نتایج جستجو برای: vemurafenib

تعداد نتایج: 1054  

2017
Antonio M Grimaldi Ester Simeone Lucia Festino Vito Vanella Paolo A Ascierto

A cquired resistance is the most common cause of BRAF inhibitor monotherapy treatment failure, with the majority of patients experiencing disease progression with a median progression-free survival of 6-8 months. As such, there has been considerable focus on combined therapy with dual BRAF and MEK inhibition as a means to improve outcomes compared with monotherapy. In the COMBI-d and COMBI-v tr...

Journal: :Lab on a chip 2015
Dipali Patel Yandong Gao Kyungjin Son Christian Siltanen Richard M Neve Katherine Ferrara Alexander Revzin

Targeted cancer therapies are designed to deactivate signaling pathways used by cancer cells for survival. However, cancer cells are often able to adapt by activating alternative survival pathways, thereby acquiring drug resistance. An emerging theory is that autocrine or paracrine growth factor signaling in the cancer microenvironment represent an important mechanism of drug resistance. In the...

Journal: :The Journal of pharmacology and experimental therapeutics 2012
Rajendar K Mittapalli Shruthi Vaidhyanathan Ramola Sane William F Elmquist

Vemurafenib [N-(3-{[5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]carbonyl}-2,4-difluorophenyl)propane-1-sulfonamide(PLX4032)] is a novel small-molecule BRAF inhibitor, recently approved by the Food and Drug Administration for the treatment of patients with metastatic melanoma with a BRAF(V600E) mutation. The objective of this study was to investigate the role of P-glycoprotein (P-gp) and br...

2015
Heidrun Mitzel Stephan Grabbe Carmen Loquai

INTRODUCTION Vemurafenib has been approved since 2011 in the United States for the treatment of advanced BRAF V600emutated melanoma as first-line therapy. Although it significantly prolongs overall and progression-free survival, most patients relapse within 6 to 8 months owing to acquisition of drug resistance. New findings suggest that discontinuous dose administration of vemurafenib might pro...

Journal: :Cancer journal 2014
Lawrence Flaherty Omid Hamid Gerald Linette Lynn Schuchter Sigrun Hallmeyer Rene Gonzalez C Lance Cowey Anna Pavlick Fred Kudrik Brendan Curti David Lawson Paul B Chapman Kim Margolin Antoni Ribas David McDermott Keith Flaherty Lee Cranmer F Stephen Hodi Bann-Mo Day Rolf Linke John Hainsworth

PURPOSE This open-label, multicenter study was designed to allow access to vemurafenib for patients with metastatic melanoma, bridging the time between end of enrollment in the phase III registration trial (December 2010) and commercial availability following US Food and Drug Administration approval of vemurafenib for the treatment of unresectable or metastatic BRAF-mutated melanoma (August 201...

2016
Casey Quinn Qiufei Ma Amber Kudlac Stephen Palmer Beth Barber Zhongyun Zhao

INTRODUCTION Few randomized controlled trials have compared new treatments for metastatic melanoma. We sought to examine the relative treatment effect of talimogene laherparepvec compared with ipilimumab and vemurafenib. METHODS A systematic literature review of treatments for metastatic melanoma was undertaken but a valid network of evidence could not be established because of a lack of comp...

2012
Andreas R Baudy Taner Dogan Judith E Flores-Mercado Klaus P Hoeflich Fei Su Nicholas van Bruggen Simon-Peter Williams

BACKGROUND The BRAF inhibitor, vemurafenib, has recently been approved for the treatment of metastatic melanoma in patients harboring BRAFV600 mutations. Currently, dual BRAF and MEK inhibition are ongoing in clinical trials with the goal of overcoming the acquired resistance that has unfortunately developed in some vemurafenib patients. FDG-PET measures of metabolic activity are increasingly e...

2015
DANIELA PUCCIARELLI NINA LENGGER MARTINA TAKACOVA LUCIA CSADEROVA MARIA BARTOSOVA HEIMO BREITENEDER SILVIA PASTOREKOVA CHRISTINE HAFNER

Chondroitin sulfate proteoglycan 4 (CSPG4), a highly immunogenic melanoma tumor antigen, is a potential target for antibody-based immunotherapy. The mechanism by which CSPG4 affects melanoma progression is only partly understood, in particular the involvement of other receptor tyrosine kinases and the tumor microenvironment. We have previously reported on a mimotope-based vaccine against CSPG4 ...

2016
Lindsay C. Spender G. John Ferguson Sijia Liu Chao Cui Maria Romina Girotti Gary Sibbet Ellen B. Higgs Morven K. Shuttleworth Tom Hamilton Paul Lorigan Michael Weller David F. Vincent Owen J. Sansom Margaret Frame Peter ten Dijke Richard Marais Gareth J. Inman

Recent data implicate elevated transforming growth factor-β (TGFβ) signalling in BRAF inhibitor drug-resistance mechanisms, but the potential for targeting TGFβ signalling in cases of advanced melanoma has not been investigated. We show that mutant BRAFV600E confers an intrinsic dependence on TGFβ/TGFβ receptor 1 (TGFBR1) signalling for clonogenicity of murine melanocytes. Pharmacological inhib...

2012
Rosalie Fisher James Larkin

The BRAF inhibitor, vemurafenib, has demonstrated improved progression-free and overall survival compared with chemotherapy in a randomized trial, and represents a new standard of care in patients with advanced melanoma harboring a BRAF-V600 mutation. A BRAF-V600 mutation is identified in approximately half of patients with cutaneous melanoma, and is unequivocally a biomarker predictive of prof...

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