Antonio Russo

Prof. Antonio Russo

Department of Surgical, Oncological and Oral Sciences, University of Palermo, 90127 Palermo, Italy
orcid

Research Focus & Metrics

Academic Career Length

36Years (1991-Present)

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

Representative Publications

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31 July 2003 in Journal of Cellular Physiology
Verified
Journal Article
Closed access
PDF file
VCValentina Calò
Valentina Calò
MMManuela Migliavacca
Manuela Migliavacca
VBViviana Bazan
Viviana Bazan
MMMarcella Macaluso
Marcella Macaluso
MBMaria Buscemi
Maria Buscemi
Antonio RussoAntonio Russo
Antonio Russo

1 September 2019 in Cellular Immunology
Verified
Journal Article
Closed access
GBGiuseppe Badalamenti
Giuseppe Badalamenti
DFDaniele Fanale
Daniele Fanale
LILorena Incorvaia
Lorena Incorvaia
NBNadia Barraco
Nadia Barraco
ALAngela Listì
Angela Listì
Antonio RussoAntonio Russo
Antonio Russo

5 March 2012 in Annals of Oncology
Verified
Journal Article
Open access
PDF file
SDSantini Daniele
Santini Daniele
BVBruno Vincenzi
Bruno Vincenzi
RARaffale Addeo
Raffale Addeo
CGC. Garufi
C. Garufi
Gianluca MasiGianluca Masi
Gianluca Masi
GTG. Tonini
G. Tonini
Scientific data provide the evidence that secondary K-RAS mutations do not occur during anti-epidermal growth factor receptor therapy in colorectal cancer patients. This multicenter phase II prospective study aims to investigate the activity of a retreatment with a cetuximab-based therapy. We enrolled 39 irinotecan-refractory patients who had a clinical benefit after a line of cetuximab- plus irinotecan-based therapy and then a progression of disease for which underwent a new line chemotherapy and finally, after a clear new progression of disease, were retreated with the same cetuximab- plus irinotecan-based therapy. Median number of therapeutic lines before accrual was 4. Median interval time between last cycle of first cetuximab-based therapy and first cycle of the retreatment was 6 months. Overall response rate was 53.8% with 19 partial responses (48.7%) and 2 complete responses (5.1%). Disease stabilization was obtained in 35.9% of patients and progression in four patients (10.2%). Median progression-free survival was 6.6 months. The correlation between skin toxicity during first cetuximab therapy and during cetuximab rechallenge was significant (P = 0.01). Rechallenge with the same cetuximab-based therapy may achieve a new important clinical benefit further delaying the progression of disease and improving the therapeutic options.

28 September 2018
Verified
Book Chapter
Closed access
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DFDaniele Fanale
Daniele Fanale
STSimona Taverna
Simona Taverna
Antonio RussoAntonio Russo
Antonio Russo
VBViviana Bazan
Viviana Bazan

1 November 2019 in Critical Reviews in Oncology/Hematology
Verified
Journal Article
Closed access
SGStefania Gori
Stefania Gori
AIAlessandro Inno
Alessandro Inno
LBLorenzo Belluomini
Lorenzo Belluomini
PBPaolo Bocus
Paolo Bocus
ZBZeno Bisoffi
Zeno Bisoffi
GAGuido Arcaro
Guido Arcaro

22 February 2016 in Oncotarget
Verified
Journal Article
Open access
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FPFrancesco Passiglia
Francesco Passiglia
GBGiuseppe Bronte
Giuseppe Bronte
VBViviana Bazan
Viviana Bazan
CNClara Natoli
Clara Natoli
SRSergio Rizzo
Sergio Rizzo
Antonio RussoAntonio Russo
Antonio Russo
PD-L1 expression as predictive biomarker in patients with NSCLC: a pooled analysis PD-L1 expression as predictive biomarker in patients with NSCLC: a pooled analysis