Predicting pathological response to neoadjuvant or conversion chemoimmunotherapy in stage IB–III non‐small cell lung cancer patients using radiomic features

Author:

Yang Nong12,Yue Hai‐Lin1,Zhang Bai‐Hua3,Chen Juan4,Chu Qian5,Wang Jian‐Xin2,Yu Xiao‐Ping6,Jian Lian6,Bin Ya‐Wen7,Liu Si‐Ye6,Liu Jin2,Zeng Liang1,Yang Hai‐Yan1,Zhou Chun‐Hua1,Jiang Wen‐Juan1,Liu Li1,Zhang Yong‐Chang1ORCID,Xiong Yi1,Wang Zhan1

Affiliation:

1. Hunan Provincial Key Lab on Bioinformatics, School of Computer Science and Engineering Central South University Changsha China

2. Lung Cancer and Gastrointestinal Unit, Department of Medical Oncology, Hunan Cancer Hospital and the Affiliated Cancer Hospital of Xiangya School of Medicine Central South University Changsha China

3. Department of Thoracic Surgery Hunan Cancer Hospital Changsha China

4. Department of Pharmacy, Xiangya Hospital Central South University Changsha China

5. Department of Oncology, Tongji Hospital, Tongji Medical College Huazhong University of Science and Technology Wuhan China

6. Department of Diagnostic Radiology, Hunan Cancer Hospital and the Affiliated Cancer Hospital of Xiangya School of Medicine Central South University Changsha China

7. Cancer Center, Union Hospital, Tongji Medical College Huazhong University of Science and Technology Wuhan China

Abstract

AbstractBackgroundTo develop a radiomics model based on chest computed tomography (CT) for the prediction of a pathological complete response (pCR) after neoadjuvant or conversion chemoimmunotherapy (CIT) in patients with non‐small cell lung cancer (NSCLC).MethodsPatients with stage IB–III NSCLC who received neoadjuvant or conversion CIT between September 2019 and July 2021 at Hunan Cancer Hospital, Xiangya Hospital, and Union Hospital were retrospectively collected. The least absolute shrinkage and selection operator (LASSO) were used to screen features. Then, model 1 (five radiomics features before CIT), model 2 (four radiomics features after CIT and before surgery) and model 3 were constructed for the prediction of pCR. Model 3 included all nine features of model 1 and 2 and was later named the neoadjuvant chemoimmunotherapy‐related pathological response prediction model (NACIP).ResultsThis study included 110 patients: 77 in the training set and 33 in the validation set. Thirty‐nine (35.5%) patients achieved a pCR. Model 1 showed area under the curve (AUC) = 0.65, 64% accuracy, 71% specificity, and 50% sensitivity, while model 2 displayed AUC = 0.81, 73% accuracy, 62% specificity, and 92% sensitivity. In comparison, NACIP yielded a good predictive value, with an AUC of 0.85, 81% accuracy, 81% specificity, and 83% sensitivity in the validation set.ConclusionNACIP may be a potential model for the early prediction of pCR in patients with NSCLC treated with neoadjuvant/conversion CIT.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Pulmonary and Respiratory Medicine,Oncology,General Medicine

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