Volume 12 Supplement 1
Melanoma Bridge 2013: Poster and Oral Presentations
Meeting abstracts
Edited by Paolo A Ascierto, Nicola Mozzillo, Francesco M Marincola, Gennaro Cilberto, John M Kirkwood, Giuseppe Masucci, Ignacio Melero, Antoni Ribas and Magdalena Thurin
The conference and publication charges for this supplement were funded by 3P Solution. Abstracts were selected by the Scientific Committee of the conference. Supplement Editor declarations: Ignacio Melero has served as a consultant and/or advisory board member for Bristol-Myers Squibb, Merck Serono and Genentech-Roche. John M Kirkwood has been a consultant for Bristol-Myers Squibb, Merck, GlaxoSmithKline, Novartis, Ziopharm, Celgene and Vical in the past five years. Paolo Ascierto has been a consultant for Bristol-Myers Squibb, Merck Sharp & Dohme, Roche-Genentech, GlaxoSmithKline, Ventana and Novartis. He has received research funds from Bristol-Myers Squibb, Roche-Genentech and Ventana. He has also received honoraria from Bristol-Myers Squibb, Roche-Genentech and GlaxoSmithKline. Antoni Ribas has been a consultant for Amgen, GlaxoSmithKline, Genentech-Roche, Merck, Novartis and Daiichi-Sanko with the honoraria paid to University of California, Los Angeles. He is also a stock holder in Kite Pharma and Flexus Biotherapeutics. Nicola Mozzillo, Francesco M Marincola, Gennaro Cilberto, Giuseppe Masucci and Magdalena Thurin declare that they have no competing interests.
Melanoma Bridge meeting 2013. Go to conference site.
Naples, Italy5-8 December 2013
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Citation: Journal of Translational Medicine 2014 12(Suppl 1):O1
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Activation of the ErbB3-AKT axis promotes melanoma cell survival and proliferation in response to RAF/MEK inhibition
Citation: Journal of Translational Medicine 2014 12(Suppl 1):O2 -
Assessment of germline and somatic alterations in main candidate genes among patients with multiple primary melanoma
Citation: Journal of Translational Medicine 2014 12(Suppl 1):O3 -
Regulation of melanoma initiating cells by Hedgehog signaling and SOX2
Citation: Journal of Translational Medicine 2014 12(Suppl 1):O4 -
Efficacy of radiotherapy in patients on progression after treatment with ipilimumab 3 mg/kg
Citation: Journal of Translational Medicine 2014 12(Suppl 1):O6 -
Updated results and correlative FDG-PET analysis of a phase IB study of vemurafenib and cobimetinib (MEK inhibitor [GDC-0973]), in advanced BRAF V600 - mutated melanoma (BRIM7)
Citation: Journal of Translational Medicine 2014 12(Suppl 1):O7 -
Peripheral and tumor immune correlates in patients with advanced melanoma treated with nivolumab (anti-PD-1, BMS-936558, ONO-4538) monotherapy or in combination with ipilimumab
Citation: Journal of Translational Medicine 2014 12(Suppl 1):O8 -
Ipilimumab treatment results in an early decrease in the frequency of circulating granulocytic myeloid derived suppressor cells as well as their arginase 1 production
Citation: Journal of Translational Medicine 2014 12(Suppl 1):O9 -
Harnessing host innate immunity may combat acquired resistance to BRAFi
Citation: Journal of Translational Medicine 2014 12(Suppl 1):O10 -
Regulated intratumoral expression of IL-12 as a basis for combination therapy in melanoma
Citation: Journal of Translational Medicine 2014 12(Suppl 1):O11 -
Biomarker analysis of on-treatment and at progression biopsies from BRIM7 - a phase 1B trial of combined vemurafenib and cobimetinib treatment in BRAF V600 mutated melanoma
Citation: Journal of Translational Medicine 2014 12(Suppl 1):O12 -
Systems biology analysis of immune signaling in peripheral blood mononuclear cells (PBMC) of melanoma patients receiving ipilimumab; basis for response biomarker identification
Citation: Journal of Translational Medicine 2014 12(Suppl 1):O13 -
Long-term response after electrochemotherapy in patients with relapsed or refractory cutaneous melanoma
Citation: Journal of Translational Medicine 2014 12(Suppl 1):P1 -
A novel approach to target metastases of melanoma cells in an organ-selective manner
Citation: Journal of Translational Medicine 2014 12(Suppl 1):P2 -
UV exposure and melanoma prognostic factors : results from Clinical National Melanoma Registry (CNMR)
Citation: Journal of Translational Medicine 2014 12(Suppl 1):P3 -
Psychological features in lower risk melanoma: an analysis on 204 patients
Citation: Journal of Translational Medicine 2014 12(Suppl 1):P4 -
Phase Ib/II, open-label, dose-escalation study of LGX818, an oral selective BRAF inhibitor, in combination with MEK162, an oral MEK1/2 inhibitor, in patients with BRAF V600-dependent advanced solid tumors: preliminary results
Citation: Journal of Translational Medicine 2014 12(Suppl 1):P5 -
Enrichment of KIR+CD57+ highly cytotoxic NK cells in sentinel lymph nodes of melanoma patients
Citation: Journal of Translational Medicine 2014 12(Suppl 1):P10 -
MISIPI study: Melanoma ImmunoScore evaluation in patients treated with IPIlimumab
Citation: Journal of Translational Medicine 2014 12(Suppl 1):P11 -
hMENA splicing program impacts the clinical outcome of early stage lung cancer patients. How and why?
Citation: Journal of Translational Medicine 2014 12(Suppl 1):P12 -
Natural immunomodulator preimplantation factor PIF affected cancer growth in malignant melanomas
Citation: Journal of Translational Medicine 2014 12(Suppl 1):P13 -
Combination therapy with ipilimumab and electrochemotherapy: preliminary efficacy results and correlation with immunological parameters
Citation: Journal of Translational Medicine 2014 12(Suppl 1):O5 -
In vivo targeting of cutaneous melanoma using an MSH-engineered human protein cage bearing fluorophore and MRI tracers
Citation: Journal of Translational Medicine 2014 12(Suppl 1):P6 -
Barasertib: a novel approach for the treatment of metastatic melanoma
Citation: Journal of Translational Medicine 2014 12(Suppl 1):P7 -
Overall survival of patients with chemotherapy-naive advanced melanoma treated with ipilimumab 3 mg/kg in clinical trials
Citation: Journal of Translational Medicine 2014 12(Suppl 1):P8 -
The mitochondrial master regulator gene PGC1alpha in novel sporadic melanoma cell lines: correlations with BRAF mutational status
Citation: Journal of Translational Medicine 2014 12(Suppl 1):P9
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