Publications by authors named "Rosa Fonti"

: The aim of the present study was to test whether a parameter reflecting tumor dissemination (Dmax), derived from basal 18F-FDG PET/CT, may predict clinical outcome in patients with advanced non-small-cell lung cancer (NSCLC). : A total of 78 patients (55 men, 23 women) with stage III and IV NSCLC who had undergone whole-body 18F-FDG PET/CT scan at diagnosis were included in this study. Imaging parameters of primary lung tumors along with total MTV (MTV) and whole-body TLG (TLG) of all malignant lesions were determined.

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In multiple myeloma (MM) bone marrow infiltration by monoclonal plasma cells can occur in both focal and diffuse manner, making staging and prognosis rather difficult. The aim of our study was to test whether texture analysis of 18 F-2-deoxy-d-glucose positron emission tomography/computed tomography (18F-FDG PET/CT) images can predict survival in MM patients. Forty-six patients underwent 18 F-FDG-PET/CT before treatment.

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The aim of our study was to predict the occurrence of distant metastases in non-small-cell lung cancer (NSCLC) patients using machine learning methods and texture analysis of F-labeled 2-deoxy-d-glucose Positron Emission Tomography/Computed Tomography {[F]FDG PET/CT} images. In this retrospective and single-center study, we evaluated 79 patients with advanced NSCLC who had undergone [F]FDG PET/CT scan at diagnosis before any therapy. Patients were divided into two independent training ( = 44) and final testing ( = 35) cohorts.

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Purpose The aim of the present study was to test whether the coefficient of variation (CoV) of F-FDG PET/CT images of metastatic lymph nodes and primary tumors may predict clinical outcome in patients with advanced non-small cell lung cancer (NSCLC). Materials and Methods Fifty-eight NSCLC patients who had undergone F-FDG PET/CT at diagnosis were evaluated. SUVmax, SUVmean, CoV, MTV and TLG were determined in targeted lymph nodes and corresponding primary tumors along with Total MTV (MTV) and Whole-Body TLG (TLG) of all malignant lesions.

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We investigated the role of Coefficient of Variation (CoV), a first-order texture parameter derived from F-FDG PET/CT, in the prognosis of Non-Small Cell Lung Cancer (NSCLC) patients. Eighty-four patients with advanced NSCLC who underwent F-FDG PET/CT before therapy were retrospectively studied. SUVmax, SUVmean, CoV, total Metabolic Tumor Volume (MTV) and whole-body Total Lesion Glycolysis (TLG) were determined by an automated contouring program (SUV threshold at 2.

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Gastro-entero-pancreatic neuroendocrine neoplasms (GEP-NENs) constitute an ideal target for radiolabeled somatostatin analogs. The theragnostic approach is able to combine diagnosis and therapy by the identification of a molecular target that can be diagnosed and treated with the same radiolabeled compound. During the last years, advances in functional imaging with the introduction of somatostatin analogs and peptide receptor radionuclide therapy, have improved the diagnosis and treatment of GEP-NENs.

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COVID-19 pandemic had a great impact on health systems and cancer care worldwide. Patients with cancer who develop COVID-19 are at high risk of severe outcomes and clarifying the determinants of such vulnerability of cancer patients would be of great clinical benefit. While the mechanisms of SARS-CoV-2 infection have been elucidated, the pathogenetic pathways leading to severe manifestations of the disease are largely unknown.

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We evaluated the impact of liposomal doxorubicin (NPLD) supercharge-containing therapy on interim fluorodeoxyglucose positron emission tomography (interim-FDG-PET) responses in high-risk diffuse large B-cell lymphoma (DLBCL) or classical Hodgkin lymphoma (c-HL). In this phase II study (2016-2021), 81 adult patients with advanced-stage DLBCL (n = 53) and c-HL (n = 28) received front-line treatment with R-COMP-dose-intensified (DI) and MBVD-DI. R-COMP-DI consisted of 70 mg/m of NPLD plus standard rituximab, cyclophosphamide, vincristine and prednisone for three cycles (followed by three cycles with NPLD de-escalated at 50 mg/m ); MBVD-DI consisted of 35 mg/m of NPLD plus standard bleomycin, vinblastine and dacarbazine for two cycles (followed by four cycles with NPLD de-escalated at 25 mg/m ).

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High levels of somatostatin receptor subtype 2 (SSTR2) are a prerequisite for therapy with unlabeled or labeled somatostatin analogs. However, it is still unclear how the heterogeneity of SSTR2 expression may affect tumor response to therapy. The aim of our study was to test the ability of an imaging parameter such as coefficient of variation (CoV) derived from PET/CT with Ga-peptides in the evaluation and quantification of the heterogeneity of SSTR2 expression within primary and metastatic lesions of patients with neuroendocrine tumors.

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  • Researchers tested if targeting glucose metabolism and oncogene drivers together could improve the effectiveness of tyrosine kinase inhibitors (TKIs) in non-small cell lung cancer (NSCLC) cells.
  • They specifically downregulated pyruvate dehydrogenase kinase 1 (PDK1) in NSCLC cell lines and treated them with various TKIs to assess changes in metabolism and apoptosis.
  • Results showed that while PDK1 knockdown alone didn't significantly alter glucose metabolism, it enhanced mitochondrial respiration and apoptosis when combined with TKIs, indicating that targeting PDK1 could boost TKI efficacy by disrupting key protein complexes.
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  • Notch1 is important for the transition of cells during cancer progression (EMT) and helps maintain cancer stem cells, suggesting it plays a significant role in lung cancer dynamics.
  • The study investigated whether high levels of activated Notch1 in lung cancer cells could shift their reliance from the EGFR pathway to the Notch1 pathway, potentially leading to resistance against EGFR inhibitors.
  • Results showed that tumor spheres (cancer stem cells) exhibited higher resistance to EGFR inhibitors, with increased Notch1 signaling and decreased EGFR levels, indicating a possible mechanism behind the observed therapeutic resistance in NSCLC.
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Despite the recent advances in lung cancer biology, molecular pathology, and treatment, this malignancy remains the leading cause of cancer-related death worldwide and non-small cell lung cancer (NSCLC) is the most common form found at diagnosis. Accurate staging of the disease is a fundamental prognostic factor that correctly predicts progression-free (PFS) and overall survival (OS) of NSCLC patients. However, outcome of patients within each TNM staging group can change widely highlighting the need to identify additional prognostic biomarkers to better stratify patients on the basis of risk.

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  • The transition of cancer cells from an epithelial to a mesenchymal state during EMT is tied to their invasiveness and is linked to metastasis and treatment failures.
  • Liquid biopsy is a non-invasive method that helps analyze tumor components in body fluids, offering insights into how cancer progresses and spreads.
  • This review emphasizes using liquid biopsy in lung cancer to identify EMT characteristics, understand how invasive traits develop, and find new therapeutic targets.
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Recently, newer therapies such as immunotherapy have been increasingly used in the treatment of several tumors, including advanced melanoma. In particular, several studies showed that the combination of ipilimumab, an anti-Cytotoxic T-lymphocyte Associated Protein 4 (CTLA-4) monoclonal antibody and nivolumab, an anti-Programmed Death 1 (PD-1) monoclonal antibody, leads to improved survival in patients with metastatic melanoma. Despite that, immunotherapeutic agents may not reach therapeutic concentration in the brain due to the blood-brain barrier.

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Article Synopsis
  • Novel immunotherapy strategies like immune checkpoint blockade show promise in cancer treatment but only a small percentage of patients experience long-term success, highlighting the need for better patient selection.
  • *Despite various proposed biomarkers, none reliably predict which patients will respond to these treatments, suggesting the necessity for improved methods.
  • *Preclinical imaging studies focusing on developing tracers for visualizing immunotherapy targets may provide effective predictive biomarkers, and selecting appropriate animal models is crucial for translating these findings to clinical settings.
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  • In multiple myeloma (MM) patients, the use of 18F-FDG-PET/CT imaging helps track disease spread and assess metabolic tumor burden through visual and volumetric measures.
  • A study of 47 stage IIIA patients revealed significant differences in various parameters like maximum standardized uptake value and metabolic tumor volume (MTV) between those who experienced disease progression or death and those who did not.
  • The findings suggest that a specific MTV cutoff of 39.4 ml can effectively predict progression-free survival (PFS) and overall survival (OS), highlighting the importance of volume-based analysis in managing MM.
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Objective: Metabolic tumor volume (MTV) and total lesion glycolysis (TLG) are imaging parameters derived from 18F-FDG PET/CT that have been proposed for risk stratification of cancer patients. The aim of our study was to test whether these whole-body volumetric imaging parameters may predict outcome in patients with non-small cell lung cancer (NSCLC).

Methods: Sixty-five patients (45 men, 20 women; mean age ± SD, 65 ± 12 years), with histologically proven NSCLC who had undergone 18F-FDG PET/CT scan before any therapy, were included in the study.

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  • Preclinical imaging with radiolabeled probes is crucial for noninvasive testing of the efficacy of targeted cancer therapies and for identifying imaging markers that help monitor treatment responses in patients.
  • The review emphasizes the importance of targeting specific patient populations that express genetic alterations to maximize the success of clinical trials for these therapies.
  • Studies using various radiolabeled tracers have shown potential in assessing tumor responses, overcoming drug resistance, and facilitating patient selection for immunotherapy based on imaging results.
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The progressive integration of positron emission tomography/computed tomography (PET/CT) imaging in radiation therapy has its rationale in the biological intertumoral and intratumoral heterogeneity of malignant lesions that require the individual adjustment of radiation dose to obtain an effective local tumor control in cancer patients. PET/CT provides information on the biological features of tumor lesions such as metabolism, hypoxia, and proliferation that can identify radioresistant regions and be exploited to optimize treatment plans. Here, we provide an overview of the basic principles of PET-based target volume selection and definition using F-fluorodeoxyglucose (F-FDG) and then we focus on the emerging strategies of dose painting and adaptive radiotherapy using different tracers.

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  • Researchers tested if the drug imatinib could change how leukemia cells fueled themselves by altering key enzymes in glucose metabolism and mitochondrial function.
  • After treating leukemia cells with imatinib, they observed decreased levels of proteins that promote glycolysis and increased markers of oxidative phosphorylation.
  • These changes resulted in reduced glucose consumption and lactate production, while increasing ATP levels, suggesting a potential new strategy for targeting both BCR-ABL and mitochondrial functions in leukemia treatment.*
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  • Researchers tested different cancer cell lines to see how well they could attach to NETs, focusing on the expression of various integrins.
  • They discovered that certain integrins, particularly α5β1, αvβ3, and αvβ5, improve cancer cell adhesion to NETs, while low levels of α5β1 hinder it; a cyclic peptide was found to block this adhesion by competing with fibronectin in NETs.
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Background: We evaluated the role of [18F]FDG PET/CT in tumor response assessment and prognosis of primary extranodal lymphoma (PEL) patients.

Methods: We examined retrospectively, 56 PEL patients: 31 with aggressive diffuse large B cell lymphoma (DLBCL) and 25 with indolent lymphoma (20 mucosa-associated lymphoid tissue lymphoma and five follicular lymphoma). All patients had undergone [18F]FDG PET/CT at diagnosis (PET-I) and 50 of them also after therapy (PET-II).

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  • The study aimed to evaluate how well F-fluorothymidine (F-FLT) PET/CT imaging can identify the effects of combining EGFR and MET inhibitors in treating non-small cell lung cancer (NSCLC).
  • Researchers treated NSCLC cells and mice with these inhibitors individually and in combination, and observed significant decreases in tumor viability and F-FLT uptake with the combination treatment, indicating better effectiveness.
  • The enhanced treatment effectiveness was linked to the inositol trisphosphate receptor type 3 (IP3R3), which interacted with K-Ras, revealing a mechanism for the improved efficacy of the drug combination.
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Purpose: Medullary thyroid cancer (MTC) is a neuroendocrine tumour of the thyroid C cells. Pasireotide, a multi-receptor targeted somatostatin analogue, and everolimus, an inhibitor of mTOR, showed antitumour properties in neuroendocrine tumours. Aim of this study was to evaluate pasireotide alone and in combination with everolimus in patients with MTC.

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