Sleeve Lobectomy for Lung Cancer in Minimally Invasive Surgical Techniques

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorSecond Affiliated Hospital, School of Medicine, Zhejiang University

About this trial

The goal of this multicenter observational study is to evaluate the long-term survival and perioperative outcomes of sleeve lobectomy in robotic-assisted thoracic surgery (RATS) for patients with central lung cancer when compared with video-assisted thoracic surgery (VATS) approach, both of which have been already applied to these patients in minimally invasive surgical techniques as part of their regular medical care recently. The main question it aims to answer is:

Are RATS sleeve lobectomy associated with similar or even better long-term survival and perioperative outcomes for patients with central lung cancer when compared with the VATS approach?

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥ 18 years;

Clinically suspected lung cancer with a high likelihood of undergoing sleeve lobectomy;

Postoperative histopathological diagnosis confirms non-small cell lung cancer (NSCLC);

No history of malignancy within the past 5 years;

Disqualifiers

Unable to undergo surgical resection due to surgical contraindications;

Postoperative pathology does not confirm non-small cell lung cancer (NSCLC), including but not limited to benign lesions, small cell lung cancer, metastatic tumors, or an insufficient or indeterminate histopathology report;

History of malignancy within the past 5 years;

Unable to obtain follow-up data;

Trial population

This study will retrospectively enroll 450 consecutive patients with stage IA\~IIIB non-small cell lung cancer performed sleeve lobectomy in minimally invasive surgical techniques (RATS or VATS) from January 2015 to September 2024 in all three related centers. Baseline clinical information, surgery-related data, short-term postoperative outcomes, and long-term survival data (3-year OS and RFS) will be collected and analyzed using the propensity score matching method.

Trial design

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

  • RATS Group

    Procedure/Surgery

    The participants with centrally located lung cancer in this group were performed sleeve lobectomy in robotic-assisted thoracic surgery (RATS) approach, which has been already applied to these patients in minimally invasive surgical techniques as part of their regular medical care recently.

  • VATS group

    Procedure/Surgery

    The participants with centrally located lung cancer in this group were performed sleeve lobectomy in video-assisted thoracic surgery (VATS) approach.

Treatment groups

450 Participants
are divided into 1 treatment group
Group A: Lung cancer cohort of sleeve lobectomy in minimally invasive surgical approaches2 interventions

Trial outcomes

Primary outcomes

1

3-year RFS

In this study, the investigators will focus on the 3-year recurrence-free survival (RFS) of the participants between the two groups (RATS vs. VATS) for the comparison of the long-term oncologic outcomes, as the primary outcome.

Time frame
3 years

Secondary outcomes

1

3-year OS

The investigators will also focus on the 3-year overall survival (OS) of the participants between the two groups (RATS vs. VATS) for the comparison of the long-term oncologic outcomes, as the secondary outcome.

Time frame
3 years

Other outcomes

1

Intraoperative blood loss

The intraoperative blood loss will be investigated between RATS versus VATS sleeve lobectomy as one of the perioperative outcomes, measured in milliliter (mL).

Time frame
up to 90 days
2

Operative time

The operative time will be investigated between RATS versus VATS sleeve lobectomy as one of the perioperative outcomes, measured in minute (min).

Time frame
up to 90 days
3

Length of hospital stay

The length of hospital stay will be investigated between RATS versus VATS sleeve lobectomy as one of the perioperative outcomes, measured in day.

Time frame
up to 90 days
4

Postoperative drainage

The postoperative drainage will be investigated between RATS versus VATS sleeve lobectomy as one of the perioperative outcomes, measured in milliliter (mL).

Time frame
up to 90 days

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Second Affiliated Hospital, School of Medicine, Zhejiang University

Lead sponsor

Shanghai Chest Hospital of Shanghai Jiao Tong University

Collaborator

Sir Run Run Shaw Hospital

Collaborator