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Low-Cost Single-Port LoCoSP Device for a Transcervical Approach in Minimally Invasive Transhiatal Esophagectomy
Published on: September 11, 2021
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Implementation of Minimally Invasive Esophagectomy From a Randomized Controlled Trial Setting to National Practice
Sheraz R Markar1, Melody Ni1, Suzanne S Gisbertz2
1Department Surgery and Cancer, Imperial College London, London, United Kingdom.
Summary
Minimally invasive esophagectomy (MIE) showed benefits in a trial but led to more complications nationally. This suggests MIE requires expert surgeons and high-volume centers for safe implementation.
Area of Science:
- Surgical Oncology
- Gastroenterology
- Clinical Trials
Background:
- The TIME trial evaluated minimally invasive esophagectomy (MIE) versus open esophagectomy.
- Assessing MIE's real-world effectiveness after national implementation is crucial.
Purpose of the Study:
- To examine the external validity of the TIME trial's findings on MIE.
- To compare MIE and open esophagectomy outcomes using national registry data.
Main Methods:
- Retrospective analysis of data from the TIME trial and the Dutch Upper GI Cancer Audit (DUCA).
- Multivariate analysis adjusted for patient, tumor, and surgical year factors.
- Inclusion of 115 patients from the TIME trial and 4,605 from the DUCA dataset.
Main Results:
- In the TIME trial, MIE reduced pulmonary complications and hospital stay.
- In the DUCA dataset, MIE was linked to more complications and reoperations but improved R0 margins and reduced 30-day mortality.
- Multivariate analysis of the DUCA data showed MIE increased total complications, pulmonary complications, and reoperations.
Conclusions:
- Nationally implemented MIE outside the TIME trial was associated with increased complications and reoperations.
- This may indicate challenges with non-expert surgeons performing MIE outside controlled, high-volume settings.
- MIE adoption requires careful consideration of surgeon expertise and center volume for optimal outcomes.

