Results 161 to 170 of about 82,604 (202)
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Ophthalmic adverse effects of BRAF inhibitors

European Journal of Ophthalmology, 2022
To determine the frequency, characteristics, and clinical course of ophthalmic side effects associated with systemic BRAF inhibitor therapy. Medical records of patients taking BRAF inhibitors for the treatment of systemic malignances at Mayo Clinic, Rochester from 01/01/2010 to 08/30/2021, were retrospectively reviewed.
Clara M. Castillejo Becerra   +2 more
openaire   +2 more sources

BRAF inhibitor therapy in HCL

Best Practice & Research Clinical Haematology, 2015
Targeted treatment approaches are transforming the therapeutic landscape of cancer care. The discovery of the BRAF V600E mutation in most cases of classical hairy cell leukemia opens up unique opportunities for tumor specific treatment of HCL targeting the MEK/ERK signaling pathway.
Sascha, Dietrich, Thorsten, Zenz
openaire   +2 more sources

Emerging BRAF inhibitors for melanoma

Expert Opinion on Emerging Drugs, 2013
The clinical activity of BRAF inhibitor (BRAF-I) therapy is a major breakthrough in the treatment of metastatic melanoma carrying BRAF mutations. However, the therapeutic efficacy of BRAF-I therapy is limited due to the onset of intrinsic and acquired drug resistance.The role of wild-type BRAF in melanocytes and of the mutated BRAF in the pathogenesis ...
Sabbatino, Francesco   +4 more
openaire   +2 more sources

BRAF inhibitors in cancer therapy

Pharmacology & Therapeutics, 2014
Activating BRAF mutations, leading to constitutive activation of the MAPK signaling pathway, are common in a variety of human cancers. Several small molecule BRAF inhibitors have been developed during the last years and shown promising results in clinical trials, especially for metastatic melanoma, while they have been less effective in colon cancer ...
Carolina, Hertzman Johansson   +1 more
openaire   +2 more sources

BRAF Inhibitors and Melanoma

The Cancer Journal, 2011
Selective BRAF inhibitors have recently emerged as a new standard treatment for patients with metastatic melanoma harboring activating BRAF mutations. Inhibition of the MAP kinase pathway and initial evidence of antitumor effects are very reliably observed. However, many patients experience short-lived responses, whereas others are durable.
openaire   +2 more sources

Overcoming metastatic melanoma with BRAF inhibitors

Archives of Pharmacal Research, 2011
Melanoma has the capacity to spread via the blood stream to the brain, and has been notoriously resistant to drug therapy. An activating mutation in the gene encoding BRAF is known to be responsible for half of melanomas. This article provides a review of GSK2118436 and PLX4032 as potential therapeutics for the treatment of melanomas by inhibiting ...
Seunghee, Hong   +2 more
openaire   +2 more sources

BRAF inhibitors in BRAF-V600 mutated primary neuroepithelial brain tumors

Expert Opinion on Investigational Drugs, 2015
Primary neuroepithelial brain tumors encompass a wide variety of glial and glioneuronal neoplasms. Malignant tumors, tumors located in surgically inaccessible locations (e.g., eloquent brain areas, deep structures, brain stem) and recurrent or progressive tumors pose considerable treatment challenges and are candidates for novel therapeutics based on ...
Matthias, Preusser   +2 more
openaire   +2 more sources

Actin’ against BRAF inhibitors

Science Signaling, 2016
Blocking actin polymerization prevents YAP and TAZ activation and resistance to BRAF inhibitors in melanoma.
openaire   +1 more source

BRAF and MEK inhibitors in BRAF-mutant melanoma

The Lancet Oncology, 2012
Patients with melanoma and the Val600 BRAF mutation benefi t from combined inhibition of BRAF and MEK, according to a new study. Selective BRAF inhibitors such as dabrafenib and MEK inhibitors such as trametinib have individually been shown to increase progressionfree survival (PFS) and overall survival in Val600 BRAF-mutant melanoma.
openaire   +1 more source

BRAF inhibitor rechallenge in patients with advanced BRAF V600-mutant melanoma

Melanoma Research, 2015
In around 50% of melanomas, the BRAF V600 mutation, resulting in an activation of the MAP kinase pathway, is detected. BRAF inhibitors have shown remarkable activity on the disease. However, efficacy is short-lived in most cases, with a median disease-free survival of 6 months.
Jennifer, Roux   +12 more
openaire   +2 more sources

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