTHER
  • Fujian Provincial Hospital

    collaborator OTHER
  • Tianjin Chest Hospital

    collaborator OTHER
  • Sichuan Cancer Hospital and Research Institute

    collaborator OTHER
  • Tang-Du Hospital

    collaborator OTHER
  • Shandong Provincial Hospital

    collaborator OTHER_GOV
  • Gansu Provincial Hospital

    collaborator OTHER
  • Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

    collaborator OTHER
  • Wuhan TongJi Hospital

    collaborator OTHER
  • The Affiliated Hospital of Qingdao University

    collaborator OTHER
  • West China Hospital

    collaborator OTHER
  • Jiangsu Cancer Institute & Hospital

    collaborator OTHER
  • Dongguan People's Hospital

    collaborator OTHER_GOV
  • First People's Hospital of Foshan

    collaborator OTHER
  • Sun Yat-sen University

    lead OTHER

Principal Investigators

  • Hao-Xian Yang, M.D. · Sun Yat-sen University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-08-16
Primary Completion
2025-12-31
Completion
2030-12-31

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06577792 on ClinicalTrials.gov