Prediction of differentiation levels in lung adenocarcinoma using peripheral blood inflammatory cytokines and tumor markers

Y Yang Li J Jiahuan Wu M Meiling Long T Tingting Zeng D Depeng Jiang

Abstract

Objective Lung Adenocarcinoma (LUAD) has highly aggressive and lethal, and its degree of differentiation significantly influences prognosis and treatment strategies, yet accurate prediction remains challenging. To assess the predictive value of combining peripheral blood inflammatory markers, such as the aggregate index of systemic inflammation (AISI), with tumor markers, including Carcinoembryonic Antigen (CEA) and Cytokeratin 19 fragment antigen 21−1(CYFRA21−1), etc, for determining LUAD differentiation levels. Methods This retrospective study included 203 LUAD patients treated at Chongqing Medical University’s Second Affiliated Hospital, categorized by low and high differentiation. Demographic, clinical, and laboratory data including peripheral blood inflammatory and tumor markers were analyzed. A multivariate logistic regression model evaluated these markers’ predictive accuracy. Results AISI (OR = 1.64, 95% CI = 1.08–2.58, p  = 0.024), CEA (OR = 1.02, 95% CI = 1.00–1.04, p  = 0.0497), ferritin (OR = 1.01, 95% CI = 1.00–1.01, p  = 0.010), and Progastrin Releasing Peptide (ProGRP) (OR = 1.03, 95% CI = 1.00–1.07, p  = 0.047) were risk factors of low differentiation LUAD. The model achieved an Area Under Curve(AUC) of 0.795 (95%CI: 0.726–0.864) for distinguishing low from high differentiation, with decision curve analysis confirming clinical utility. Conclusion This model, combining inflammatory and tumor markers, effectively predicts LUAD differentiation, aiding personalized treatment planning, enhancing therapeutic outcomes, and supporting early LUAD detection.

Article Details

Journal PLoS ONE
Volume / Issue Vol. 21, Issue 1
Published January 08, 2026
Pages e0339414
ISSN 1932-6203
Publisher Public Library of Science

Journal Info

PLoS ONE

Public Library of Science

ISSN: 1932-6203 Open Access Health Sciences

Authors (5)

Y

Yang Li

J

Jiahuan Wu

M

Meiling Long

T

Tingting Zeng

D

Depeng Jiang