# The Role of Omega-3 Polyunsaturated Fatty Acid Supplementation in Postoperative Recovery of Colorectal Cancer: Systematic Review and Meta-Analysis

**Authors:** Huzhong Li, Zhenze Xu, Yamin Chen, Jianming Guo, Qihe Wang, Dong Liang, Pengfeng Qu, Taotao Deng, Yuan Yuan, Jiao Xu, Haiqin Fang, Ziyuan Wang

PMC · DOI: 10.3390/nu18010173 · Nutrients · 2026-01-05

## TL;DR

This study finds that omega-3 fatty acid supplements help colorectal cancer patients recover better after surgery by reducing inflammation and improving immune function and hospital stays.

## Contribution

The study identifies an optimal dosage range of omega-3 PUFAs for Chinese CRC patients, offering evidence for FSMP standards and clinical protocols.

## Key findings

- Omega-3 PUFA supplementation significantly improves nutritional markers and immune parameters in CRC patients.
- Supplements reduce inflammation and postoperative complications like hospitalization duration and infections.
- A dose range of 0.16–0.30 g/kg/day is suggested as optimal for Chinese CRC patients.

## Abstract

Background: China is currently developing standards for Food for Special Medical Purposes (FSMP) targeting for oncology patients. However, substantial challenges remain in defining optimal fortification levels of omega-3 polyunsaturated fatty acids (ω-3 PUFAs). Accumulating evidence suggests that ω-3 PUFA intake improves postoperative prognosis by modulating oncological parameters in colorectal cancer (CRC) patients. This meta-analysis aimed to evaluate the therapeutic efficacy of ω-3 PUFA supplementation in enhancing postoperative safety and recovery stability following CRC surgery, to address critical gaps in nutritional interventions for optimizing clinical outcomes. These findings are expected to FSMP standard development, clinical nutrition protocols and product innovation. Methods: A systematic literature search was conducted, in accordance with PRISMA guidelines, across major databases until June 16, 2025. Data were analyzed using RevMan v5.4 (Cochrane Collaboration). Results: Thirty-four randomized controlled trials (RCTs) (n = 2889) were included. Compared to controls, the ω-3 PUFAs group showed significantly increased levels of nutritional markers: total protein (p < 0.00001), albumin (p = 0.001); immunological parameters: CD3+/CD4+/CD8+ T-cells, CD4+/CD8+ ratio (all p < 0.0001); Karnofsky Performance Status (KPS) scores (p = 0.04); and serum ω-3 PUFA concentrations (p = 0.0004). Significant reductions were observed in inflammatory markers, such as procalcitonin, C-reactive protein (CRP), interleukin-6 (IL-6), tumor necrosis factor-α (TNF-α) (p = 0.004 to < 0.00001); and clinical outcomes, such as hospitalization duration (p < 0.00001), infectious complications (p < 0.00001), anastomotic leakage (p = 0.0005), surgical site infections (p = 0.03). No significant intergroup differences were detected for white blood cells, transcription factor activity, mortality, or crypt cell proliferation indices (p = 0.06–0.55). Conclusions: Overall, ω-3 PUFA supplementation significantly attenuates postoperative inflammation, enhances immune function, shortens hospitalization, and improves the quality of life in CRC patients, though without mortality benefit. Notably, post hoc dose–response analysis identified a supplementation range of 0.16–0.30 g/kg/day as a potentially optimal supplementation range for Chinese CRC populations, providing foundational evidence for clinical practice and FSMP standardization.

## Linked entities

- **Proteins:** cd.3 (Cd.3 conserved hypothetical protein), CD4 (CD4 molecule), CD8A (CD8 subunit alpha), IL6 (interleukin 6)
- **Chemicals:** omega-3 PUFA (PubChem CID 56842239)
- **Diseases:** colorectal cancer (MONDO:0005575)

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}
- **Diseases:** inflammation (MESH:D007249), infections (MESH:D007239), anastomotic leakage (MESH:D057868), infectious complications (MESH:D003141), CRC (MESH:D015179)
- **Chemicals:** Omega-3 Polyunsaturated Fatty Acid (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

18 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12787802/full.md

## References

72 references — full list in the complete paper: https://tomesphere.com/paper/PMC12787802/full.md

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Source: https://tomesphere.com/paper/PMC12787802