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Objectives Metastasis of multiple regional lymph nodes and extracapsular spread in the metastatic nodes are found to be negative prognostic factors for oral squamous cell carcinomas (OSCCs), and many studies on the prediction of nodal metastasis according to the clinicopathologic and cellular/molecular features of cancer cells have been conducted.
Annals of Oncology 12/14/2019 19:00
Abstract. Background. Corticosteroids (CS) are often prescribed for patients (pts) with cancer to alleviate disease symptoms, manage treatment-related adverse events, or treat underlying comorbidities. Immunosuppressive properties of CS may impact the effectiveness of cancer immunotherapy (CIT) if given concomitantly. This study explored the association of baseline CS use with outcomes in CIT-treated pts with advanced melanoma (aMel), advanced non-small cell lung cancer (aNSCLC) or advanced urothelial cancer (aUC). Methods. Retrospective observational study of pts in the Flatiron Health de-identified electronic health record–derived database diagnosed Jan 2011-Jun 2017 with aMel, aNSCLC or aUC and treated with CIT only in any line. Baseline CS.
Annals of Oncology 12/14/2019 19:00
Abstract. Background. VCN-01 is an oncolytic adenovirus with replication restricted to cells with a nonfunctional retinoblastoma pathway. Upon selective replication VCN-01 expresses the matrix remodeling-enzyme hyaluronidase to enhance virus spreading and tumor uptake of different therapeutics, including immune check-point inhibitors. In a phase I performed in pancreatic carcinoma VCN-01 reached tumors after systemic administration and induced CD8-infiltration, tumor inflammation and PD-1/PD-L1 up-regulation. We hypothesize these intratumor effects may help to overcome the observed resistance to Durvalumab and other PD-(L)-1 checkpoint inhibitors. Trial Design. NCT03799744 is a multi-center, open-label dose-escalation phase I study evaluating t.
Onclive 12/13/2019 13:22
... The triplet regimen of atezolizumab (Tecentriq), cobimetinib (Cotellic), and vemurafenib (Zelboraf) was found to improve progression-free survival (PFS) compared with cobimetinib/vemurafenib plus placebo in patients with previously untreated BRAF V600 mutation–positive advanced melanoma, meeting the primary endpoint of the phase III IMspire150 study (NCT02908672.
Targeted Oncology 12/13/2019 11:43
The combination of atezolizumab (Zelboraf), cobimetinib (Cotellic), and vemurafenib (Zelboraf) reduced the risk of disease progression or death compared with placebo in patients with BRAF V600 mutation-positive advanced melanoma, meeting the primary endpoint of progression-free survival (PFS) in the phase III IMspire150 study (NCT02908672), according to a press release from Roche. 12/13/2019 06:57
Condition : Head and Neck Squamous Cell Carcinoma Interventions : Drug: Lenvatinib; Drug: Pembrolizumab; Drug: Placebo Sponsor : Merck Sharp & Dohme Corp. Not yet recruiting.
Molecular characterization of lung squamous cell carcinoma (LUSC), one of the major subtypes of lung cancer, has not sufficiently improved its nonstratified treatment strategies over decades. Accumulating evidence suggests that lineage-specific transcriptional regulators control differentiation states during cancer evolution and underlie their distinct biological behaviors. In this study, by investigating the super-enhancer landscape of LUSC, we identified a previously undescribed “neural” subtype defined by Sox2 and a neural lineage factor Brn2, as well as the classical LUSC subtype defined by Sox2 and its classical squamous partner p63. Robust protein–protein interaction and genomic cooccupancy of Sox2 and Brn2, in place for p63 in the cl.
Purpose:. The identification of high-risk patients within human papillomavirus (HPV)-positive and -negative head and neck squamous cell carcinoma (HNSCC) is needed for improved treatment and surveillance strategies. In this study, we set out to discover antibody responses (AR) with prognostic impact in HNSCC stratified by HPV status. Experimental Design:. A fluorescent bead–based multiplex serology assay on 29 cancer antigens (16 cancer-testis antigens, 5 cancer-retina antigens, and 8 oncogenes) and 29 HPV antigens was performed in samples of 362 patients with HNSCC from five independent cohorts (153 HPV positive, 209 HPV negative). A multivariable Cox proportional hazard model with bootstrapping (M = 1000) was used for validation of prognost.

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