Factors predictive of response, disease progression, and overall survival after dabrafenib and trametinib combination treatment: a pooled analysis of individual patient data from randomised trials.
Identifieur interne : 001F04 ( Main/Exploration ); précédent : 001F03; suivant : 001F05Factors predictive of response, disease progression, and overall survival after dabrafenib and trametinib combination treatment: a pooled analysis of individual patient data from randomised trials.
Auteurs : Georgina V. Long [Australie] ; Jean-Jacques Grob [France] ; Paul Nathan [Royaume-Uni] ; Antoni Ribas [États-Unis] ; Caroline Robert [France] ; Dirk Schadendorf [Allemagne] ; Stephen R. Lane [États-Unis] ; Carmen Mak [États-Unis] ; Philippe Legenne [Suisse] ; Keith T. Flaherty [États-Unis] ; Michael A. Davies [États-Unis]Source :
- The Lancet. Oncology [ 1474-5488 ] ; 2016.
Descripteurs français
- KwdFr :
- Essais contrôlés randomisés comme sujet, Femelle, Humains, Imidazoles (administration et posologie), Mutation, Mâle, Mélanome (génétique), Mélanome (mortalité), Mélanome (traitement médicamenteux), Oximes (administration et posologie), Protocoles de polychimiothérapie antinéoplasique (usage thérapeutique), Protéines proto-oncogènes B-raf (génétique), Pyridones (administration et posologie), Pyrimidinones (administration et posologie), Études rétrospectives, Évolution de la maladie.
- MESH :
- administration et posologie : Imidazoles, Oximes, Pyridones, Pyrimidinones.
- génétique : Mélanome, Protéines proto-oncogènes B-raf.
- mortalité : Mélanome.
- traitement médicamenteux : Mélanome.
- usage thérapeutique : Protocoles de polychimiothérapie antinéoplasique.
- Essais contrôlés randomisés comme sujet, Femelle, Humains, Mutation, Mâle, Études rétrospectives, Évolution de la maladie.
English descriptors
- KwdEn :
- Antineoplastic Combined Chemotherapy Protocols (therapeutic use), Disease Progression, Female, Humans, Imidazoles (administration & dosage), Male, Melanoma (drug therapy), Melanoma (genetics), Melanoma (mortality), Mutation, Oximes (administration & dosage), Proto-Oncogene Proteins B-raf (genetics), Pyridones (administration & dosage), Pyrimidinones (administration & dosage), Randomized Controlled Trials as Topic, Retrospective Studies.
- MESH :
- chemical , administration & dosage : Imidazoles, Oximes, Pyridones, Pyrimidinones.
- drug therapy : Melanoma.
- genetics : Melanoma, Proto-Oncogene Proteins B-raf.
- mortality : Melanoma.
- therapeutic use : Antineoplastic Combined Chemotherapy Protocols.
- Disease Progression, Female, Humans, Male, Mutation, Randomized Controlled Trials as Topic, Retrospective Studies.
Abstract
Dabrafenib plus trametinib treatment provides significant benefits over BRAF-inhibitor monotherapy in patients with BRAF(V600E)-mutant or BRAF(V600K)-mutant advanced melanoma; however, in many patients the disease progresses, leading to death. With many treatment options available, understanding clinical factors that predict long-term response and survival for treatments is important for optimisation of patient management. We aimed to identify clinical factors associated with long-term response and survival using pooled data from randomised trials of dabrafenib plus trametinib in patients with metastatic BRAF-mutant melanoma.
DOI: 10.1016/S1470-2045(16)30578-2
PubMed: 27864013
Affiliations:
- Allemagne, Australie, France, Royaume-Uni, Suisse, États-Unis
- Bade-Wurtemberg, Californie, District de Karlsruhe, Massachusetts, New Jersey, Nouvelle-Galles du Sud, Texas, Île-de-France
- Heidelberg, Orsay, Sydney
- Université Paris-Sud, Université de Sydney
Links toward previous steps (curation, corpus...)
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- to stream PubMed, to step Checkpoint: 001479
- to stream Ncbi, to step Merge: 003F02
- to stream Ncbi, to step Curation: 003F02
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Le document en format XML
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<front><div type="abstract" xml:lang="en">Dabrafenib plus trametinib treatment provides significant benefits over BRAF-inhibitor monotherapy in patients with BRAF(V600E)-mutant or BRAF(V600K)-mutant advanced melanoma; however, in many patients the disease progresses, leading to death. With many treatment options available, understanding clinical factors that predict long-term response and survival for treatments is important for optimisation of patient management. We aimed to identify clinical factors associated with long-term response and survival using pooled data from randomised trials of dabrafenib plus trametinib in patients with metastatic BRAF-mutant melanoma.</div>
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<country name="Royaume-Uni"><noRegion><name sortKey="Nathan, Paul" sort="Nathan, Paul" uniqKey="Nathan P" first="Paul" last="Nathan">Paul Nathan</name>
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<country name="États-Unis"><region name="Californie"><name sortKey="Ribas, Antoni" sort="Ribas, Antoni" uniqKey="Ribas A" first="Antoni" last="Ribas">Antoni Ribas</name>
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<name sortKey="Lane, Stephen R" sort="Lane, Stephen R" uniqKey="Lane S" first="Stephen R" last="Lane">Stephen R. Lane</name>
<name sortKey="Mak, Carmen" sort="Mak, Carmen" uniqKey="Mak C" first="Carmen" last="Mak">Carmen Mak</name>
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<country name="Allemagne"><region name="Bade-Wurtemberg"><name sortKey="Schadendorf, Dirk" sort="Schadendorf, Dirk" uniqKey="Schadendorf D" first="Dirk" last="Schadendorf">Dirk Schadendorf</name>
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<country name="Suisse"><noRegion><name sortKey="Legenne, Philippe" sort="Legenne, Philippe" uniqKey="Legenne P" first="Philippe" last="Legenne">Philippe Legenne</name>
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