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Updated: Nov 29, 2025

Subcostal Specimen Removal in Completely Portal Robotic Lobectomy
Published on: April 19, 2024
Mortality for Robotic- vs Video-Assisted Lobectomy-Treated Stage I Non-Small Cell Lung Cancer Patients.
Yong Cui1, Eric L Grogan2, Stephen A Deppen2
1Division of Epidemiology, Department of Medicine, Vanderbilt Epidemiology Center, Vanderbilt-Ingram Cancer Center, Vanderbilt University School of Medicine, Nashville, TN, USA.
Robotic-assisted thoracoscopic lobectomy (RATS-L) for small non-small cell lung cancer (NSCLC) showed higher long-term mortality than video-assisted thoracoscopic lobectomy (VATS-L). This risk was evident after one year post-surgery, particularly for tumors 20mm or less.
Area of Science:
- Thoracic Surgery
- Surgical Oncology
- Minimally Invasive Procedures
Background:
- US FDA safety concerns regarding robotic surgery necessitate comparative outcome analyses.
- Stage I non-small cell lung cancer (NSCLC) is frequently treated with lobectomy.
- Robotic-assisted thoracoscopic surgical lobectomy (RATS-L) and video-assisted thoracoscopic surgical lobectomy (VATS-L) are common minimally invasive approaches.
Purpose of the Study:
- To compare short- and long-term mortality between RATS-L and VATS-L for stage I NSCLC.
- To evaluate the impact of tumor size on mortality differences between RATS-L and VATS-L.
- To provide evidence for clinical decision-making in NSCLC surgical treatment.
Main Methods:
- Analysis of 18,908 stage I NSCLC patients from the National Cancer Database (2010-2014).
- Comparison of RATS-L versus VATS-L using Cox proportional hazards models.
- Propensity score-matched and unmatched analyses to estimate mortality hazard ratios (HRs).
Main Results:
- RATS-L showed higher 90-day mortality than VATS-L when conversion to open thoracotomy occurred (6.6% vs 3.8%).
- For tumors ≤20mm, RATS-L was associated with increased long-term mortality (HRs ranging from 1.17 to 1.36) in intention-to-treat analyses.
- No significant mortality difference was observed for tumors >20mm or in patients without conversion to open surgery.
Conclusions:
- Patients with small (≤20mm) stage I NSCLC treated with RATS-L face a statistically significant higher long-term mortality risk compared to VATS-L.
- The increased mortality risk with RATS-L for small tumors persists beyond the first year post-surgery.
- Findings highlight the importance of considering surgical approach based on tumor characteristics and potential conversion risks.
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