[18F]FDG PET-CT radiomics signature to predict pathological complete response to neoadjuvant chemoimmunotherapy in non-small cell lung cancer: a multicenter study

被引:5
|
作者
Yang, Minglei [1 ]
Li, Xiaoxiao [2 ]
Cai, Chuang [3 ]
Liu, Chunli [2 ]
Ma, Minjie [4 ]
Qu, Wendong [5 ]
Zhong, Sheng [6 ]
Zheng, Enkuo [1 ]
Zhu, Huangkai [1 ]
Jin, Feng [7 ]
Shi, Huazheng [2 ]
机构
[1] Ningbo No 2 Hosp, Dept Thorac Surg, Ningbo, Peoples R China
[2] Shanghai Universal Cloud Med Imaging Diagnost Ctr, Shanghai, Peoples R China
[3] Jiangsu Univ, Sch Comp Sci & Commun Engn, Zhenjiang, Jiangsu, Peoples R China
[4] Lanzhou Univ, Hosp 1, Dept Gastroenterol, Lanzhou, Gansu, Peoples R China
[5] Zunyi Med Univ, Dept Thorac Surg, Affiliated Hosp, Zunyi, Guizhou, Peoples R China
[6] Tailai Inc, Shanghai, Peoples R China
[7] Shandong Univ, Shandong Key Lab Infect Resp Dis, Shandong Publ Hlth Clin Ctr, Jinan, Shandong, Peoples R China
关键词
PET-CT; Radiomics; Non-small cell lung cancer; Chemoimmunotherapy; Pathological response; SINGLE-ARM; OPEN-LABEL; CHEMOTHERAPY; NIVOLUMAB;
D O I
10.1007/s00330-023-10503-8
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Objectives This study aims to develop and validate a radiomics model based on F-18-fluorodeoxyglucose positron emission tomography-computed tomography ([F-18]FDG PET-CT) images to predict pathological complete response (pCR) to neoadjuvant chemoimmunotherapy in non-small cell lung cancer (NSCLC).Materials and methods One hundred eighty-five patients receiving neoadjuvant chemoimmunotherapy for NSCLC at 5 centers from January 2019 to December 2022 were included and divided into a training cohort and a validation cohort. Radiomics models were constructed via the least absolute shrinkage and selection operator (LASSO) method. The performances of models were evaluated by the area under the receiver operating characteristic curve (AUC). In addition, genetic analyses were conducted to reveal the underlying biological basis of the radiomics score.Results After the LASSO process, 9 PET-CT radiomics features were selected for pCR prediction. In the validation cohort, the ability of PET-CT radiomics model to predict pCR was shown to have an AUC of 0.818 (95% confidence interval [CI], 0.711, 0.925), which was better than the PET radiomics model (0.728 [95% CI, 0.610, 0.846]), CT radiomics model (0.732 [95% CI, 0.607, 0.857]), and maximum standard uptake value (0.603 [95% CI, 0.473, 0.733]) (p < 0.05). Moreover, a high radiomics score was related to the upregulation of pathways suppressing tumor proliferation and the infiltration of antitumor immune cell.Conclusion The proposed PET-CT radiomics model was capable of predicting pCR to neoadjuvant chemoimmunotherapy in NSCLC patients.
引用
收藏
页码:4352 / 4363
页数:12
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