Dovitinib versus sorafenib for third-line targeted treatment of patients with metastatic renal cell carcinoma: an open-label, randomised phase 3 trial.
Identifieur interne : 003A13 ( Main/Exploration ); précédent : 003A12; suivant : 003A14Dovitinib versus sorafenib for third-line targeted treatment of patients with metastatic renal cell carcinoma: an open-label, randomised phase 3 trial.
Auteurs : Robert J. Motzer [États-Unis] ; Camillo Porta [Italie] ; Nicholas J. Vogelzang [États-Unis] ; Cora N. Sternberg [Italie] ; Cezary Szczylik [Pologne] ; Jakub Zolnierek [Pologne] ; Christian Kollmannsberger [Canada] ; Sun Young Rha [Corée du Sud] ; Georg A. Bjarnason [Canada] ; Bohuslav Melichar [République tchèque] ; Ugo De Giorgi [Italie] ; Viktor Grünwald [Allemagne] ; Ian D. Davis [Australie] ; Jae-Lyun Lee [Corée du Sud] ; Emilio Esteban [Espagne] ; Gladys Urbanowitz [États-Unis] ; Can Cai [États-Unis] ; Matthew Squires [Suisse] ; Mahtab Marker [États-Unis] ; Michael M. Shi [États-Unis] ; Bernard Escudier [France]Source :
- The Lancet. Oncology [ 1474-5488 ] ; 2014.
Descripteurs français
- KwdFr :
- Adolescent, Adulte, Adulte d'âge moyen, Antinéoplasiques (usage thérapeutique), Benzimidazoles (effets indésirables), Benzimidazoles (usage thérapeutique), Facteur de croissance endothéliale vasculaire de type A (antagonistes et inhibiteurs), Femelle, Humains, Inhibiteurs de protéines kinases (usage thérapeutique), Mâle, Métastase tumorale, Nicotinamide (analogues et dérivés), Nicotinamide (effets indésirables), Nicotinamide (usage thérapeutique), Néphrocarcinome (mortalité), Néphrocarcinome (secondaire), Néphrocarcinome (traitement médicamenteux), Phénylurées (effets indésirables), Phénylurées (usage thérapeutique), Quinolinone (effets indésirables), Quinolinone (usage thérapeutique), Sujet âgé, Sujet âgé de 80 ans ou plus, Tumeurs du rein (mortalité), Tumeurs du rein (traitement médicamenteux).
- MESH :
- analogues et dérivés : Nicotinamide.
- antagonistes et inhibiteurs : Facteur de croissance endothéliale vasculaire de type A.
- effets indésirables : Benzimidazoles, Nicotinamide, Phénylurées, Quinolinone.
- mortalité : Néphrocarcinome, Tumeurs du rein.
- secondaire : Néphrocarcinome.
- traitement médicamenteux : Néphrocarcinome, Tumeurs du rein.
- usage thérapeutique : Antinéoplasiques, Benzimidazoles, Inhibiteurs de protéines kinases, Nicotinamide, Phénylurées, Quinolinone.
- Adolescent, Adulte, Adulte d'âge moyen, Femelle, Humains, Mâle, Métastase tumorale, Sujet âgé, Sujet âgé de 80 ans ou plus.
English descriptors
- KwdEn :
- Adolescent, Adult, Aged, Aged, 80 and over, Antineoplastic Agents (therapeutic use), Benzimidazoles (adverse effects), Benzimidazoles (therapeutic use), Carcinoma, Renal Cell (drug therapy), Carcinoma, Renal Cell (mortality), Carcinoma, Renal Cell (secondary), Female, Humans, Kidney Neoplasms (drug therapy), Kidney Neoplasms (mortality), Male, Middle Aged, Neoplasm Metastasis, Niacinamide (adverse effects), Niacinamide (analogs & derivatives), Niacinamide (therapeutic use), Phenylurea Compounds (adverse effects), Phenylurea Compounds (therapeutic use), Protein Kinase Inhibitors (therapeutic use), Quinolones (adverse effects), Quinolones (therapeutic use), Vascular Endothelial Growth Factor A (antagonists & inhibitors).
- MESH :
- chemical , adverse effects : Benzimidazoles, Niacinamide, Phenylurea Compounds, Quinolones.
- chemical , analogs & derivatives : Niacinamide.
- chemical , antagonists & inhibitors : Vascular Endothelial Growth Factor A.
- chemical , therapeutic use : Antineoplastic Agents, Benzimidazoles, Niacinamide, Phenylurea Compounds, Protein Kinase Inhibitors, Quinolones.
- drug therapy : Carcinoma, Renal Cell, Kidney Neoplasms.
- mortality : Carcinoma, Renal Cell, Kidney Neoplasms.
- secondary : Carcinoma, Renal Cell.
- Adolescent, Adult, Aged, Aged, 80 and over, Female, Humans, Male, Middle Aged, Neoplasm Metastasis.
Abstract
An unmet medical need exists for patients with metastatic renal cell carcinoma who have progressed on VEGF-targeted and mTOR-inhibitor therapies. Fibroblast growth factor (FGF) pathway activation has been proposed as a mechanism of escape from VEGF-targeted therapies. Dovitinib is an oral tyrosine-kinase inhibitor that inhibits VEGF and FGF receptors. We therefore compared dovitinib with sorafenib as third-line targeted therapies in patients with metastatic renal cell carcinoma.
DOI: 10.1016/S1470-2045(14)70030-0
PubMed: 24556040
Affiliations:
- Allemagne, Australie, Canada, Corée du Sud, Espagne, France, Italie, Pologne, République tchèque, Suisse, États-Unis
- Latium, Nevada, New Jersey, Région capitale de Séoul, État de New York
- Rome, Séoul
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: 003913
- to stream PubMed, to step Curation: 003798
- to stream PubMed, to step Checkpoint: 003798
- to stream Ncbi, to step Merge: 001801
- to stream Ncbi, to step Curation: 001801
- to stream Ncbi, to step Checkpoint: 001801
- to stream Main, to step Merge: 003A56
- to stream Main, to step Curation: 003A13
Le document en format XML
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<author><name sortKey="Shi, Michael M" sort="Shi, Michael M" uniqKey="Shi M" first="Michael M" last="Shi">Michael M. Shi</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Dovitinib versus sorafenib for third-line targeted treatment of patients with metastatic renal cell carcinoma: an open-label, randomised phase 3 trial.</title>
<author><name sortKey="Motzer, Robert J" sort="Motzer, Robert J" uniqKey="Motzer R" first="Robert J" last="Motzer">Robert J. Motzer</name>
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<author><name sortKey="Porta, Camillo" sort="Porta, Camillo" uniqKey="Porta C" first="Camillo" last="Porta">Camillo Porta</name>
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<author><name sortKey="Vogelzang, Nicholas J" sort="Vogelzang, Nicholas J" uniqKey="Vogelzang N" first="Nicholas J" last="Vogelzang">Nicholas J. Vogelzang</name>
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<author><name sortKey="Sternberg, Cora N" sort="Sternberg, Cora N" uniqKey="Sternberg C" first="Cora N" last="Sternberg">Cora N. Sternberg</name>
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<author><name sortKey="Szczylik, Cezary" sort="Szczylik, Cezary" uniqKey="Szczylik C" first="Cezary" last="Szczylik">Cezary Szczylik</name>
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<author><name sortKey="Zolnierek, Jakub" sort="Zolnierek, Jakub" uniqKey="Zolnierek J" first="Jakub" last="Zolnierek">Jakub Zolnierek</name>
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<author><name sortKey="Kollmannsberger, Christian" sort="Kollmannsberger, Christian" uniqKey="Kollmannsberger C" first="Christian" last="Kollmannsberger">Christian Kollmannsberger</name>
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<author><name sortKey="Rha, Sun Young" sort="Rha, Sun Young" uniqKey="Rha S" first="Sun Young" last="Rha">Sun Young Rha</name>
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<wicri:regionArea>Yonsei Cancer Center, Yonsei University College of Medicine, Seoul</wicri:regionArea>
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</placeName>
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<author><name sortKey="Bjarnason, Georg A" sort="Bjarnason, Georg A" uniqKey="Bjarnason G" first="Georg A" last="Bjarnason">Georg A. Bjarnason</name>
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<author><name sortKey="Melichar, Bohuslav" sort="Melichar, Bohuslav" uniqKey="Melichar B" first="Bohuslav" last="Melichar">Bohuslav Melichar</name>
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<author><name sortKey="De Giorgi, Ugo" sort="De Giorgi, Ugo" uniqKey="De Giorgi U" first="Ugo" last="De Giorgi">Ugo De Giorgi</name>
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<author><name sortKey="Grunwald, Viktor" sort="Grunwald, Viktor" uniqKey="Grunwald V" first="Viktor" last="Grünwald">Viktor Grünwald</name>
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<author><name sortKey="Davis, Ian D" sort="Davis, Ian D" uniqKey="Davis I" first="Ian D" last="Davis">Ian D. Davis</name>
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<affiliation wicri:level="1"><nlm:affiliation>Hospital Universitario Central de Asturias, Oviedo, Asturias, Spain.</nlm:affiliation>
<country xml:lang="fr">Espagne</country>
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</author>
<author><name sortKey="Urbanowitz, Gladys" sort="Urbanowitz, Gladys" uniqKey="Urbanowitz G" first="Gladys" last="Urbanowitz">Gladys Urbanowitz</name>
<affiliation wicri:level="2"><nlm:affiliation>Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
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<placeName><region type="state">New Jersey</region>
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<author><name sortKey="Squires, Matthew" sort="Squires, Matthew" uniqKey="Squires M" first="Matthew" last="Squires">Matthew Squires</name>
<affiliation wicri:level="1"><nlm:affiliation>Novartis Pharma, Basel, Switzerland.</nlm:affiliation>
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<wicri:regionArea>Novartis Pharma, Basel</wicri:regionArea>
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<country xml:lang="fr">États-Unis</country>
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<author><name sortKey="Shi, Michael M" sort="Shi, Michael M" uniqKey="Shi M" first="Michael M" last="Shi">Michael M. Shi</name>
<affiliation wicri:level="2"><nlm:affiliation>Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.</nlm:affiliation>
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<series><title level="j">The Lancet. Oncology</title>
<idno type="eISSN">1474-5488</idno>
<imprint><date when="2014" type="published">2014</date>
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<front><div type="abstract" xml:lang="en">An unmet medical need exists for patients with metastatic renal cell carcinoma who have progressed on VEGF-targeted and mTOR-inhibitor therapies. Fibroblast growth factor (FGF) pathway activation has been proposed as a mechanism of escape from VEGF-targeted therapies. Dovitinib is an oral tyrosine-kinase inhibitor that inhibits VEGF and FGF receptors. We therefore compared dovitinib with sorafenib as third-line targeted therapies in patients with metastatic renal cell carcinoma.</div>
</front>
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