Giuseppe Cardano

Dr. Giuseppe Cardano

orcid

Research Focus & Metrics

Academic Career Length

7Years (2020-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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27 May 2021 in La radiologia medica
Verified
Journal Article
Open access
PDF file
NCNicolò Cardobi
Nicolò Cardobi
Giulio BenettiGiulio Benetti
Giulio Benetti
GCGiuseppe Cardano
Giuseppe Cardano
CACinzia Arena
Cinzia Arena
CMClaudio Micheletto
Claudio Micheletto
SMStefania Montemezzi
Stefania Montemezzi
Purpose: To classify COVID-19, COVID-19-like and non-COVID-19 interstitial pneumonia using lung CT radiomic features. Material and Methods: CT data of 115 patients with respiratory symptoms suspected for COVID-19 disease were retrospectively analyzed. Based on the results of nasopharyngeal swab, patients were divided into two main groups, COVID-19 positive (C +) and COVID-19 negative (C−), respectively. C− patients, however, presented with interstitial lung involvement. A subgroup of C−, COVID-19-like (CL), were considered as highly suggestive of COVID pneumonia at CT. Radiomic features were extracted from the whole lungs. A dual machine learning (ML) model approach was used. The first one excluded CL patients from the training set, eventually included on the test set. The second model included the CL patients also in the training set. Results: The first model classified C + and C− pneumonias with AUC of 0.83. CL median response (0.80) was more similar to C + (0.92) compared to C− (0.17). Radiomic footprints of CL were similar to the C + ones (possibly false negative swab test). The second model, however, merging C + with CL patients in the training set, showed a slight decrease in classification performance (AUC = 0.81). Conclusion: Whole lung ML models based on radiomics can classify C + and C− interstitial pneumonia. This may help in the correct management of patients with clinical and radiological stigmata of COVID-19, however presenting with a negative swab test. CL pneumonia was similar to C + pneumonia, albeit with slightly different radiomic footprints.

30 October 2020 in European Radiology
Verified
Journal Article
Open access
PDF file
SMStefania Montemezzi
Stefania Montemezzi
GCGiuseppe Cardano
Giuseppe Cardano
SSSilvia Storer
Silvia Storer
NCNicolò Cardobi
Nicolò Cardobi
CCCarlo Cavedon
Carlo Cavedon
LCLucia Camera
Lucia Camera
Objectives: This study evaluated the feasibility of DWI for lesion targeting in MRI-guided breast biopsies. Furthermore, it assessed device positioning on DWI during biopsy procedures. Methods: A total of 87 biopsy procedures (5/87 bilateral) consecutively performed between March 2019 and June 2020 were retrospectively reviewed: in these procedures, a preliminary DWI sequence (b = 1300 s/mm2) was acquired to assess lesion detectability. We included 64/87 procedures on lesions detectable at DWI; DWI sequences were added to the standard protocol to localize lesion and biopsy device and to assess the site marker correct positioning. Results: Mass lesions ranged from 5 to 48 mm, with a mean size of 10.7 mm and a median size of 8 mm. Non-mass lesions ranged from 7 to 90 mm, with a mean size of 33.9 mm and a median size of 31 mm. Positioning of the coaxial system was confirmed on both T1-weighted and DWI sequences. At DWI, the biopsy needle was detectable in 62/64 (96.9%) cases; it was not visible in 2/64 (3.1%) cases. The site marker was always identified using T1-weighted imaging; a final DWI sequence was acquired in 44/64 cases (68.8%). In 42/44 cases (95.5%), the marker was recognizable at DWI. Conclusions: DWI can be used as a cost-effective, highly reliable technique for targeting both mass and non-mass lesions, with a minimum size of 5 mm, detectable at pre-procedural DWI. DWI is also a feasible technique to localize the biopsy device and to confirm the deployment of the site marker. Key Points: • MRI-guided breast biopsy is performed in referral centers by an expert dedicated staff, based on prior MR imaging; contrast agent administration is usually needed for lesion targeting. • DWI represents a feasible, highly reliable technique for lesion targeting, avoiding contrast agent administration. • DWI allows a precise localization of both biopsy needle device and site marker.

24 February 2025 in Applied Sciences
Verified
Journal Article
Open access
PDF file
MVMarina Fedon Vocaturo
Marina Fedon Vocaturo
LALuisa Altabella
Luisa Altabella
GCGiuseppe Cardano
Giuseppe Cardano
SMStefania Montemezzi
Stefania Montemezzi
CCCarlo Cavedon
Carlo Cavedon
In the era of precision medicine, increasing importance is given to machine learning (ML) applications. In breast cancer, advanced analyses, such as the radiomic process, characterise tumours and predict therapy responses. Breast magnetic resonance imaging (MRI) plays a key role in screening, staging, and treatment monitoring. Lesion segmentation on MRI is essential both to assess tumour growth and as a baseline for radiomic feature extraction. Manual segmentation is time-consuming and prone to inter-operator variability, limiting access to large labelled datasets and robust analyses. The use of ML for breast lesion segmentation on MRI has been investigated through a systematic review of PubMed, exploring studies published over the last 10 years. Results are compared in terms of performance, primarily using the Dice score. Early unsupervised methods achieved a mean Dice score of ∼0.75, surpassing traditional supervised methods (∼0.70). In contrast, deep learning (DL) approaches based on U-Net achieved higher average scores of 0.79. Further customised supervised DL approaches reached a mean Dice score of ∼0.83. However, there is still a gap in research on unsupervised DL techniques, which could help reduce bias and human variability. Future work may also explore multiparametric and multitechnique data, integrating more representative samples, including non-mass lesions.

19 January 2022 in Physica Medica
Verified
Journal Article
Open access
GBG. Benetti
G. Benetti
NCNicolò Cardobi
Nicolò Cardobi
GCGiuseppe Cardano
Giuseppe Cardano
CAC. Arena
C. Arena
CMClaudio Micheletto
Claudio Micheletto
CCCarlo Cavedon
Carlo Cavedon