RecruitingNot ApplicableNCT06577792

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

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


Sponsor

Sun Yat-sen University

Enrollment

620 participants

Start Date

Aug 16, 2023

Study Type

INTERVENTIONAL

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

Min Age: 18 YearsMax Age: 80 Years

Inclusion Criteria7

  • 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.

Exclusion Criteria9

  • Patients who have undergone anti-tumor therapy (radiotherapy, chemotherapy, targeted therapy, immunotherapy) before surgery;
  • Patients with previous medical history of other malignant tumors or combined with second primary cancer at the time of enrollment;
  • Patients who meet all of the following criteria are eligible for sublobar resection (segment/wedge resection): (1) Ground glass opacity (GGO) with a solid component \<= 50%; (2) The largest diameter of nodule is \<= 2 cm; (3) The nodule is located in the outer third of the lung field;
  • Patients with preoperative diagnosis of pure GGO;
  • Patients with previous medical history of unilateral thoracotomy;
  • Women who are pregnant or breastfeeding;
  • Patients with active bacterial or fungal infection that is difficult to control;
  • Patients with serious psychosis;
  • Patients with a history of severe heart disease, heart failure, myocardial infarction or angina pectoris in the past 6 months.

Interventions

PROCEDURELobectomy-First

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

PROCEDURELymphadenectomy-First

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


Locations(26)

Cancer Institute and Hospital, Chinese Academy of Medical Sciences

Beijing, Beijing Municipality, China

Fujian Medical University Union Hospital

Fuzhou, Fujian, China

Fujian Provincial Hospital

Fuzhou, Fujian, China

Gansu Provincial Hospital

Lanzhou, Gansu, China

Dongguan People's Hospital

Dongguan, Guangdong, China

First People's Hospital of Foshan

Foshan, Guangdong, China

Sun Yat-sen University Cancer Center

Guangzhou, Guangdong, China

First Affiliated Hospital of Jinan University

Guangzhou, Guangdong, China

Sixth Affiliated Hospital, Sun Yat-sen University

Guangzhou, Guangdong, China

Wuhan TongJi Hospital

Wuhan, Hubei, China

Wuhan Union Hospital, China

Wuhan, Hubei, China

Jiangsu Cancer Institute & Hospital

Nanjing, Jiangsu, China

The General Hospital of Eastern Theater Command

Nanjing, Jiangsu, China

The First Affiliated Hospital with Nanjing Medical University

Nanjing, Jiangsu, China

The Affiliated Hospital of Xuzhou Medical University

Xuzhou, Jiangsu, China

Tang-Du Hospital

Xi'an, Shaanxi, China

Shandong Provincial Hospital

Jinan, Shandong, China

The Affiliated Hospital of Qingdao University

Qingdao, Shandong, China

RenJi Hospital

Shanghai, Shanghai Municipality, China

Shanghai Changzheng Hospital

Shanghai, Shanghai Municipality, China

Sichuan Cancer Hospital and Research Institute

Chengdu, Sichuan, China

West China Hospital

Chengdu, Sichuan, China

Suining Central Hospital

Suining, Sichuan, China

Tianjin Medical University Cancer Institute and Hospital

Tianjin, Tianjin Municipality, China

Tianjin Chest Hospital

Tianjin, Tianjin Municipality, China

First Affiliated Hospital of Kunming Medical University

Kunming, Yunnan, China

View Full Details on ClinicalTrials.gov

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NCT06577792