Lobectomy-First Versus Lymphadenectomy-First Surgical Approach on Long-Term Survival in Operable Non-Small Cell Lung Cancer Patients: A Prospective, Multi-Center, Randomized Study

Status: Recruiting
Location: See all (26) locations...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 80
Healthy Volunteers: f
View:

• Age from 18 to 80 years old;

• The first clinical diagnosis before surgery was non-small cell lung cancer, including adenocarcinoma, squamous cell carcinoma, large cell carcinoma, and other unknown types;

• Clinical stage T1-2N0-1 (cI-II): Maximum diameter of tumor \<= 5 cm and short diameter of mediastinal lymph node \<= 1cm in thin layer computed tomography (CT);

• The patient's physical condition is able to tolerate lobectomy: (1) Goldman index 0-1; (2) Predicted forced expiratory volume in 1s (FEV1) \>= 40% and diffusing capacity of the lung for carbon monoxide (DLCO) \>= 40%; (3) Total bilirubin \<= 1.5 upper limit of normal; (4) Alanine aminotransferase (ALT)/Aspartate aminotransferase (AST) \<= 2.5 upper limit of normal; (5) Creatinine \<= 1.25 upper limit of normal and creatinine clearance rate (CCr) \>= 60 ml/min;

• Performance status of Eastern Cooperative Oncology Group (ECOG) = 0-1;

• All relevant examinations were completed within 28 days before the operation;

• Patients who understand this study and have signed an approved Informed Consent.

Locations
Other Locations
China
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
RECRUITING
Beijing
Sichuan Cancer Hospital and Research Institute
RECRUITING
Chengdu
West China Hospital
NOT_YET_RECRUITING
Chengdu
Dongguan People's Hospital
RECRUITING
Dongguan
First People's Hospital of Foshan
RECRUITING
Foshan
Fujian Medical University Union Hospital
RECRUITING
Fuzhou
Fujian Provincial Hospital
RECRUITING
Fuzhou
First Affiliated Hospital of Jinan University
RECRUITING
Guangzhou
Sixth Affiliated Hospital, Sun Yat-sen University
NOT_YET_RECRUITING
Guangzhou
Sun Yat-sen University Cancer Center
RECRUITING
Guangzhou
Shandong Provincial Hospital
NOT_YET_RECRUITING
Jinan
First Affiliated Hospital of Kunming Medical University
RECRUITING
Kunming
Gansu Provincial Hospital
RECRUITING
Lanzhou
Jiangsu Cancer Institute & Hospital
RECRUITING
Nanjing
The First Affiliated Hospital with Nanjing Medical University
NOT_YET_RECRUITING
Nanjing
The General Hospital of Eastern Theater Command
RECRUITING
Nanjing
The Affiliated Hospital of Qingdao University
NOT_YET_RECRUITING
Qingdao
RenJi Hospital
RECRUITING
Shanghai
Shanghai Changzheng Hospital
RECRUITING
Shanghai
Suining Central Hospital
RECRUITING
Suining
Tianjin Chest Hospital
NOT_YET_RECRUITING
Tianjin
Tianjin Medical University Cancer Institute and Hospital
RECRUITING
Tianjin
Wuhan TongJi Hospital
RECRUITING
Wuhan
Wuhan Union Hospital, China
NOT_YET_RECRUITING
Wuhan
Tang-Du Hospital
NOT_YET_RECRUITING
Xi'an
The Affiliated Hospital of Xuzhou Medical University
RECRUITING
Xuzhou
Contact Information
Primary
Hao-Xian Yang, M.D.
yanghx@sysucc.org.cn
+86-020-87343628
Backup
Mu-Zi Yang, M.D.
yangmz@sysucc.org.cn
+86-020-87341456
Time Frame
Start Date: 2023-08-16
Estimated Completion Date: 2030-12-31
Participants
Target number of participants: 620
Treatments
Other: Lobectomy-First group
Patients with operable NSCLC received lobectomy first then received lymphadenectomy for surgical treatment.
Other: Lymphadenectomy-First group
Patients with operable NSCLC received lymphadenectomy first then received lobectomy for surgical treatment.
Sponsors
Collaborators: Tianjin Medical University Cancer Institute and Hospital, Fujian Provincial Hospital, First Affiliated Hospital of Jinan University, The Affiliated Hospital of Xuzhou Medical University, RenJi Hospital, Suining Central Hospital, West China Hospital, First Affiliated Hospital of Kunming Medical University, Jiangsu Cancer Institute & Hospital, Shanghai Changzheng Hospital, The Affiliated Hospital of Qingdao University, First People's Hospital of Foshan, The First Affiliated Hospital with Nanjing Medical University, Gansu Provincial Hospital, Sichuan Cancer Hospital and Research Institute, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Tang-Du Hospital, Fujian Medical University Union Hospital, Sixth Affiliated Hospital, Sun Yat-sen University, The General Hospital of Eastern Theater Command, Wuhan TongJi Hospital, Tianjin Chest Hospital, Dongguan People's Hospital, Shandong Provincial Hospital, Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Leads: Sun Yat-sen University

This content was sourced from clinicaltrials.gov

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