Claudia Fabiani

Dr. Claudia Fabiani

Ophthalmology Unit, University of Siena, Siena, Tuscany, Italy
orcid

Research Focus & Metrics

Academic Career Length

31Years (1996-Present)

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

Representative Publications

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16 December 2016 in Clinical Rheumatology
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Journal Article
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Claudia FabianiClaudia Fabiani
Claudia Fabiani
AVAntonio Vitale
Antonio Vitale
GEGiacomo Emmi
Giacomo Emmi
GLGiuseppe Lopalco
Giuseppe Lopalco
LVLorenzo Vannozzi
Lorenzo Vannozzi
LCLuca Cantarini
Luca Cantarini

1 August 2009 in Experimental Eye Research
Verified
Journal Article
Closed access
Claudia FabianiClaudia Fabiani
Claudia Fabiani
SBStefano Barabino
Stefano Barabino
SRSaadia Rashid
Saadia Rashid
MDM. Reza Dana
M. Reza Dana

16 November 2016 in Clinical Rheumatology
Verified
Journal Article
Closed access
PDF file
Claudia FabianiClaudia Fabiani
Claudia Fabiani
AVAntonio Vitale
Antonio Vitale
GEGiacomo Emmi
Giacomo Emmi
LVLorenzo Vannozzi
Lorenzo Vannozzi
GLGiuseppe Lopalco
Giuseppe Lopalco
LCLuca Cantarini
Luca Cantarini

17 May 2018 in Clinical Rheumatology
Verified
Journal Article
Closed access
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FRfor the “Working Group” of Systemic Autoinflammatory Diseases of SIR (Italian Society of Rheumatology)
for the “Working Group” of Systemic Autoinflammatory Diseases of SIR (Italian Society of Rheumatology)
JSJurgen Sota
Jurgen Sota
AVAntonio Vitale
Antonio Vitale
AIAntonella Insalaco
Antonella Insalaco
PSPaolo Sfriso
Paolo Sfriso
LCLuca Cantarini
Luca Cantarini

24 October 2016 in Frontiers in Pharmacology
Verified
Journal Article
Open access
PDF file
AVAntonio Vitale
Antonio Vitale
AIAntonella Insalaco
Antonella Insalaco
PSPaolo Sfriso
Paolo Sfriso
GLGiuseppe Lopalco
Giuseppe Lopalco
GEGiacomo Emmi
Giacomo Emmi
LCLuca Cantarini
Luca Cantarini
Background: Interleukin (IL)-1 inhibitors have been suggested as possible therapeutic options in a large number of old and new clinical entities characterized by an IL-1 driven pathogenesis. Objectives: To perform a nationwide snapshot of the on-label and off-label use of anakinra (ANA) and canakinumab (CAN) for different conditions both in children and adults. Methods: We retrospectively collected demographic, clinical, and therapeutic data from both adult and pediatric patients treated with IL-1 inhibitors from January 2008 to July 2016. Results: Five hundred and twenty-six treatment courses given to 475 patients (195 males, 280 females; 111 children and 364 adults) were evaluated. ANA was administered in 421 (80.04%) courses, CAN in 105 (19.96%). Sixty-two (32.1%) patients had been treated with both agents. IL-1 inhibitors were employed in 38 different indications (37 with ANA, 16 with CAN). Off-label use was more frequent for ANA than CAN (p < 0.0001). ANA was employed as first-line biologic approach in 323 (76.7%) cases, while CAN in 37 cases (35.2%). IL-1 inhibitors were associated with corticosteroids in 285 (54.18%) courses and disease modifying anti-rheumatic drugs (DMARDs) in 156 (29.65%). ANA dosage ranged from 30 to 200 mg/day (or 1.0–2.0 mg/kg/day) among adults and 2–4 mg/kg/day among children; regarding CAN, the most frequently used posologies were 150mg every 8 weeks, 150mg every 4 weeks and 150mg every 6 weeks. The frequency of failure was higher among patients treated with ANA at a dosage of 100 mg/day than those treated with 2 mg/kg/day (p = 0.03). Seventy-six patients (14.4%) reported an adverse event (AE) and 10 (1.9%) a severe AE. AEs occurred more frequently after the age of 65 compared to both children and patients aged between 16 and 65 (p = 0.003 and p = 0.03, respectively). Conclusions: IL-1 inhibitors are mostly used off-label, especially ANA, during adulthood. The high frequency of good clinical responses suggests that IL-1 inhibitors are used with awareness of pathogenetic mechanisms; adult healthcare physicians generally employ standard dosages, while pediatricians are more prone in using a weight-based posology. Dose adjustments and switching between different agents showed to be effective treatment strategies. Our data confirm the good safety profile of IL-1 inhibitors.

20 April 2018 in Arthritis & Rheumatology
Verified
Journal Article
Closed access
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GEGiacomo Emmi
Giacomo Emmi
AVAntonio Vitale
Antonio Vitale
ESElena Silvestri
Elena Silvestri
MBMaria Boddi
Maria Boddi
Matteo BecattiMatteo Becatti
Matteo Becatti
DPDomenico Prisco
Domenico Prisco