Angelo Ruggiero

Dr. Angelo Ruggiero

University of Naples Federico II
orcid

Research Focus & Metrics

Academic Career Length

34Years (1993-Present)

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

Representative Publications

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13 October 2021 in Clinical and Experimental Dermatology
Verified
Journal Article
Open access
PDF file
ARAngelo Ruggiero
Angelo Ruggiero
GFG. Fabbrocini
G. Fabbrocini
ECE. Cinelli
E. Cinelli
SGS. S. Ocampo Garza
S. S. Ocampo Garza
Elisa CamelaElisa Camela
Elisa Camela
MMMatteo Megna
Matteo Megna
Background Elderly patients (≥65 years) represent an increasing rate of psoriatic patients, 15% have moderate-to-severe disease. Biologics are being frequently used even if safety and efficacy data are limited. Objective Evaluate and compare guselkumab, risankizumab, and tildrakizumab safety and efficacy in real-word-practice in elderly patients. Methods A 40/44 weeks single-center retrospective study enrolled patients aged≥65 years suffering from moderate-to-severe plaque-psoriasis, treated with guselkumab, risankizumab, or tildrakizumab. Results Thirty-four patients were enrolled (n=20 guselkumab; n=8 risankizumab; n=6 tildrakizumab). At week 4, 29.4% reached PASI90 and 8.8% PASI100; at week 28, PASI90 and PASI100 were observed in 58.8% and 29.4%, respectively. At week 40-44, data are available only for guselkumab and risankizumab groups in which 71.4% reached PASI90 and 53.5% PASI100. Four patients (11.7%) discontinued treatment. No significant differences were found among groups. Limitations Retrospective nature of the study, small sample size, non-equal follow-up duration among the groups, lower number of tildrakizumab patients, and higher components of guselkumab (different commercialization date). Conclusion Anti-IL-23s are promising, safe, and effective treatment options in elderlies without significant difference among them. However, more data are needed to confirm our results and to understand their role in the management of these more fragile patients.

16 August 2022 in Clinical, Cosmetic and Investigational Dermatology
Verified
Journal Article
Open access
PDF file
ARAngelo Ruggiero
Angelo Ruggiero
VPVincenzo Picone
Vincenzo Picone
Fabrizio MartoraFabrizio Martora
Fabrizio Martora
GFGabriella Fabbrocini
Gabriella Fabbrocini
MMMatteo Megna
Matteo Megna
Interleukin (IL)-23 inhibitors, guselkumab, risankizumab, and tildrakizumab, represent the latest class of biologics approved for the treatment of moderate-to-severe psoriasis. Since their approval numerous real-life studies were published on anti-IL-23 use in routine clinical practice. Indeed, real-life data are important to improve the dermatological decision-making process, including patients who are typically excluded from clinical trials, such as subjects suffering from several comorbidities, subjects on polypharmacy, as well as multifailure patients. Herein, we performed a comprehensive literature review about real-life data available on guselkumab, risankizumab, and tildrakizumab. Real-life data of anti-IL-23 seem to confirm the promising results of IL-23 shown by clinical trials, highlighting the efficacy and safety profiles of this new class of biologics also in clinical practice.

29 May 2022 in Journal of Dermatological Treatment
Verified
Journal Article
Closed access
MMMatteo Megna
Matteo Megna
NTNello Tommasino
Nello Tommasino
LPLuca Potestio
Luca Potestio
TBTeresa Battista
Teresa Battista
ARAngelo Ruggiero
Angelo Ruggiero
LGLucia Genco
Lucia Genco
Guselkumab, tildrakizumab and risankizumab, acting on interleukin(IL)23 axis, have been recently approved for psoriasis management. However, real-life data regarding their comparison are scant.The ...

3 March 2021 in Journal of the European Academy of Dermatology and Venereology
Verified
Journal Article
Closed access
PDF file
AVAlessia Villani
Alessia Villani
GFG. Fabbrocini
G. Fabbrocini
JOJ. Ocampo‐Candiani
J. Ocampo‐Candiani
ARAngelo Ruggiero
Angelo Ruggiero
Sonia Sofía Ocampo-GarzaSonia Sofía Ocampo-Garza
Sonia Sofía Ocampo-Garza

23 December 2021 in Journal of Personalized Medicine
Verified
Journal Article
Open access
PDF file
GGGianluca Gatta
Gianluca Gatta
GGGraziella Di Grezia
Graziella Di Grezia
Vincenzo CuccurulloVincenzo Cuccurullo
Vincenzo Cuccurullo
Celestino SarduCelestino Sardu
Celestino Sardu
FIFrancesco Iovino
Francesco Iovino
LVLuigi Viola
Luigi Viola
Magnetic resonance imaging (MRI) offers excellent spatial and contrast resolution for evaluating a wide variety of pathologies, without exposing patients to ionizing radiations. Additionally, MRI offers reproducible diagnostic imaging results that are not operator-dependent, a major advantage over ultrasound. MRI is commonly used in pregnant women to evaluate, most frequently, acute abdominal and pelvic pain or placental abnormalities, as well as neurological or fetal abnormalities, infections, or neoplasms. However, to date, our knowledge about MRI safety during pregnancy, especially about the administration of gadolinium-based contrast agents, which are able to cross the placental barrier, is still limited, raising concerns about possible negative effects on both the mother and the health of the fetus. Contrast agents that are unable to cross the placenta in a way that is safe for the fetus are desirable. In recent years, some preclinical studies, carried out in rodent models, have evaluated the role of long circulating liposomal nanoparticle-based blood-pool gadolinium contrast agents that do not penetrate the placental barrier due to their size and therefore do not expose the fetus to the contrast agent during pregnancy, preserving it from any hypothetical risks. Hence, we performed a literature review focusing on contrast and non-contrast MRI use during pregnancy.

16 August 2022 in Expert Opinion on Biological Therapy
Verified
Journal Article
Closed access
Elisa CamelaElisa Camela
Elisa Camela
LPLuca Potestio
Luca Potestio
Gabriella FabbrociniGabriella Fabbrocini
Gabriella Fabbrocini
ARAngelo Ruggiero
Angelo Ruggiero
MMMatteo Megna
Matteo Megna
Personalized medicine is the new frontier in psoriasis as it may allow a patient-tailored management with treatment optimization and reduction of side effects as well as health costs [1]. Thanks to...