Francesco Spagnolo

ORCID: 0000-0003-3287-1225
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About
Contact & Profiles
Research Areas
  • Cancer Immunotherapy and Biomarkers
  • Diabetes Treatment and Management
  • Melanoma and MAPK Pathways
  • Cutaneous Melanoma Detection and Management
  • Pancreatic and Hepatic Oncology Research
  • CAR-T cell therapy research
  • Neutropenia and Cancer Infections
  • Immunotherapy and Immune Responses
  • Cancer Genomics and Diagnostics
  • Hyperglycemia and glycemic control in critically ill and hospitalized patients
  • Colorectal Cancer Treatments and Studies
  • Metabolism, Diabetes, and Cancer
  • Nonmelanoma Skin Cancer Studies
  • Brain Metastases and Treatment
  • Inflammatory Biomarkers in Disease Prognosis
  • Ocular Oncology and Treatments
  • Immune cells in cancer
  • Economic and Financial Impacts of Cancer
  • Computational Drug Discovery Methods
  • Lung Cancer Treatments and Mutations
  • Click Chemistry and Applications
  • Advanced Breast Cancer Therapies
  • Cancer and Skin Lesions
  • Cancer Treatment and Pharmacology
  • Chronic Lymphocytic Leukemia Research

Ospedale Policlinico San Martino
2016-2025

University of Genoa
2017-2024

Azienda Ospedaliera Pugliese Ciaccio
2022-2024

Alleanza Contro il Cancro
2012-2020

Ospedale San Paolo
2019

Istituti di Ricovero e Cura a Carattere Scientifico
2012-2017

National Cancer Research Institute
2016

Queen Mary University of London
2015

Mater Hospital
2015

Azienda Ospedaliera Universitaria Senese
2014

Clinical responses to ipilimumab are variable in terms of onset, magnitude and duration. Upfront identification patients who more likely or unlikely benefit from treatment is a major need.Prospectively collected data 720 advanced melanoma treated with 3 mg/kg within the Italian expanded access program were analyzed. The derived neutrophil-to-lymphocyte ratio (dNLR) was calculated baseline peripheral blood cell counts, receiver operating characteristic curve used evaluate best cutoff for this...

10.1093/annonc/mdw016 article EN publisher-specific-oa Annals of Oncology 2016-01-23

Background Concomitant medications, such as steroids, proton pump inhibitors (PPI) and antibiotics, might affect clinical outcomes with immune checkpoint inhibitors. Methods We conducted a multicenter observational retrospective study aimed at evaluating the impact of concomitant medications on outcomes, by weighing their associations baseline characteristics (including performance status, burden disease body mass index) underlying causes for prescription. This analysis included consecutive...

10.1136/jitc-2020-001361 article EN cc-by-nc Journal for ImmunoTherapy of Cancer 2020-11-01

Limited prospective data are available on sequential immunotherapy and BRAF/MEK inhibition for BRAFV600-mutant metastatic melanoma.SECOMBIT is a randomized, three-arm, noncomparative phase II trial (ClinicalTrials.gov identifier: NCT02631447). Patients with untreated, melanoma from 37 sites in nine countries were randomly assigned to arm A (encorafenib [450 mg orally once daily] plus binimetinib [45 twice until progressive disease [PD] -> ipilimumab nivolumab [ipilimumab 3 mg/kg every weeks...

10.1200/jco.21.02961 article EN Journal of Clinical Oncology 2022-09-01

Abstract No prospective data were available prior to 2021 inform selection between combination BRAF and MEK inhibition versus dual blockade of programmed cell death protein-1 (PD-1) cytotoxic T lymphocyte antigen-4 (CTLA-4) as first-line treatment options for BRAFV 600-mutant melanoma. SECOMBIT (NCT02631447) was a randomized, three-arm, noncomparative phase II trial in which patients randomized one two sequences with immunotherapy or targeted therapy first, third arm an 8-week induction...

10.1038/s41467-023-44475-6 article EN cc-by Nature Communications 2024-01-02

Clinical trials frequently include multiple end points that mature at different times. The initial report, typically based on the primary point, may be published when key planned co-primary or secondary analyses are not yet available. Trial Updates provide an opportunity to disseminate additional results from studies, in JCO elsewhere, for which point has already been reported. Pembrolizumab adjuvant therapy was shown significantly improve recurrence-free survival (RFS) and distant...

10.1200/jco.23.02355 article EN cc-by-nc-nd Journal of Clinical Oncology 2024-03-07

In recent years, advances in melanoma treatment have renewed patient hope. This comprehensive review emphasizes the evolving landscape, particularly highlighting first-line strategies and interplay between immune-checkpoint inhibitors (ICIs) targeted therapies. Ipilimumab plus nivolumab has achieved best median overall survival, exceeding 70 months. However, introduction of new ICIs, like relatlimab, added complexity to therapy decisions. Our aim is guide clinicians making personalized...

10.1016/j.critrevonc.2024.104276 article EN cc-by-nc-nd Critical Reviews in Oncology/Hematology 2024-01-29

Abstract Patients with melanoma brain metastases have a poor prognosis and historically been excluded from clinical trials. The Expanded Access Program (EAP) provided an opportunity to evaluate the feasibility of ipilimumab (3 mg/kg every 3 weeks for four doses) in patients stage (unresectable) or 4 asymptomatic metastases, who had failed did not tolerate previous treatments no other therapeutic option available. Tumor assessments were conducted at baseline week 12 using immune-related...

10.1007/s11060-014-1400-y article EN cc-by Journal of Neuro-Oncology 2014-02-16

Abstract Purpose: No evidence exists as to whether type 2 diabetes mellitus (T2DM) impairs clinical outcome from immune checkpoint inhibitors (ICI) in patients with solid tumors. Experimental Design: In a large cohort of ICI recipients treated at 21 institutions June 2014 2020, we studied on glucose-lowering medications (GLM) for T2DM had shorter overall survival (OS) and progression-free (PFS). We used targeted transcriptomics subset explore differences the tumor microenvironment (TME) or...

10.1158/1078-0432.ccr-22-3116 article EN Clinical Cancer Research 2023-05-01
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