Correlation between combining F–FDG PET/CT metabolic parameters and other clinical features and ALK or ROS1 fusion in patients with non-small-cell lung cancer
Creators
- 1. Department of Nuclear Medicine, Shanghai Chest Hospital, Shanghai Jiao Tong University (China)
- 2. Department of Radiology, Shanghai Chest Hospital, Shanghai Jiao Tong University (China)
Description
Our study intended to explore the association between combining F–FDG PET/CT metabolic parameters and other clinical features and anaplastic lymphoma kinase (ALK) or c-ros oncogene 1 (ROS1) fusion in non-small-cell lung cancer (NSCLC). Eight hundred and six patients with wild-type epidermal growth factor receptor (EGFR) mutation were screened for ALK or ROS1 fusion and subjected to F–FDG PET/CT prior to treatment at our hospital. The associations between ALK or ROS1 fusion and clinical characteristics and the PET/CT parameters were analyzed. Multivariate logistic regression analysis was performed to explore independent deterministic factors associated with ALK and ROS1 fusion. Eighty-two patients (11.7%) with ALK fusion were found. Multivariate analysis demonstrated that high pSUVmax ≥ 10.6, low primary tumor lesion glycolysis (pTLG) < 101.8, young age, nonsmoker status, and high carcinoembryonic antigen (CEA) level correlated with ALK fusion in NSCLC. The receiver operating characteristic (ROC) curve yielded the area under curve (AUC) values of 0.603 and 0.873 for high pSUVmax alone and the combination of the five factors, respectively. Twenty-six patients (5.6%) with ROS1 fusion were found. Multivariate analysis revealed that high pSUVmax ≥ 8.8, young age, and nonsmoker status correlated with ROS1 fusion in NSCLC. The ROC curve yielded AUC values of 0.662 and 0.813 for high pSUVmax alone and the combination of the three factors, respectively. The study indicated that combining F–FDG PET/CT metabolic parameters and other clinical parameters were correlated with ALK and ROS1 mutation in NSCLC patients and may help to refine the process of optimal patient selection to gene test for targeted therapy.
Availability note (English)
Available from: http://dx.doi.org/10.1007/s00259-019-04652-6Additional details
Identifiers
Publishing Information
- Journal Title
- European Journal of Nuclear Medicine and Molecular Imaging
- Journal Volume
- 47
- Journal Issue
- 5
- Journal Page Range
- p. 1183-1197
- ISSN
- 1619-7070
- CODEN
- EJNMA6
INIS
- Country of Publication
- Germany
- Country of Input or Organization
- Germany
- INIS RN
- 51082178
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- CORRELATIONS; FLUORINE 18; FLUORODEOXYGLUCOSE; GLYCOLYSIS; GROWTH FACTORS; LUNGS; LYMPHOMAS; MEGA BQ RANGE 100-1000; MULTIVARIATE ANALYSIS; MUTATIONS; ONCOGENES; PHOSPHOTRANSFERASES; POSITRON COMPUTED TOMOGRAPHY; RADIOPHARMACEUTICALS; RECEPTORS; REGRESSION ANALYSIS; SENSITIVITY; SPECIFICITY; UPTAKE
- Descriptors DEC
- ANTIMETABOLITES; BETA DECAY RADIOISOTOPES; BETA-PLUS DECAY RADIOISOTOPES; BODY; CHEMICAL REACTIONS; COMPUTERIZED TOMOGRAPHY; DECOMPOSITION; DIAGNOSTIC TECHNIQUES; DISEASES; DRUGS; EMISSION COMPUTED TOMOGRAPHY; ENZYMES; FLUORINE ISOTOPES; GENES; HOURS LIVING RADIOISOTOPES; IMMUNE SYSTEM DISEASES; ISOMERIC TRANSITION ISOTOPES; ISOTOPES; LABELLED COMPOUNDS; LIGHT NUCLEI; MATERIALS; MATHEMATICS; MEGA BQ RANGE; MEMBRANE PROTEINS; METABOLISM; MITOGENS; NANOSECONDS LIVING RADIOISOTOPES; NEOPLASMS; NUCLEI; ODD-ODD NUCLEI; ORGANIC COMPOUNDS; ORGANS; PHOSPHORUS-GROUP TRANSFERASES; PROTEINS; RADIOACTIVE MATERIALS; RADIOACTIVITY RANGE; RADIOISOTOPES; RESPIRATORY SYSTEM; STATISTICS; TOMOGRAPHY; TRANSFERASES