# Elevated serum total immunoglobulin E is associated with an increased risk of lung cancer: a retrospective study

**Authors:** Dongmei Zhou, Jia Liu, Chu Zhang, Dan Kang, Jiayang Kang, Zihan Meng, Xiaonan Wang

PMC · DOI: 10.3389/fimmu.2025.1637803 · Frontiers in Immunology · 2025-07-21

## TL;DR

High levels of IgE in the blood are linked to a higher risk of lung cancer, suggesting IgE could be a diagnostic biomarker.

## Contribution

Identifies elevated serum total IgE as a novel risk factor and potential biomarker for lung cancer.

## Key findings

- Lung cancer patients had significantly higher serum IgE levels compared to healthy controls.
- Higher IgE levels were independently associated with increased lung cancer risk in smokers and elderly individuals.

## Abstract

This study investigated the correlation between serum total IgE levels and the risk of lung cancer using univariate and multivariate logistic regression analysis.

This cross-sectional retrospective cohort study included clinical and laboratory data from 675 lung cancer patients and 1,193 healthy controls.

The lung cancer patients showed significantly higher serum total IgE levels compared to healthy individuals, with 47.9% of patients having IgE levels >100 IU/ml (P < 0.01). Higher serum total IgE levels (>100 IU/ml) were significantly associated with increased risk of lung cancer (OR=1.534, 95% CI: 1.203-1.957; P < 0.001). Multivariate logistic regression analysis results showed that age ≥65 years (OR=4.775, 95% CI = 3.478–6.555; P <0.001), smoking history (OR=1.719, 95% CI = 1.198–2.466; P =0.003), and an elevated lymphocyte-to-monocyte ratio (LMR) (OR=0.777, 95% CI = 0.678–0.890; P <0.001) were independent risk factors for lung cancer development in subjects with serum total IgE levels >100 IU/ml. The higher the serum total IgE level, the higher the T stage, N stage, M stage and the later the tumor clinical stage (all P <0.001). Survival analysis did not show statistically significant differences in the median progression-free survival (PFS) (P>0.05) or overall survival (OS) (P>0.05) among advanced lung cancer patients with different IgE levels (high and low).

Lung cancer patients demonstrated elevated serum total IgE levels. Higher serum IgE levels were significantly associated with an increased risk of lung cancer. Therefore, serum total IgE level is a potential diagnostic biomarker for lung cancer. Moreover, IgE and its related allergic immune responses offer potential as innovative therapeutic targets in elderly lung cancer patients with an history of smoking and elevated monocyte counts.

## Linked entities

- **Proteins:** IGHE (immunoglobulin heavy constant epsilon)
- **Diseases:** lung cancer (MONDO:0005138)

## Full-text entities

- **Genes:** FCER1A (Fc epsilon receptor Ia) [NCBI Gene 2205] {aka FCE1A, FCERIA, FcERI}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, 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}, IDH1 (isocitrate dehydrogenase (NADP(+)) 1) [NCBI Gene 3417] {aka HEL-216, HEL-S-26, IDCD, IDH, IDP, IDPC}, Fcer1g (Fc receptor, IgE, high affinity I, gamma polypeptide) [NCBI Gene 14127] {aka CD23, FcR-gamma, FcR[g], FcRgamma, Fce1g, FcepsilonRI}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IGHE (immunoglobulin heavy constant epsilon) [NCBI Gene 3497] {aka IgE}, TENM1 (teneurin transmembrane protein 1) [NCBI Gene 10178] {aka ODZ1, ODZ3, TEN-M1, TEN1, TNM, TNM1}
- **Diseases:** LUSC (MESH:D002294), stage III NSCLC (MESH:D062706), hypertension (MESH:D006973), ovarian cancer (MESH:D010051), atopy (MESH:C564133), asthma (MESH:D001249), immunodeficiency (MESH:D007153), carcinogens (MESH:D011230), LC (MESH:D008175), atopic dermatitis (MESH:D003876), diabetes (MESH:D003920), eczema (MESH:D004485), LUAD (MESH:D000077192), IV (MESH:D006011), smoking (MESH:D015208), death (MESH:D003643), ES-SCLC (MESH:D055752), allergic (MESH:D004342), gliomas (MESH:D005910), non-small cell lung cancer (MESH:D002289), tumor node metastasis (MESH:D008207), metastasis (MESH:D009362), hematologic malignancies (MESH:D019337), coronary heart disease (MESH:D003327), cancers (MESH:D009369), immune-inflammation (MESH:D007249)
- **Chemicals:** alcohol (MESH:D000438)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

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## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC12318726/full.md

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Source: https://tomesphere.com/paper/PMC12318726