AUTHOR=Chen Qin , Lin Kaihe , Zhang Baoteng , Jiang Youqin , Wu Suying , Lin Jiajun TITLE=CT morphological features and histogram parameters to predict micropapillary or solid components in stage IA lung adenocarcinoma JOURNAL=Frontiers in Oncology VOLUME=14 YEAR=2024 URL=https://www.frontiersin.org/journals/oncology/articles/10.3389/fonc.2024.1448333 DOI=10.3389/fonc.2024.1448333 ISSN=2234-943X ABSTRACT=Objectives

This study aimed to construct prediction models based on computerized tomography (CT) signs, histogram and morphology features for the diagnosis of micropapillary or solid (MIP/SOL) components of stage IA lung adenocarcinoma (LUAC) and to evaluate the models’ performance.

Methods

This clinical retrospective study included image data of 376 patients with stage IA LUAC based on postoperative pathology, admitted to Putian First Hospital from January 2019 to June 2023. According to the presence of MIP/SOL components in postoperative pathology, patients were divided into MIP/SOL+ and MIP/SOL- groups. Cases with tumors ≤ 3 cm and ≤ 2 cm were separately analyzed. Each subgroup of patients was then randomly divided into a training set and a test set in a ratio of 7:3. The training set was used to build the prediction model, and the test set was used for internal validation.

Results

For tumors ≤ 3 cm, ground-glass opacity (GGO) [odds ratio (OR) = 0.244; 95% confidence interval (CI): 0.103–0.569; p = 0.001], entropy (OR = 1.748; 95% CI: 1.213–2.577; p = 0.004), average CT value (OR = 1.002; 95% CI: 1.000–1.004; p = 0.002), and kurtosis (OR = 1.240; 95% CI: 1.023–1.513; p = 0.030) were independent predictors of MIP/SOL components of stage IA LUAC. The area under the ROC curve (AUC) of the nomogram prediction model for predicting MIP/SOL components was 0.816 (95% CI: 0.756–0.877) in the training set and 0.789 (95% CI: 0.689–0.889) in the test set. In contrast, for tumors ≤ 2 cm, kurtosis was no longer an independent predictor. The nomogram prediction model had an AUC of 0.811 (95% CI: 0.731–0.891) in the training set and 0.833 (95% CI: 0.733–0.932) in the test set.

Conclusion

For tumors ≤ 3 cm and ≤ 2 cm, GGO, average CT value, and entropy were the same independent influencing factors in predicting MIP/SOL components of stage IA LUAC. The nomogram prediction models have potential diagnostic value for identifying MIP/SOL components of early-stage LUAC.