4.1 Article

A prospective comparison of totally minimally invasive versus open Ivor Lewis esophagectomy

Journal

DISEASES OF THE ESOPHAGUS
Volume 26, Issue 3, Pages 263-271

Publisher

WILEY-BLACKWELL
DOI: 10.1111/j.1442-2050.2012.01356.x

Keywords

esophagectomy; esophagus; general surgery; minimally invasive; neoplasm; surgical procedure

Funding

  1. Clinical Research Training Fellowship from Cancer Research UK
  2. Medical Research Council (MRC)
  3. MRC [G1002565] Funding Source: UKRI
  4. Medical Research Council [G1002565] Funding Source: researchfish

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The majority of esophagectomies in Western parts of the world are performed by a transthoracic approach reflecting the prevalence of adenocarcinoma of the lower esophagus or esophagogastric junction. Minimally invasive esophagectomy (MIE) has been reported in a variety of formats, but there are no series that directly compare totally minimally invasive thoracolaparoscopic 2 stage esophagectomy (MIE-2) with open Ivor Lewis (IVL). A prospective single-center cohort study of patients undergoing elective MIE-2 or IVL between January 2005 and November 2010 was performed. Short-term clinicopathologic outcomes were recorded using validated systems. One hundred and six patients (median age 66, range 3685, 88 M:18 F) underwent two-stage esophagectomy (53 MIE-2 and 53 IVL). Patient demographics (age, sex, body mass index, American Society of Anesthesiologists grade, tumor characteristics, neoadjuvant chemotherapy, and TNM stage) were comparable between the two groups. Outcomes for MIE-2 and IVL were comparable for anastomotic leak rates (5 [9%] vs. 2 [4%], P= 0.241), resection margin clearance (R0) (43 [81%] vs. 38 [72%], P= 0.253), median lymph node yield (19 vs. 18, P= 0.584), and median length of stay (12 [range 791] vs. 12 [range 7101] days), respectively. Blood loss was significantly less for MIE-2 compared with IVL (median 300 [range 01250] mL vs. 400 [range 03000] mL, respectively, P= 0.021). MIE-2 in this series of selected patients supports its efficacy, when performed by an experienced minimally invasive surgical team. A well-designed multicenter trial addressing clinical effectiveness is now required.

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