# Minimally invasive or open esophagectomy for esophageal squamous cell carcinoma: a comprehensive systematic review of surgical and survival outcomes

**Authors:** Anas B. Barnawi, Waseem M. Hajjar, Adel D. Almaymuni, Ammar Alzahim, Osama Thamer Al-Ahmari, Basim Alshahrani, Abdulaziz Aljanoubi, Layan Rafat Bukhari, Muhanad Sultan Alsharari, Meshari Abdulrahman Al-Sahli, Abdulmalik Abdulelah Bin Kassim, Aldana Alodayani

PMC · DOI: 10.3389/fsurg.2026.1734948 · Frontiers in Surgery · 2026-02-17

## TL;DR

This study compares minimally invasive and open esophagectomy for esophageal cancer, finding similar cancer outcomes but better recovery with the minimally invasive approach.

## Contribution

The paper provides the first comprehensive systematic review comparing surgical and survival outcomes of MIE and OE specifically for ESCC.

## Key findings

- MIE and OE showed comparable oncologic outcomes including R0 resection rates and lymph node yield.
- MIE had reduced blood loss, shorter hospital stays, and fewer pulmonary complications compared to OE.
- Five out of nine studies found no significant differences in overall or disease-free survival between the two approaches.

## Abstract

Esophageal squamous cell carcinoma (ESCC) remains a common malignancy with high mortality. Minimally invasive esophagectomy (MIE) was developed to reduce the morbidity of conventional open esophagectomy (OE), but comparative evidence specifically addressing oncologic adequacy and postoperative recovery in ESCC is limited. This systematic review synthesizes comparative data on MIE vs. OE in ESCC.

We conducted a PRISMA-compliant systematic review registered on PROSPERO (CRD420251158559). PubMed/MEDLINE, Web of Science, and the Cochrane Library were searched for studies published between January 2010 and May 2024. Nine comparative studies (n = 5,342; 2,968 MIE, 2,374 OE) met inclusion criteria. Methodological quality was assessed using the Newcastle–Ottawa Scale. Prespecified endpoints included overall survival (OS), disease-free survival (DFS), lymph node yield, R0 resection rate, perioperative complications, intraoperative blood loss, and lengths of ICU and hospital stay.

Aggregate data indicate oncologic equivalence between MIE and OE: R0 resection rates were uniformly high (≥92%), and lymph node yields were comparable. Five out of nine studies (55.6%) reported no statistically significant differences in overall survival (OS) or disease-free survival (DFS) between MIE and OE. However, selected analyses favored MIE (e.g., 3-year OS HR 0.54, 95% CI 0.43–0.68). Perioperatively, MIE demonstrated consistent advantages, including reduced intraoperative blood loss, shorter hospital length of stay, and lower rates of pulmonary complications—particularly pneumonia—each of which was reported in seven of the nine included studies (77.8%). Anastomotic leak rates were similar; reports of recurrent laryngeal nerve injury were heterogeneous.

In ESCC, MIE achieves oncologic outcomes comparable to OE while conferring reduced pulmonary morbidity, lower blood loss, and accelerated postoperative recovery, supporting its consideration as a standard surgical approach.

https://www.crd.york.ac.uk/PROSPERO/view/CRD420251158559, PROSPERO CRD420251158559.

## Linked entities

- **Diseases:** esophageal squamous cell carcinoma (MONDO:0005580)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** Esophagus (MESH:D004938), MIE (MESH:D009361), OE (MESH:D005597), deaths (MESH:D003643), leak (MESH:D019559), anastomotic leak (MESH:D057868), bleeding (MESH:D006470), Pneumonia (MESH:D011014), RLN palsy (MESH:D010243), fatigue (MESH:D005221), squamous cell carcinoma (MESH:D002294), complication (MESH:D008107), pulmonary infections (MESH:D012141), trauma (MESH:D014947), respiratory complication (MESH:D012140), Recurrent laryngeal nerve injury (MESH:D061226), pain (MESH:D010146), Cancer (MESH:D009369), postoperative pain (MESH:D010149), adenocarcinoma (MESH:D000230), Pulmonary complications (MESH:D008171), morbidities (OMIM:614963), Blood loss (MESH:D016063), ESCC (MESH:D000077277)
- **Chemicals:** MIE (-), Ivor (MESH:C118296)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12954734/full.md

## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC12954734/full.md

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Source: https://tomesphere.com/paper/PMC12954734