Gian Marco Petrianni

Dr. Gian Marco Petrianni

orcid

Research Focus & Metrics

Academic Career Length

5Years (2022-Present)

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

Representative Publications

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1 April 2023 in Journal of Gastrointestinal Oncology
Verified
Journal Article
Open access
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MFMichele Fiore
Michele Fiore
ACAlessandro Coppola
Alessandro Coppola
GPGian Marco Petrianni
Gian Marco Petrianni
PTPasquale Trecca
Pasquale Trecca
GDGabriele D’eRcole
Gabriele D’eRcole
SRSara Ramella
Sara Ramella
Review Article Advances in pre-treatment evaluation of pancreatic ductal adenocarcinoma: a narrative review Michele Fiore, Alessandro Coppola, Gian Marco Petrianni, Pasquale Trecca, Gabriele D’Ercole, Paola Cimini, Edy Ippolito, Damiano Caputo, Bruno Beomonte Zobel, Roberto Coppola, Sara Ramella

31 December 2022 in La radiologia medica
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Journal Article
Closed access
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VNValerio Nardone
Valerio Nardone
LBLuca Boldrini
Luca Boldrini
VSViola Salvestrini
Viola Salvestrini
CGCarlo Greco
Carlo Greco
GPGian Marco Petrianni
Gian Marco Petrianni
FFFrancesca De Felice
Francesca De Felice

27 June 2023 in La radiologia medica
Verified
Journal Article
Closed access
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GPGian Marco Petrianni
Gian Marco Petrianni
MFMichele Fiore
Michele Fiore
EOElena Onorati
Elena Onorati
GLGiammaria Liuzzi
Giammaria Liuzzi
MMMassimo Minerva
Massimo Minerva

10 November 2023 in European Journal of Surgical Oncology
Verified
Journal Article
Closed access
MFMichele Fiore
Michele Fiore
GPGian Marco Petrianni
Gian Marco Petrianni
GDGabriele D'Ercole
Gabriele D'Ercole
PTPasquale Trecca
Pasquale Trecca
SRSara Ramella
Sara Ramella

18 December 2024 in Journal of Clinical Medicine
Verified
Journal Article
Open access
PDF file
MFMichele Fiore
Michele Fiore
GPGian Marco Petrianni
Gian Marco Petrianni
GDGabriele D'Ercole
Gabriele D'Ercole
EOElena Onorati
Elena Onorati
PTPasquale Trecca
Pasquale Trecca
SRSara Ramella
Sara Ramella
Background: Pancreatic cancer, with its poor prognosis, is frequently diagnosed in elderly patients who may be ineligible for surgery or chemoradiation due to age or comorbidities. Stereotactic body radiotherapy (SBRT) offers a targeted approach by delivering precise, high-dose radiation to a limited volume in few fractions. This study aims to evaluate the efficacy and safety of SBRT in elderly pancreatic cancer patients. Methods: Patients with pancreatic cancer received SBRT using Volumetric Modulated Arc Therapy in schedules of five dose fractions tailored to the tolerance of adjacent tissues. Progression-free survival (PFS), local progression-free survival (LPFS), metastasis-free survival (MFS) and overall survival (OS) were analysed. Toxicities were graded according to the Common Terminology Criteria for Adverse Events (CTCAE) v5.0. Results: Median follow-up was 9.5 months (range, 4–37.2 months). The 1-year, 2-year and 3-year LPFS rates were 88%, 73% and 54%, respectively (median not reached). Median PFS, MFS and OS were 29.6 months, 32.6 months, and 24.1 months, respectively. SBRT was well tolerated with acute and late toxicity rates of 6% and 9%, respectively. Conclusionsd: SBRT appears to be an effective and safe option for elderly pancreatic cancer patients, achieving high local control with minimal toxicity.

14 May 2026 in Diagnostics
Verified
Journal Article
Open access
PDF file
MFMichele Fiore
Michele Fiore
ECErmanno Cordelli
Ermanno Cordelli
GPGian Marco Petrianni
Gian Marco Petrianni
GDGabriele D'Ercole
Gabriele D'Ercole
PTPasquale Trecca
Pasquale Trecca
SRSara Ramella
Sara Ramella
Background/Objectives: Early progression (EP) occurs in a subset of patients with locally advanced pancreatic cancer (LAPC), limiting the clinical benefit of treatment, and it remains difficult to predict. Methods: We developed a multiparametric predictive model integrating baseline 18F-FDG PET/CT radiomic features with clinical and biological data. A total of 242 radiomic features were extracted from each imaging modality (CT and PET), including first-order, gray-level co-occurrence matrix (GLCM), and local binary pattern (LBP-TOP) features, and combined with PET-derived metrics and clinical variables. Model development included cross-validation procedures and rigorous feature selection, followed by the training of a two-level decision tree classifier. Results: The model achieved an accuracy of 80.7% and an area under the curve (AUC) of 0.83. Integrated analysis of CT and PET texture enabled the identification of patients at high risk of EP prior to treatment initiation. Conclusions: PET/CT-based radiomic biomarkers, combined with clinical data, can non-invasively capture tumor heterogeneity and improve risk stratification in LAPC, supporting more personalized therapeutic decision-making.