Lung Adenocarcinoma Clinical Trial
Official title:
Comparison of Video-assisted Thoracoscopic Segmentectomy Versus Lobectomy for Lung Adenocarcinoma in Situ and With Microinvasion
This is a Prospective, open-label, parallel, multi-center, Phase III randomized trial to evaluate the efficacy and safety of video-assisted thoracoscopic segmentectomy versus Lobectomy in treating patients with Lung adenocarcinoma in situ or with microinvasion.
Lobectomy has long been considered the standard procedure for early-stage lung cancer, and
minimally invasive techniques have been demonstrated to be associated with superior outcomes
compared with lobectomy by thoracotomy. the us of segmentectomy is under investigation for
selected patients with small tumors, and the use of minimally invasive strategies is
applicable as well.
This nationwide, multicenter, prospective, randomized open phase III study of cVATS
(complete Video-assisted Thoracoscopic Surgery) segmentectomy versus Lobectomy for stage IA
non-small cell lung cancer (NSCLC) patients with Lung adenocarcinoma in situ or with
microinvasion, is aiming to evaluate the relapse free survival and 5 year overall survival
(OS) rate of two types of surgery. Patients are randomized to 1 of 2 treatment arms.
- Arm I: Patients undergo cVATS lobectomy.
- Arm II: Patients undergo cVATS segmentectomy.
Patients will be followed up every 3 months within the first year, and annually for 5 years
postoperatively.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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