4.7 Article

The advanced lung cancer inflammation index is the optimal inflammatory biomarker of overall survival in patients with lung cancer

Journal

JOURNAL OF CACHEXIA SARCOPENIA AND MUSCLE
Volume 13, Issue 5, Pages 2504-2514

Publisher

WILEY
DOI: 10.1002/jcsm.13032

Keywords

Lung cancer; Prognosis; Inflammation indicators

Funding

  1. National Key Research and Development Program [2017YFC1309200]
  2. Beijing Municipal Science and Technology Commission [SCW2018-06]
  3. General Surgery Clinical Medical Center of Yunnan Province [ZX20190303]

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This study found that the ALI is the best indicator for predicting OS in lung cancer patients, regardless of gender, smoking status, or age less than 65 years. However, in non-small cell lung cancer and patients aged 65 years or older, the modified Glasgow prognostic score is superior to other indicators; in small cell lung cancer patients, the glucose-to-lymphocyte ratio has better prognostic ability.
Backgrounds Malnutrition and systemic inflammatory responses are associated with poor overall survival (OS) in lung cancer patients, but it remains unclear which biomarkers are better for predicting their prognosis. This study tried to determine the best one among the existing common nutrition/inflammation-based indicators of OS for patients with lung cancer. Materials and methods There were 16 nutrition or systemic inflammation-based indicators included in this study. The cut-off points for the indicators were calculated using maximally selected rank statistics. The OS was evaluated using the Kaplan-Meier estimator, and univariate and multivariate Cox proportional hazard models were used to determine the relationship between the indicators and OS. A time-dependent receiver operating characteristic curves (time-ROC) and C-index were calculated to assess the predictive ability of the different indicators. Results There were 1772 patients with lung cancer included in this study. In univariate analysis, all 16 indicators were significantly associated with OS of the patients (all P < 0.001). Except for platelet-to-lymphocyte ratio, all other indicators were independent predictors of OS in multivariate analysis (all P < 0.05). Low advanced lung cancer inflammation index (ALI) was associated with higher mortality risk of lung cancer [hazard ratio, 1.30; 95% confidence interval (CI), 1.13-1.49]. The results of the time-AUC and C-index analyses indicated that the ALI (C-index: 0.611) had the best predictive ability on the OS in patients with lung cancer. In different sub-groups, the ALI was the best indicator for predicting the OS of lung cancer patients regardless of sex (C-index, 0.609 for men and 0.613 for women) or smoking status (C-index, 0.629 for non-smoker and 0.601 for smoker) and in patients aged <65 years (C-index, 0.613). However, the modified Glasgow prognostic score was superior to the other indicators in non-small cell lung cancer patients (C-index, 0.639) or patients aged >= 65 years (C-index, 0.610), and the glucose-to-lymphocyte ratio performed better prognostic ability in patients with small cell lung cancer (C-index, 0.601). Conclusions The prognostic ability of the ALI is superior to the other inflammation/nutrition-based indicators for all patients with lung cancer.

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