[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
相关论文
共 50 条
  • [31] The efficiency of 18F-FDG PET-CT for predicting the major pathologic response to the neoadjuvant PD-1 blockade in resectable non-small cell lung cancer
    Tao, Xiuli
    Li, Ning
    Wu, Ning
    He, Jie
    Ying, Jianming
    Gao, Shugeng
    Wang, Shuhang
    Wang, Jie
    Wang, Zhijie
    Ling, Yun
    Tang, Wei
    Zhang, Zewei
    EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2020, 47 (05) : 1209 - 1219
  • [32] Predicting PD-L1 expression status in patients with non-small cell lung cancer using [18F]FDG PET/CT radiomics
    Xiaoqian Zhao
    Yan Zhao
    Jingmian Zhang
    Zhaoqi Zhang
    Lihua Liu
    Xinming Zhao
    EJNMMI Research, 13
  • [33] Predicting PD-L1 expression status in patients with non-small cell lung cancer using [18F]FDG PET/CT radiomics
    Zhao, Xiaoqian
    Zhao, Yan
    Zhang, Jingmian
    Zhang, Zhaoqi
    Liu, Lihua
    Zhao, Xinming
    EJNMMI RESEARCH, 2023, 13 (01)
  • [34] The prediction of response to immunotherapy in non-small cell lung cancer patients by 18F-FDG PET/CT
    Evangelista, Laura
    JOURNAL OF THORACIC DISEASE, 2019, 11 (11) : E221 - E223
  • [35] Predicative value of [18F]-FDG PET scan for pathological complete response to neoadjuvant chemotherapy in breast cancer
    Favier, L.
    Berriolo-Riedinger, A.
    Coudert, B.
    Touzery, C.
    Riedinger, J.
    Toubeau, M.
    Arnould, L.
    Brunotte, F.
    Fumoleau, P.
    JOURNAL OF CLINICAL ONCOLOGY, 2007, 25 (18)
  • [36] [18F]FDG PET/CT versus [18F]FDG PET/MRI in staging of non-small cell lung cancer: a head-to-head comparative meta-analysis
    Yu, Dandan
    Chen, Chaolin
    FRONTIERS IN MEDICINE, 2025, 11
  • [37] Evaluation of regional lymph node involvement in the staging of non-small cell lung cancer with 18F FDG PET/CT
    Keskin, M.
    EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2020, 47 (SUPPL 1) : S569 - S570
  • [38] Monitoring metabolic changes in non-small cell lung cancer during and after radiotherapy by [18F]FDG PET/CT
    Giovacchini, G.
    Picchio, M.
    Schipani, S.
    Landoni, C.
    Coradeschi, E.
    Gianolli, L.
    DiMuzio, N.
    Gilardi, M. C.
    Messa, C.
    Fazio, F.
    EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2006, 33 : S264 - S264
  • [39] Value Of [18F]FDG PET/CT In The Diagnosis Of Thoracic Lymph Node Metastasis In Non-Small Cell Lung Cancer
    Calderon Calvente, M.
    Alvarez Ruiz, S.
    Sangros Sahun, M.
    Nieto Morcillo, L.
    Guzman Prudencio, G.
    Diez Canseco, L. Del Barco
    Navarro Beltran, P.
    Falgas Lacueva, M.
    De la Cueva Barrao, L.
    Abos Olivares, D.
    EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2020, 47 (SUPPL 1) : S565 - S565
  • [40] Is 18F-FDG PET/CT Useful for the Early Prediction of Histopathologic Response to Neoadjuvant Erlotinib in Patients with Non-Small Cell Lung Cancer?
    Aukema, Tjeerd S.
    Kappers, Ingrid
    Olmos, Renato A. Valdes
    Codrington, Henk E.
    van Tinteren, Harm
    van Pel, Renee
    Klomp, Houke M.
    JOURNAL OF NUCLEAR MEDICINE, 2010, 51 (09) : 1344 - 1348