Serveur d'exploration sur les relations entre la France et l'Australie

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A phase II study of enzastaurin, a protein kinase C beta inhibitor, in patients with relapsed or refractory mantle cell lymphoma

Identifieur interne : 008703 ( Main/Curation ); précédent : 008702; suivant : 008704

A phase II study of enzastaurin, a protein kinase C beta inhibitor, in patients with relapsed or refractory mantle cell lymphoma

Auteurs : F. Morschhauser [France] ; J. F. Seymour [Australie] ; H. C. Kluin-Nelemans [Pays-Bas] ; A. Grigg [Australie] ; M. Wolf ; M. Pfreundschuh [Allemagne] ; H. Tilly [France] ; J. Raemaekers [Pays-Bas] ; M. B. Van T Veer [Pays-Bas] ; N. Milpied ; G. Cartron [France] ; A. Pezzutto [Allemagne] ; A. Spencer [Australie] ; F. Reyes [France] ; M. Dreyling [Allemagne]

Source :

RBID : ISTEX:38B1B9912C70FF2C6A99072E533CCF5D51222535

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English descriptors

Abstract

Background: Protein kinase C beta (PKCβ), a pivotal enzyme in B-cell signaling and survival, is overexpressed in most cases of mantle cell lymphoma (MCL). Activation of PI3K/AKT pathway is involved in pathogenesis of MCL. Enzastaurin, an oral serine/threonine kinase inhibitor, suppresses signaling through PKCβ/PI3K/AKT pathways, induces apoptosis, reduces proliferation, and suppresses tumor-induced angiogenesis. Patients and methods: Patients with relapsed/refractory MCL, and no more than four regimens of prior therapy, received 500 mg enzastaurin, orally, once daily. Results: Sixty patients, median age 66 years (range 45–85), Eastern Cooperative Oncology Group performance status of zero to two (48% had baseline International Prognostic Index of 3–5), were enrolled. Most patients had prior CHOP-like chemotherapy and/or rituximab (median = 2 regimens). No drug-related deaths occurred. There was one case each of grade 3 anemia, diarrhea, dyspnea, vomiting, hypotension, and syncope. Fatigue was the most common toxicity. Although no objective tumor responses occurred, 22 patients (37%, 95% CI 25% to 49%) were free from progression (FFP) for ≥3 cycles (one cycle = 28 days); 6 of 22 were FFP for >6 months. Two patients remain on treatment and FFP at >23 months. Conclusion: Freedom from progression for >6 months in six patients and a favorable toxicity profile with minimal hematological toxicity indicate that enzastaurin warrants evaluation as maintenance therapy and combination chemotherapy in MCL.

Url:
DOI: 10.1093/annonc/mdm463

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ISTEX:38B1B9912C70FF2C6A99072E533CCF5D51222535

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F. Morschhauser
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M. Wolf
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N. Milpied
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Le document en format XML

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<term>B cell neoplasm</term>
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<term>Enzastaurin</term>
<term>Human</term>
<term>Inhibitor</term>
<term>Mantle cell lymphoma</term>
<term>Phase II trial</term>
<term>Protein kinase C</term>
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<term>Enzastaurine</term>
<term>Essai clinique phase II</term>
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<term>Hémopathie lymphoïde B</term>
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<div type="abstract">Background: Protein kinase C beta (PKCβ), a pivotal enzyme in B-cell signaling and survival, is overexpressed in most cases of mantle cell lymphoma (MCL). Activation of PI3K/AKT pathway is involved in pathogenesis of MCL. Enzastaurin, an oral serine/threonine kinase inhibitor, suppresses signaling through PKCβ/PI3K/AKT pathways, induces apoptosis, reduces proliferation, and suppresses tumor-induced angiogenesis. Patients and methods: Patients with relapsed/refractory MCL, and no more than four regimens of prior therapy, received 500 mg enzastaurin, orally, once daily. Results: Sixty patients, median age 66 years (range 45–85), Eastern Cooperative Oncology Group performance status of zero to two (48% had baseline International Prognostic Index of 3–5), were enrolled. Most patients had prior CHOP-like chemotherapy and/or rituximab (median = 2 regimens). No drug-related deaths occurred. There was one case each of grade 3 anemia, diarrhea, dyspnea, vomiting, hypotension, and syncope. Fatigue was the most common toxicity. Although no objective tumor responses occurred, 22 patients (37%, 95% CI 25% to 49%) were free from progression (FFP) for ≥3 cycles (one cycle = 28 days); 6 of 22 were FFP for >6 months. Two patients remain on treatment and FFP at >23 months. Conclusion: Freedom from progression for >6 months in six patients and a favorable toxicity profile with minimal hematological toxicity indicate that enzastaurin warrants evaluation as maintenance therapy and combination chemotherapy in MCL.</div>
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<term>B cell neoplasm</term>
<term>B-Lymphocyte</term>
<term>Enzastaurin</term>
<term>Human</term>
<term>Inhibitor</term>
<term>Mantle cell lymphoma</term>
<term>Phase II trial</term>
<term>Protein kinase C</term>
<term>Protein kinase Cβ</term>
<term>Relapse</term>
<term>Treatment</term>
<term>Treatment resistance</term>
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<term>Homme</term>
<term>Essai clinique phase II</term>
<term>Traitement</term>
<term>Enzastaurine</term>
<term>Protein kinase C</term>
<term>Inhibiteur</term>
<term>Récidive</term>
<term>Résistance traitement</term>
<term>Lymphome centrocytique</term>
<term>Lymphocyte B</term>
<term>Protein kinase Cβ</term>
<term>Hémopathie lymphoïde B</term>
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<div type="abstract" xml:lang="en">Background: Protein kinase C beta (PKCβ), a pivotal enzyme in B-cell signaling and survival, is overexpressed in most cases of mantle cell lymphoma (MCL). Activation of P13K/AKT pathway is involved in pathogenesis of MCL. Enzastaurin, an oral serine/threonine kinase inhibitor, suppresses signaling through PKCβ/P13K/AKT pathways, induces apoptosis, reduces proliferation, and suppresses tumor-induced angiogenesis. Patients and methods: Patients with relapsed/refractory MCL, and no more than four regimens of prior therapy, received 500 mg enzastaurin, orally, once daily. Results: Sixty patients, median age 66 years (range 45-85), Eastern Cooperative Oncology Group performance status of zero to two (48% had baseline International Prognostic Index of 3-5), were enrolled. Most patients had prior CHOP-like chemotherapy and/or rituximab (median = 2 regimens). No drug-related deaths occurred. There was one case each of grade 3 anemia, diarrhea, dyspnea, vomiting, hypotension, and syncope. Fatigue was the most common toxicity. Although no objective tumor responses occurred, 22 patients (37%, 95% Cl 25% to 49%) were free from progression (FFP) for ≥3 cycles (one cycle = 28 days); 6 of 22 were FFP for >6 months. Two patients remain on treatment and FFP at >23 months. Conclusion: Freedom from progression for >6 months in six patients and a favorable toxicity profile with minimal hematological toxicity indicate that enzastaurin warrants evaluation as maintenance therapy and combination chemotherapy in MCL.</div>
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<affiliation>
<wicri:noCountry code="syntax">???</wicri:noCountry>
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<affiliation wicri:level="1">
<country wicri:rule="url">France</country>
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<author>
<name sortKey="Seymour, J F" sort="Seymour, J F" uniqKey="Seymour J" first="J. F." last="Seymour">J. F. Seymour</name>
<affiliation wicri:level="4">
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<wicri:regionArea>Hematology, Peter Maccallum Cancer Center, East Melbourne, and University of Melbourne</wicri:regionArea>
<placeName>
<settlement type="city">Melbourne</settlement>
<region type="état">Victoria (État)</region>
</placeName>
<orgName type="university">Université de Melbourne</orgName>
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</author>
<author>
<name sortKey="Kluin Nelemans, H C" sort="Kluin Nelemans, H C" uniqKey="Kluin Nelemans H" first="H. C." last="Kluin-Nelemans">H. C. Kluin-Nelemans</name>
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<wicri:regionArea>Hematology, University Medical Center Groningen, University of Groningen</wicri:regionArea>
<placeName>
<settlement type="city">Groningue (ville)</settlement>
<region>Groningue (province)</region>
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<orgName type="university">Université de Groningue</orgName>
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<name sortKey="Grigg, A" sort="Grigg, A" uniqKey="Grigg A" first="A." last="Grigg">A. Grigg</name>
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<wicri:regionArea>Clinical Hematology and Medical Oncology, Royal Melbourne Hospital, Melbourne, Victoria</wicri:regionArea>
<wicri:noRegion>Victoria</wicri:noRegion>
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<name sortKey="Wolf, M" sort="Wolf, M" uniqKey="Wolf M" first="M." last="Wolf">M. Wolf</name>
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<wicri:noCountry code="subField">Kassel</wicri:noCountry>
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<name sortKey="Pfreundschuh, M" sort="Pfreundschuh, M" uniqKey="Pfreundschuh M" first="M." last="Pfreundschuh">M. Pfreundschuh</name>
<affiliation wicri:level="1">
<country xml:lang="fr">Allemagne</country>
<wicri:regionArea>Onkologie, Hematology, Klin Immunologie & Rheumatologie, Universitatskliniken Des Saarlandes, Homburg/Saar</wicri:regionArea>
<wicri:noRegion>Homburg/Saar</wicri:noRegion>
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</author>
<author>
<name sortKey="Tilly, H" sort="Tilly, H" uniqKey="Tilly H" first="H." last="Tilly">H. Tilly</name>
<affiliation wicri:level="1">
<country xml:lang="fr">France</country>
<wicri:regionArea>Centre Henri Becquerel, Rouen Cedex</wicri:regionArea>
<wicri:noRegion>Rouen Cedex</wicri:noRegion>
<wicri:noRegion>Rouen Cedex</wicri:noRegion>
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</author>
<author>
<name sortKey="Raemaekers, J" sort="Raemaekers, J" uniqKey="Raemaekers J" first="J." last="Raemaekers">J. Raemaekers</name>
<affiliation wicri:level="3">
<country>Pays-Bas</country>
<placeName>
<settlement type="city">Nimègue</settlement>
<region type="province" nuts="2">Gueldre</region>
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<wicri:orgArea>Hematology, University Medical Centre Nijmegen</wicri:orgArea>
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<author>
<name sortKey="Van T Veer, M B" sort="Van T Veer, M B" uniqKey="Van T Veer M" first="M. B." last="Van T Veer">M. B. Van T Veer</name>
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<wicri:regionArea>Hematology, Erasmus Medisch Centrum, Rotterdam</wicri:regionArea>
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<settlement type="city">Rotterdam</settlement>
<region nuts="2" type="province">Hollande-Méridionale</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Milpied, N" sort="Milpied, N" uniqKey="Milpied N" first="N." last="Milpied">N. Milpied</name>
<affiliation>
<wicri:noCountry code="subField">Cedex</wicri:noCountry>
</affiliation>
</author>
<author>
<name sortKey="Cartron, G" sort="Cartron, G" uniqKey="Cartron G" first="G." last="Cartron">G. Cartron</name>
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<country xml:lang="fr">France</country>
<wicri:regionArea>Hematology, and Cell Therapy, Chru De Tours Hopital Bretonneau, Tours Cedex</wicri:regionArea>
<wicri:noRegion>Tours Cedex</wicri:noRegion>
<wicri:noRegion>Tours Cedex</wicri:noRegion>
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</author>
<author>
<name sortKey="Pezzutto, A" sort="Pezzutto, A" uniqKey="Pezzutto A" first="A." last="Pezzutto">A. Pezzutto</name>
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<country xml:lang="fr">Allemagne</country>
<wicri:regionArea>Med Klinic M.S.Hematologie/Oncologie, Universitatsklinikum Charite Med, Berlin</wicri:regionArea>
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<region type="land" nuts="3">Berlin</region>
<settlement type="city">Berlin</settlement>
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<name sortKey="Spencer, A" sort="Spencer, A" uniqKey="Spencer A" first="A." last="Spencer">A. Spencer</name>
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<country xml:lang="fr">Australie</country>
<wicri:regionArea>Hematology and BMT, The Alfred Hospital, Melbourne</wicri:regionArea>
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<settlement type="city">Melbourne</settlement>
<region type="état">Victoria (État)</region>
</placeName>
</affiliation>
</author>
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<name sortKey="Reyes, F" sort="Reyes, F" uniqKey="Reyes F" first="F." last="Reyes">F. Reyes</name>
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<wicri:noRegion>Creteil Cedex</wicri:noRegion>
<wicri:noRegion>Creteil Cedex</wicri:noRegion>
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</author>
<author>
<name sortKey="Dreyling, M" sort="Dreyling, M" uniqKey="Dreyling M" first="M." last="Dreyling">M. Dreyling</name>
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<country xml:lang="fr">Allemagne</country>
<wicri:regionArea>Klinikum Grosshadern der Ludwig-Maximilians-Universitat, Munchen</wicri:regionArea>
<wicri:noRegion>Munchen</wicri:noRegion>
<wicri:noRegion>Munchen</wicri:noRegion>
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<monogr></monogr>
<series>
<title level="j">Annals of Oncology</title>
<idno type="ISSN">0923-7534</idno>
<idno type="eISSN">1569-8041</idno>
<imprint>
<publisher>Oxford University Press</publisher>
<date type="published" when="2007-09-28">2007-09-28</date>
<biblScope unit="volume">19</biblScope>
<biblScope unit="issue">2</biblScope>
<biblScope unit="page" from="247">247</biblScope>
<biblScope unit="page" to="253">253</biblScope>
</imprint>
<idno type="ISSN">0923-7534</idno>
</series>
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<idno type="ISSN">0923-7534</idno>
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<textClass></textClass>
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<front>
<div type="abstract">Background: Protein kinase C beta (PKCβ), a pivotal enzyme in B-cell signaling and survival, is overexpressed in most cases of mantle cell lymphoma (MCL). Activation of PI3K/AKT pathway is involved in pathogenesis of MCL. Enzastaurin, an oral serine/threonine kinase inhibitor, suppresses signaling through PKCβ/PI3K/AKT pathways, induces apoptosis, reduces proliferation, and suppresses tumor-induced angiogenesis. Patients and methods: Patients with relapsed/refractory MCL, and no more than four regimens of prior therapy, received 500 mg enzastaurin, orally, once daily. Results: Sixty patients, median age 66 years (range 45–85), Eastern Cooperative Oncology Group performance status of zero to two (48% had baseline International Prognostic Index of 3–5), were enrolled. Most patients had prior CHOP-like chemotherapy and/or rituximab (median = 2 regimens). No drug-related deaths occurred. There was one case each of grade 3 anemia, diarrhea, dyspnea, vomiting, hypotension, and syncope. Fatigue was the most common toxicity. Although no objective tumor responses occurred, 22 patients (37%, 95% CI 25% to 49%) were free from progression (FFP) for ≥3 cycles (one cycle = 28 days); 6 of 22 were FFP for >6 months. Two patients remain on treatment and FFP at >23 months. Conclusion: Freedom from progression for >6 months in six patients and a favorable toxicity profile with minimal hematological toxicity indicate that enzastaurin warrants evaluation as maintenance therapy and combination chemotherapy in MCL.</div>
</front>
</TEI>
</ISTEX>
</double>
</record>

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