FDG PET/CT radiomics as a tool to differentiate between reactive axillary lymphadenopathy following COVID-19 vaccination and metastatic breast cancer axillary lymphadenopathy. A pilot study
Creators
- 1. Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv (Israel)
- 2. Department of Diagnostic Imaging, Chaim Sheba Medical Center, 2 Sheba Road, 5266202, Ramat Gan (Israel)
- 3. ARC Center for Digital Innovation, Chaim Sheba Medical Center, Ramat Gan (Israel)
- 4. Department of Radiology, Massachusetts General Hospital, Harvard Medical School, Boston, MA (United States)
Description
To evaluate if radiomics with machine learning can differentiate between F-18-fluorodeoxyglucose (FDG)-avid breast cancer metastatic lymphadenopathy and FDG-avid COVID-19 mRNA vaccine-related axillary lymphadenopathy. We retrospectively analyzed FDG-positive, pathology-proven, metastatic axillary lymph nodes in 53 breast cancer patients who had PET/CT for follow-up or staging, and FDG-positive axillary lymph nodes in 46 patients who were vaccinated with the COVID-19 mRNA vaccine. Radiomics features (110 features classified into 7 groups) were extracted from all segmented lymph nodes. Analysis was performed on PET, CT, and combined PET/CT inputs. Lymph nodes were randomly assigned to a training (n = 132) and validation cohort (n = 33) by 5-fold cross-validation. K-nearest neighbors (KNN) and random forest (RF) machine learning models were used. Performance was evaluated using an area under the receiver-operator characteristic curve (AUC-ROC) score. Axillary lymph nodes from breast cancer patients (n = 85) and COVID-19-vaccinated individuals (n = 80) were analyzed. Analysis of first-order features showed statistically significant differences (p < 0.05) in all combined PET/CT features, most PET features, and half of the CT features. The KNN model showed the best performance score for combined PET/CT and PET input with 0.98 (± 0.03) and 0.88 (± 0.07) validation AUC, and 96% (± 4%) and 85% (± 9%) validation accuracy, respectively. The RF model showed the best result for CT input with 0.96 (± 0.04) validation AUC and 90% (± 6%) validation accuracy. Radiomics features can differentiate between FDG-avid breast cancer metastatic and FDG-avid COVID-19 vaccine-related axillary lymphadenopathy. Such a model may have a role in differentiating benign nodes from malignant ones. Patients who were vaccinated with the COVID-19 mRNA vaccine have shown FDG-avid reactive axillary lymph nodes in PET-CT scans. We evaluated if radiomics and machine learning can distinguish between FDG-avid metastatic axillary lymphadenopathy in breast cancer patients and FDG-avid reactive axillary lymph nodes. Combined PET and CT radiomics data showed good test AUC (0.98) for distinguishing between metastatic axillary lymphadenopathy and post-COVID-19 vaccine-associated axillary lymphadenopathy. Therefore, the use of radiomics may have a role in differentiating between benign from malignant FDG-avid nodes.
Availability note (English)
Available from: http://dx.doi.org/10.1007/s00330-022-08725-3Additional details
Identifiers
Publishing Information
- Journal Title
- European Radiology (Internet)
- Journal Volume
- 32
- Journal Issue
- 9
- Journal Page Range
- p. 5921-5929
- ISSN
- 1432-1084
- CODEN
- EURAE3
INIS
- Country of Publication
- Germany
- Country of Input or Organization
- Germany
- INIS RN
- 53099290
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- ACCURACY; CARCINOMAS; CORONAVIRUSES; FLUORINE 18; FLUORODEOXYGLUCOSE; IMAGE PROCESSING; LYMPH NODES; MACHINE LEARNING; MAMMARY GLANDS; MESSENGER-RNA; METASTASES; PATHOLOGY; POSITRON COMPUTED TOMOGRAPHY; RADIOMICS; TRAINING; VACCINES; VALIDATION
- Descriptors DEC
- ALGORITHMS; ANTIMETABOLITES; ARTIFICIAL INTELLIGENCE; BETA DECAY RADIOISOTOPES; BETA-PLUS DECAY RADIOISOTOPES; BODY; COMPUTERIZED TOMOGRAPHY; DIAGNOSTIC TECHNIQUES; DISEASES; DRUGS; EDUCATION; EMISSION COMPUTED TOMOGRAPHY; FLUORINE ISOTOPES; GLANDS; HOURS LIVING RADIOISOTOPES; INFECTIOUS DISEASES; ISOMERIC TRANSITION ISOTOPES; ISOTOPES; LEARNING; LIGHT NUCLEI; LYMPHATIC SYSTEM; MATHEMATICAL LOGIC; MEDICINE; MICROORGANISMS; NANOSECONDS LIVING RADIOISOTOPES; NEOPLASMS; NUCLEAR MEDICINE; NUCLEI; NUCLEIC ACIDS; ODD-ODD NUCLEI; ORGANIC COMPOUNDS; ORGANS; PARASITES; PROCESSING; RADIOISOTOPES; RADIOLOGY; RNA; TESTING; TOMOGRAPHY; VIRAL DISEASES; VIRUSES; ZOONOTIC DISEASES