# Impact of Thoracic Duct Resection on Postoperative Body Composition Trajectory After Oesophagectomy: A Prospective Cohort Study

**Authors:** Tae Hee Hong, Young Ho Yang, Ha Eun Kim, Byung Jo Park, Chang Young Lee, Jin Gu Lee, Dae Joon Kim

PMC · DOI: 10.1002/jcsm.70209 · 2026-02-10

## TL;DR

This study finds that thoracic duct resection during oesophagectomy leads to a temporary but significant loss of muscle mass in the first three months post-surgery.

## Contribution

The study is the largest to date examining longitudinal body composition changes after thoracic duct resection using serial bioelectrical impedance analysis.

## Key findings

- Thoracic duct resection was associated with a more pronounced decline in skeletal muscle mass indices during the first three months post-surgery.
- Muscle mass recovery began around three months post-surgery, with no significant differences in sarcopenia-related indices by 12 months.
- The observed muscle loss appeared to be procedure-related rather than tumor-related, as similar patterns were seen in early-stage patients.

## Abstract

Thoracic duct resection (TDR) is frequently performed during radical oesophagectomy to improve locoregional control in oesophageal squamous cell carcinoma (ESCC). However, its impact on postoperative body composition—particularly skeletal muscle mass—remains unclear. This study aimed to evaluate the extent and temporal pattern of postoperative changes in adiposity‐ and sarcopenia‐related indices following TDR.

In this prospective cohort study, 347 patients with ESCC who underwent curative oesophagectomy between May 2018 and June 2022 were included. Patients were classified into a TDR group (n = 288) and a thoracic duct preservation group (n = 59). Body composition was assessed using bioelectrical impedance analysis (BIA) at six time points: preoperatively and 1, 2, 3, 6 and 12 months postoperatively, yielding 1925 measurements. Metrics analysed included body mass index (BMI), fat mass index (FMI), skeletal muscle mass index (SMI) and fat‐free mass index (FFMI). Sensitivity analysis was performed using 1:1 propensity score matching (PSM), based on key clinical variables.

Median age was 64 years, and ~90% of patients were male in both groups. Baseline operative variables were comparable between groups, including operative time (485 vs. 478 min), total lymph nodes (66 vs. 63) and complication rates (30% vs. 32%). BMI and FMI declined gradually over 12 months with no significant between‐group differences (BMI at 12 months: TDR vs. preservation, 21.0 vs. 20.6 kg/m2; p = 0.809). In contrast, SMI and FFMI showed significant early postoperative declines, with more pronounced reductions in the TDR group during the first 3 months (SMI: −11.2% vs. −8.1%, p = 0.036). These early differences attenuated after PSM but remained directionally consistent. Recovery of muscle mass began around postoperative month 3, and by 12 months, sarcopenia‐related indices were comparable between groups (SMI: p = 0.343; FFMI: p = 0.733). Subgroup analysis in patients with clinical stage I disease revealed similar patterns, suggesting that the observed muscle loss may reflect procedure‐related effects, independent of tumour burden. Exploratory nutritional markers—including albumin, lymphocyte count and cholesterol—showed no significant intergroup differences at any interval.

This is the largest study to date to assess longitudinal body composition changes after TDR using serial BIA. TDR was associated with a greater decline in sarcopenia‐related indices, particularly within the first 3 months. These effects were transient, reversible and reproducible in early‐stage patients. Our findings support the oncologic role of TDR while underscoring the importance of early nutritional and rehabilitative care.

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** complication (MESH:D008107), adiposity (MESH:D018205), ESCC (MESH:D004938), oesophageal squamous cell carcinoma (MESH:D000077277), sarcopenia (MESH:D055948), tumour (MESH:D009369), muscle loss (MESH:D009135)
- **Chemicals:** cholesterol (MESH:D002784)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12891974/full.md

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Source: https://tomesphere.com/paper/PMC12891974