45 results on '"Guy, Jean-Baptiste"'
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2. Les médecines alternatives complémentaires en oncologie
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Bosacki, Claire, Vallard, Alexis, Gras, Mathilde, Daguenet, Elisabeth, Morisson, Stéphanie, Méry, Benoite, Jmour, Omar, Guy, Jean-Baptiste, and Magné, Nicolas
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- 2019
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3. Analogues de la LH-RH dans le traitement hormonal adjuvant dans les cancers du sein localisés de la femme pré-ménopausée : la fin d’une controverse pour de nouvelles recommandations ?
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Daguenet, Elisabeth, Jmour, Omar, Vallard, Alexis, Guy, Jean-Baptiste, Jacquin, Jean-Philippe, Méry, Benoîte, and Magné, Nicolas
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- 2019
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4. Innovations en radiothérapie : un regard sur 2018
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Vial, Nicolas, Vallard, Alexis, Jmour, Omar, Rehailia-Blanchard, Amel, Ben Mrad, Majed, Trone, Jane-Chloe, Daguenet, Elisabeth, Guy, Jean-Baptiste, and Magné, Nicolas
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- 2019
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5. Cancer du rein et radiothérapie : radiorésistance et au-delà
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Mery, Benoîte, Rancoule, Chloé, Rowinski, Elise, Bosacki, Claire, Vallard, Alexis, Guy, Jean-Baptiste, and Magné, Nicolas
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- 2018
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6. Radiothérapie et immunothérapie
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Rancoule, Chloé, Vallard, Alexis, Jmour, Omar, Vial, Nicolas, Guillaume, Elodie, Guy, Jean-Baptiste, and Magné, Nicolas
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- 2018
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7. Radiothérapie et biomarqueurs de la réparation de l’ADN
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Vallard, Alexis, Rancoule, Chloé, Guy, Jean-Baptiste, Espenel, Sophie, Sauvaigo, Sylvie, Rodriguez-Lafrasse, Claire, and Magné, Nicolas
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- 2017
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8. Altération de la réparation de l’ADN et cancer
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Rancoule, Chloé, Vallard, Alexis, Guy, Jean-Baptiste, Espenel, Sophie, Sauvaigo, Sylvie, Rodriguez-Lafrasse, Claire, and Magné, Nicolas
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- 2017
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9. Immunothérapie : après le focus sur les voies de signalisation, l’activation d’un système
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Bernichon, Emilie, Rancoule, Chloé, Vallard, Alexis, Langrand-Escure, Julien, Mery, Benoîte, Guy, Jean-Baptiste, and Magné, Nicolas
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- 2017
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10. Les 50 ans du cisplatine
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Rancoule, Chloé, Guy, Jean-Baptiste, Vallard, Alexis, Ben Mrad, Majed, Rehailia, Amel, and Magné, Nicolas
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- 2017
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11. Principe de prises en charge du carcinome à cellules de Merkel et place de la radiothérapie
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Rehailia-Blanchard, Amel, Pigné, Grégoire, Guy, Jean-Baptiste, Vallard, Alexis, El Meddeb Hamrouni, Anis, Rancoule, Chloé, and Magné, Nicolas
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- 2017
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12. Prédiction de la gravité des neutropénies fébriles par le score de MASCC : une étude de cohorte rétrospective
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Cervetti, Louise, Vallard, Alexis, Le Moulec, Sylvestre, Espenel, Sophie, Falk, Alexander Tuan, Ben Mrad, Majed, Guy, Jean-Baptiste, Diao, Peng, Méry, Benoîte, Langrand-Escure, Julien, Ferrand, François-Régis, Rivoirard, Romain, Ceccaldi, Bernard, Védrine, Lionel, Magné, Nicolas, and Chargari, Cyrus
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- 2016
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13. Cellules souches tumorales : aspects radiothérapeutiques et ciblage thérapeutique
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Méry, Benoîte, Rancoule, Chloé, Guy, Jean-Baptiste, Espenel, Sophie, Wozny, Anne-Sophie, Simonet, Stéphanie, Vallard, Alexis, Alphonse, Gersende, Ardail, Dominique, Rodriguez-Lafrasse, Claire, and Magné, Nicolas
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- 2016
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14. Radiosensibilité et/ou résistance des cancers ORL : aspects biologiques
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Guy, Jean-Baptiste, Rancoule, Chloé, Méry, Benoîte, Espenel, Sophie, Wozny, Anne-Sophie, Simonet, Stéphanie, Vallard, Alexis, Alphonse, Gersende, Ardail, Dominique, Rodriguez-Lafrasse, Claire, and Magné, Nicolas
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- 2016
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15. Personnes âgées et radiothérapie : une synthèse de la littérature
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Vallard, Alexis, Guy, Jean-Baptiste, Espenel, Sophie, Langrand-Escure, Julien, Trone, Jane-Chloé, Méry, Benoîte, Moriceau, Guillaume, Rivoirard, Romain, de Laroche, Guy, Chargari, Cyrus, and Magné, Nicolas
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- 2015
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16. Cancers rares et nouvelles techniques de radiothérapie
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Espenel, Sophie, Trone, Jane-Chloé, Vallard, Alexis, Guy, Jean-Baptiste, Moriceau, Guillaume, Méry, Benoîte, Langrand-Escure, Julien, Rivoirard, Romain, de Laroche, Guy, Chargari, Cyrus, and Magné, Nicolas
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- 2015
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17. La radiothérapie induit-elle une agressivité accrue des cellules tumorales du glioblastome?
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Falk, Alexander T., Moncharmont, Coralie, Guilbert, Matthieu, Guy, Jean-Baptiste, Alphonse, Gersende, Trone, Jane-Chloé, Rivoirard, Romain, Gilormini, Marion, Toillon, Robert-Alain, Rodriguez-Lafrasse, Claire, and Magné, Nicolas
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- 2014
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18. Évaluation du dépistage des cancers de la femme et du dépistage après 75 ans dans le département de la Loire
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Swalduz, Aurélie, Guibert, Cyril, Trone, Jane-Chloé, Guichard, Jean-Baptiste, Rivoirard, Romain, Pacaut, Cécile, Méry, Benoîte, Guy, Jean-Baptiste, Eddekkaoui, Houda, Fournel, Pierre, de Laroche, Guy, Merrouche, Yacine, and Magné, Nicolas
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- 2014
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19. Carcinosarcomes gynécologiques : revue générale et principes de prise en charge
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Guy, Jean-Baptiste, Trone, Jane-Chloé, Casteillo, François, Forest, Fabien, Pacaut, Cécile, Moncharmont, Coralie, Espenel, Sophie, Vallard, Alexis, Langrand Escure, Julien, Collard, Olivier, Peoc’h, Michel, and Magné, Nicolas
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- 2014
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20. Réentraînement à l’activité physique dans la prise en charge globale du cancer du sein : étude pilote monocentrique
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Sorg, Marine, Trone, Jane-Chloé, Méry, Benoîte, Guichard, Jean-Baptiste, Rivoirard, Romain, Pacaut, Cécile, Guy, Jean-Baptiste, Eddekkaoui, Houda, Collard, Olivier, Bosacki, Claire, Jacquin, Jean-Philippe, Guy, Jean-Michel, and Magné, Nicolas
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- 2014
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21. Les mélanomes digestifs primitifs : y a-t-il un consensus ?
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Eddekkaoui, Houda, Guy, Jean-Baptiste, Falk, Alexander T., Lahmar, Rima, Trone, Jane-Chloé, Bahadoor Mohun, R.K, Kullab, Sharif, Collard, Olivier, Rivoirard, Romain, Moriceau, Guillaume, Vignot, Stéphane, and Magné, Nicolas
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- 2014
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22. Mélanomes du tractus génital féminin : état des lieux
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Trone, Jane-Chloé, Guy, Jean-Baptiste, Mery, Benoite, Langrand Escure, Julien, Lahmar, Rima, Moncharmont, Coralie, Rivoirard, Romain, Semay, Tiphaine, Chauleur, Céline, Collard, Olivier, Vignot, Stéphane, and Magné, Nicolas
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- 2014
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23. Prise en charge du cancer primitif du vagin chez la femme de plus de 70 ans : intérêt d’une association radiothérapie-curiethérapie
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Moncharmont, Coralie, Levy, Antonin, Guy, Jean-Baptiste, Auberdiac, Pierre, Robles, Aurélie, Malkoun, Nadia, Chargari, Cyrus, Pacaut, Cécile, Jacquin, Jean-Philippe, Chauleur, Céline, de Laroche, Guy, and Magné, Nicolas
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- 2013
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24. Facteurs de radiorésistance des cellules souches cancéreuses et perspectives de radiosensibilisation : l’exemple du glioblastome
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Chargari, Cyrus, Moncharmont, Coralie, Lévy, Antonin, Guy, Jean-Baptiste, Bertrand, Gérald, Guilbert, Matthieu, Rousseau, Claire, Védrine, Lionel, Alphonse, Gersende, Toillon, Robert-Alain, Rodriguez-Lafrasse, Claire, Deutsch, Éric, and Magné, Nicolas
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- 2012
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25. Évaluation des pratiques professionnelles : améliorer la prise en charge de la douleur liée au cancer en oncologie radiothérapie
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Auberdiac, Pierre, Levy, Antonin, Guy, Jean-Baptiste, Malkoun, Nadia, Moncharmont, Coralie, Chargari, Cyrus, Michaud, Patrick, De Laroche, Guy, and Magné, Nicolas
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- 2012
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26. La distribution spatiale des radicaux libres oxygénés permet d’expliquer la différence d’activation des processus d’invasion/migration des cellules souches cancéreuses en réponse aux photons et aux ions carbone
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Wozny, Anne-Sophie, Alphonse, Gersende, Vares, Guillaume, Monini, Caterina, Guy, Jean-Baptiste, Fujimori, Akira, Monboisse, Jean-Claude, Magné, Nicolas, Beuve, Michael, Nakajima, Tetsuo, Rodriguez-Lafrasse, Claire, Centre Hospitalier Lyon Sud [CHU - HCL] (CHLS), Hospices Civils de Lyon (HCL), Institut de Physique Nucléaire de Lyon (IPNL), Centre National de la Recherche Scientifique (CNRS)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3), PRISME (PRISME), Institut de Physique des 2 Infinis de Lyon (IP2I Lyon), Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Centre National de la Recherche Scientifique (CNRS)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Centre National de la Recherche Scientifique (CNRS), National Institute of Radiobiological Sciences, Institut de Cancérologie Lucien Neuwirth, CHU Saint-Etienne, Matrice extracellulaire et dynamique cellulaire - UMR 7369 (MEDyC), SFR CAP Santé (Champagne-Ardenne Picardie Santé), Université de Reims Champagne-Ardenne (URCA)-Université de Picardie Jules Verne (UPJV)-Université de Reims Champagne-Ardenne (URCA)-Université de Picardie Jules Verne (UPJV)-Université de Reims Champagne-Ardenne (URCA)-Centre National de la Recherche Scientifique (CNRS), and Rayet, Béatrice
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Hypoxie ,[PHYS.PHYS.PHYS-MED-PH] Physics [physics]/Physics [physics]/Medical Physics [physics.med-ph] ,irradiation photonique ,ions carbone ,[SDV.CAN] Life Sciences [q-bio]/Cancer ,[CHIM.RADIO] Chemical Sciences/Radiochemistry ,[PHYS.PHYS.PHYS-MED-PH]Physics [physics]/Physics [physics]/Medical Physics [physics.med-ph] ,ROS ,[SDV.CAN]Life Sciences [q-bio]/Cancer ,transition épithélio-mésenchymateuse ,cellules souches cancéreuses ,[CHIM.RADIO]Chemical Sciences/Radiochemistry - Abstract
International audience; Objectifs : La transition épithélio-mésenchymateuse (EMT) est le mécanisme qui permet l’échappement des cellules cancéreuses de la tumeur pour former des métastases. Alors que la radiothérapie conventionnelle favorise l’invasion/migration des cellules souches cancéreuses (CSCs), les ions carbone diminuent ces processus. Cependant, les CSCs, radio/chimiorésistantes sont localisées dans des niches hypoxiques tumorales où l’hypoxie amplifie les effets biologiques liés à la radioresistance. Ainsi, la compréhension des mécanismes différentiels impliqués dans la réponse aux photons et aux ions carbone, particulièrement en hypoxie, permettrait de mieux comprendre le processus d’échappement tumoral.Méthodes : Les processus de motilité, d’invasion/migration et les voies de signalisation de l’EMT ont été étudiés en réponse à une irradiation par photons et ions carbone pour deux lignées de tumeurs des voies aéro-digestives supérieures et leur sous-population de CSCs, en normoxie et hypoxie.Resultats : Après avoir confirmé en normoxie l’augmentation de l’invasion/migration en réponse aux photons et la diminution après irradiation par ions carbone, nous avons montré que sous hypoxie, les deux types d’irradiation conduisent à une diminution du processus. Afin de comprendre cette réponse différentielle, les profils de phosphorylation des voies Akt/mTor, STAT3 et ERK/p38/MSK impliquées dans l’EMT ont été établis. En réponse aux photons, l’activation des cascades de kinases est importante pour les 3 voies alors qu’elle l’est plus faiblement en hypoxie, et pas du tout en réponse aux ions carbone quelle que soit la tension en oxygène.Conclusion : Nos résultats montrent un profil d’activation des trois principales voies de l’EMT fonction du type d’irradiation et de la tension en oxygène. La production de ROS, uniformément répartie dans la cellule en réponse aux photons permet l’activation des voies contrairement aux ions carbone où les ROS sont uniquement localisés dans la trace.
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- 2018
27. Ciblage des cellules souches cancéreuses dans le cancer ORL: effet synergique du cetuximab à l’ABT-199 en association à l’irradiation photonique
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Guy, Jean-Baptiste, Espenel, Sophie, Wozny, Anne-Sophie, Battiston-Montagne, Priscillia, Ardail, Dominique, Alphonse, Gersende, Rodriguez-Lafrasse, Claire, Magné, Nicolas, Institut de Cancérologie Lucien Neuwirth, CHU Saint-Etienne, Institut de Physique Nucléaire de Lyon (IPNL), Centre National de la Recherche Scientifique (CNRS)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3), PRISME (PRISME), Institut de Physique des 2 Infinis de Lyon (IP2I Lyon), Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Centre National de la Recherche Scientifique (CNRS)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Centre National de la Recherche Scientifique (CNRS), Centre Hospitalier Lyon Sud [CHU - HCL] (CHLS), Hospices Civils de Lyon (HCL), and Rayet, Béatrice
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[PHYS.PHYS.PHYS-MED-PH] Physics [physics]/Physics [physics]/Medical Physics [physics.med-ph] ,[SDV.CAN] Life Sciences [q-bio]/Cancer ,[PHYS.PHYS.PHYS-MED-PH]Physics [physics]/Physics [physics]/Medical Physics [physics.med-ph] ,[SDV.CAN]Life Sciences [q-bio]/Cancer - Abstract
National audience; Les cellules souches cancéreuses (CSCs) de cancer ORL, sous-population hautement migratoire, semblent être à l’origine de la résistance aux traitements. L’objectif du travail était d’étudier l’effet synergique d’un inhibiteur spécifique de Bcl-2, l’ABT-199, avec un anticorps monoclonal anti-EGFR, le cetuximab, en association avec l’irradiation photonique sur une lignée de cancer ORL et sa sous-population de CSCs.
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- 2017
28. Evaluation préclinique en modèle 3D de l’association de l’ABT-199 au cetuximab et aux radiations ionisantes sur les cellules cancéreuses ORL
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Espenel, Sophie, Guy, Jean-Baptiste, Wozny, Anne-Sophie, Battiston-Montagne, Priscillia, Rancoule, Chloé, Alphonse, Gersende, Ardail, Dominique, Rodriguez-Lafrasse, Claire, Magné, Nicolas, Institut de Cancérologie Lucien Neuwirth, CHU Saint-Etienne, Institut de Physique Nucléaire de Lyon (IPNL), Centre National de la Recherche Scientifique (CNRS)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3), PRISME (PRISME), Institut de Physique des 2 Infinis de Lyon (IP2I Lyon), Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Centre National de la Recherche Scientifique (CNRS)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Centre National de la Recherche Scientifique (CNRS), Centre Hospitalier Lyon Sud [CHU - HCL] (CHLS), Hospices Civils de Lyon (HCL), and Rayet, Béatrice
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[PHYS.PHYS.PHYS-MED-PH] Physics [physics]/Physics [physics]/Medical Physics [physics.med-ph] ,[SDV.CAN] Life Sciences [q-bio]/Cancer ,[PHYS.PHYS.PHYS-MED-PH]Physics [physics]/Physics [physics]/Medical Physics [physics.med-ph] ,[SDV.CAN]Life Sciences [q-bio]/Cancer - Abstract
International audience; Objectif de l’étude: Les cellules souches cancéreuses (CSCs) de cancer ORL, sous-population hautement migratoire, semblent être à l’origine de la résistance aux traitements. Nous avons montré dans un précédent travail, sur des modèles de culture cellulaire en 2D, que l’association de l’ABT-199 au cetuximab et à l’irradiation photonique semblait inhiber de façon synergique la prolifération, l’invasion et la migration de la lignée radiorésistante SQ20B et de leur sous-population de CSCs. L’objectif de notre travail était de confirmer ces résultats dans un modèle de culture cellulaire en 3D, plus transposable aux modèles in vivo.
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- 2017
29. Ciblage des cellules souches cancéreuses dans les cancers ORL : effet synergique de l’ABT-199 et du cetuximab en association à la radiothérapie photonique
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Guy, Jean-Baptiste, Espenel, Sophie, Wozny, Anne-Sophie, Battiston-Montagne, Priscillia, Rancoule, Chloé, Alphonse, Gersende, Ardail, Dominique, Rodriguez-Lafrasse, Claire, Magné, Nicolas, Rayet, Béatrice, Institut de Cancérologie Lucien Neuwirth, CHU Saint-Etienne, Institut de Physique Nucléaire de Lyon (IPNL), Centre National de la Recherche Scientifique (CNRS)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3), Centre Hospitalier Lyon Sud [CHU - HCL] (CHLS), and Hospices Civils de Lyon (HCL)
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Bcl2 ,[PHYS.PHYS.PHYS-MED-PH] Physics [physics]/Physics [physics]/Medical Physics [physics.med-ph] ,[SDV.CAN] Life Sciences [q-bio]/Cancer ,sphéroïdes ,[PHYS.PHYS.PHYS-MED-PH]Physics [physics]/Physics [physics]/Medical Physics [physics.med-ph] ,invasion/migration ,cancer ORL ,[SDV.CAN]Life Sciences [q-bio]/Cancer ,radiothérapie ,cellules souches cancéreuses - Abstract
National audience; Objet : Les cellules souches cancéreuses (CSCs) de cancer ORL, sous-population hautement migratoire, semblent être à l’origine de la résistance aux traitements. L’objectif de ce travail était d’étudier l’effet synergique d’un inhibiteur spécifique de Bcl-2, l’ABT-199, avec un anticorps monoclonal anti-EGFR, le cetuximab, en association à une irradiation photonique sur une lignée de cancer ORL et sa sous-population de CSCs.Méthodes : La sous-population de CSCs de la lignée SQ20B a été isolée par double tri. Les cellules ont été exposées à de l’ABT-199 10μM et/ou du cetuximab 5nM +/- irradiation photonique à 4 Gy. La prolifération des SQ20B et SQ20B/CSCs a été mesurée par vidéomicroscopie. Les analyses de la migration et de l’invasion ont été réalisées par test de blessure avec et sans matrigel (IncuCyte). L’apoptose a été évaluée par le test des caspases 3/7 en microscopie à fluorescence. Les données ont été validées grâce à un modèle 3D de culture en sphéroïdes. L’activation des voies de signalisation intracellulaires (Phospho-AKT et Phospho-MEK1/2), et des voies anti-apoptotiques (Bcl-2 et Bcl-xl) a été étudiée en réponse aux traitements par western-blot (WES).Résultat : Le cetuximab inhibe la prolifération, l’invasion et la migration des SQ20B mais n’a aucun effet sur la sous-population de SQ20B/CSCs. A l’inverse, l’ABT-199 inhibe significativement ces processus dans les SQ20B/CSCs. L’ABT-199 a peu d’effet sur les SQ20B, en revanche il potentialise l’effet du cetuximab dans les deux populations. De plus, l’irradiation photonique à 4 Gy majore l’effet de l’ABT-199 et renforce l’effet de l’association thérapeutique. Ces résultats s’expliquent par la surexpression de l’EGFR dans les SQ20B et de Bcl-2 et Bcl-xl dans les SQ20B/CSCs.Conclusion : L’association ABT-199+Cetuximab combinée à l’irradiation photonique inhibe de façon synergique la prolifération, la migration et l’invasion des SQ20B et de leur sous-population de CSCs, et semble prometteuse en clinique.
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- 2017
30. Ciblage de la famille HER dans les cancers ORL : inhibition de la prolifération cellulaire et de l’invasion-migration cellulaire en réponse à l’association cetuximab-pertuzumab combinée à l’irradiation photonique
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Guy, Jean-Baptiste, Méry, Benoîte, Wozny, Anne-Sophie, Battiston-Montagne, Priscillia, Ardail, Dominique, Alphonse, Gersende, Rodriguez-Lafrasse, Claire, Magné, Nicolas, Institut de Cancérologie Lucien Neuwirth, CHU Saint-Etienne, Institut de Physique Nucléaire de Lyon (IPNL), Centre National de la Recherche Scientifique (CNRS)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3), Centre Hospitalier Lyon Sud [CHU - HCL] (CHLS), Hospices Civils de Lyon (HCL), and Rayet, Béatrice
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[SDV.CAN] Life Sciences [q-bio]/Cancer ,Famille HER ,[SDV.CAN]Life Sciences [q-bio]/Cancer ,Cellules souches cancéreuses ,Invasion/Migration ,Cancer ORL - Abstract
National audience; Objet : Les cancers épidermoïdes ORL sont associés à un fort taux de récidive loco-régionale et métastatique. Les cellules souches cancéreuses (CSCs), sous-population hautement migratoire, semblent être une hypothèse majeure à l’origine de la résistance aux traitements. L’objectif du travail était de comparer l’efficacité du blocage pan-HER par une association cetuximab-pertuzumab associé à l’irradiation photonique dans les processus d’invasion et migration de la lignée SQ20B et sa sous-population souche.Méthodes : La sous-population de CSCs de la lignée SQ20B a été isolée par double tri. La prolifération des cellules SQ20B et SQ20B/CSCs a été étudiée après traitement au cetuximab 5nM et/ou pertuzumab 20microg/mL +/- irradiation photonique à 10 Gy. L’analyse de la migration et de l’invasion a été réalisée par test de blessure avec et sans matrigel (IncuCyte(R)). L’activation de l’EGFR (Tyr1068) et des voies de signalisation intracellulaires (Phospho-AKT et Phospho-MEK1/2) a été étudiée en réponse aux traitements par western-blot (WES(R)).Résultat : Le cetuximab inhibe la prolifération cellulaire des cellules SQ20B et non celle de la sous-population souche. L’association cetuximab-pertuzumab inhibe significativement la prolifération des cellules SQ20B et SQ20B/CSCs. La double association cetuximab-pertuzumab associée à l’irradiation 10Gy inhibe significativement la migration et l’invasion des deux populations cellulaires. Le double traitement inhibe la phosphorylation d’EGFR dans les deux populations. Les cellules SQ20B expriment fortement phospho-AKT à l’inverse des SQ20B/CSCs qui expriment phospho-MEK1/2. Enfin, l’association cetuximab-pertuzumab-10Gy inhibe fortement l’expression de phospho-AKT et phospho-MEK1/2.Conclusion : Le double traitement cetuximab-pertuzumab combiné à l’irradiation photonique inhibe significativement la prolifération, la migration et l’invasion de la lignée SQ20B et sa sous-population souche.This work was supported by LabEx PRIMES, France Hadron
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- 2016
31. Cellules souches cancéreuses : responsables des processus d’invasion et migration des cancers des voies aéro-digestives supérieures mais condamnées par l’association d’une irradiation par ions carbone au cetuximab
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Moncharmont, Coralie, Guy, Jean-Baptiste, Wozny, Anne-Sophie, Battiston-Montagne, Priscillia, Beuve, Michael, Alphonse, Gersende, Magné, Nicolas, Rodriguez-Lafrasse, Claire, Institut de Cancérologie Lucien Neuwirth, CHU Saint-Etienne, Ciblage thérapeutique en Oncologie (EA3738), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon, Centre Hospitalier Lyon Sud [CHU - HCL] (CHLS), Hospices Civils de Lyon (HCL), Institut de Physique Nucléaire de Lyon (IPNL), Centre National de la Recherche Scientifique (CNRS)-Université Claude Bernard Lyon 1 (UCBL), and Université de Lyon-Université de Lyon-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)
- Subjects
[PHYS.PHYS.PHYS-MED-PH]Physics [physics]/Physics [physics]/Medical Physics [physics.med-ph] ,[SDV.CAN]Life Sciences [q-bio]/Cancer - Abstract
International audience; Les cancers épidermoïdes de la tête et du cou (HNSCC) sont associés à un fort taux de récidives loco-régionales et métastatiques. Les cellules souches cancéreuses (CSCs), sous-population dotée d’un potentiel migratoire important, semblent être une hypothèse majeure à l’origine de la résistance aux traitements. L’objectif du travail était de comparer l’efficacité de l’hadronthérapie par ions carbone à la radiothérapie conventionnelle, associées ou non au cetuximab (inhibiteur du récepteur de l’epidermal growth factor ou EGFR) sur une population de CSCs de lignée HNSCC, sur leur prolifération, et leur potentiel invasif et migratoire.
- Published
- 2015
32. [Stereotactic body radiotherapy: Passing fad or revolution?]
- Author
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Vallard A, Vial N, Jmour O, Rehailia-Blanchard A, Trone JC, Sotton S, Daguenet E, Guy JB, and Magné N
- Subjects
- Adrenal Gland Neoplasms radiotherapy, Adrenal Gland Neoplasms secondary, Brain Neoplasms radiotherapy, Brain Neoplasms secondary, Carcinoma, Hepatocellular radiotherapy, Carcinoma, Non-Small-Cell Lung radiotherapy, Combined Modality Therapy methods, Forecasting, Humans, Immunotherapy methods, Kidney Neoplasms radiotherapy, Liver Neoplasms radiotherapy, Liver Neoplasms secondary, Lung Neoplasms radiotherapy, Lung Neoplasms secondary, Pancreatic Neoplasms, Radiotherapy Dosage, Spinal Cord Neoplasms radiotherapy, Neoplasms radiotherapy, Radiosurgery methods, Radiosurgery trends
- Abstract
Stereotactic body radiotherapy (SBRT) is a young technology that can deliver a high dose of radiation to the target, utilizing either a single dose or a small number of fractions with a high degree of precision within the body. Various technical solutions co-exist nowadays, with particular features, possibilities and limitations. Health care authorities have currently validated SBRT in a very limited number of locations, but many indications are still under investigation. It is therefore challenging to accurately appreciate the SBRT therapeutic index, its place and its role within the anticancer therapeutic arsenal. The aim of the present review is to provide SBRT definitions, current indications, and summarize the future ways of research. There are three validated indications for SBRT: un-resecable T1-T2 non small cell lung cancer, <3 slow-growing pulmonary metastases secondary to a stabilized primary, and the tumours located close to the medulla. In other situations, the benefit of SBRT is still to be demonstrated. One of the most promising way of research is the ablative treatment of oligo metastatic cancers, with recent studies suggesting a survival benefit. Furthermore, the most recent data suggest that SBRT is safe. Finally, the SBRT combined with immune therapies is promising, since it could theoretically trigger the adaptative anticancer response., (Copyright © 2019 Société Française du Cancer. Published by Elsevier Masson SAS. All rights reserved.)
- Published
- 2020
- Full Text
- View/download PDF
33. [Complementary and alternative medicines in cancer patients].
- Author
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Bosacki C, Vallard A, Gras M, Daguenet E, Morisson S, Méry B, Jmour O, Guy JB, and Magné N
- Subjects
- Acupuncture Therapy, Homeopathy, Humans, Complementary Therapies, Neoplasms therapy
- Abstract
Complementary and alternative medicines (CAMs) play more and more a significant role both in France and all over the world. Yet, their definition and their role in cancer treatments legitimately raise concerns. This article aims at establishing a picture of the CAMs admitted by the French Medical Board as well as those which are new or in common medical practices in France. We start with a brief reminder of their origin, their status and how they are used. Then, we review the literature about some of the best clinical trials using CAMs in cancer patients. To finish, we try to understand what makes CAMs so thrilling, but also why they create controversy and which common points they may have with conventional medicine., (Copyright © 2019 Société Française du Cancer. Published by Elsevier Masson SAS. All rights reserved.)
- Published
- 2019
- Full Text
- View/download PDF
34. [LHRH analogs in adjuvant endocrine therapy for pre-menopausal localized breast cancers: Ending the controversy for novel guidelines?]
- Author
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Daguenet E, Jmour O, Vallard A, Guy JB, Jacquin JP, Méry B, and Magné N
- Subjects
- Breast Neoplasms pathology, Chemotherapy, Adjuvant, Female, Gonadotropin-Releasing Hormone agonists, Humans, Ovary drug effects, Risk Assessment, Tamoxifen therapeutic use, Antineoplastic Agents, Hormonal therapeutic use, Aromatase Inhibitors therapeutic use, Breast Neoplasms drug therapy, Gonadotropin-Releasing Hormone analogs & derivatives, Practice Guidelines as Topic, Premenopause
- Abstract
Endocrine treatment represents the cornerstone of endocrine-sensitive pre-menopausal early breast cancer. The estrogen blockade plays a leading role in the therapeutic management with surgery, radiotherapy and selective antiestrogen treatment. For several years, selective estrogen receptor modulators, such as tamoxifen, have revolutionized medical care of hormone receptors-positive breast cancer and have conquered the therapeutic arsenal while becoming the gold standard of treatment. Other combinations associating the ovarian function suppression using LHRH agonists with tamoxifen or aromatase inhibitors have been recently investigated, leading to mitigated opinions regarding the clinical benefit of these associations. We propose here a comprehensive overview on existing data and their actualization concerning LHRH analogues, whilst emphasizing benefit-risk balance for this targeted population., (Copyright © 2019 Société Française du Cancer. Published by Elsevier Masson SAS. All rights reserved.)
- Published
- 2019
- Full Text
- View/download PDF
35. [Biomarkers of radiation-induced DNA repair processes].
- Author
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Vallard A, Rancoule C, Guy JB, Espenel S, Sauvaigo S, Rodriguez-Lafrasse C, and Magné N
- Subjects
- Ataxia Telangiectasia Mutated Proteins physiology, DNA Breaks, Double-Stranded, DNA Damage, DNA Repair Enzymes adverse effects, DNA Repair Enzymes physiology, DNA-Activated Protein Kinase physiology, Dose-Response Relationship, Radiation, Histones physiology, Humans, Nuclear Proteins physiology, Radiation Tolerance, Radiotherapy, Recombinational DNA Repair, Signal Transduction, Tumor Suppressor p53-Binding Protein 1 physiology, Biomarkers analysis, DNA radiation effects, DNA Repair
- Abstract
The identification of DNA repair biomarkers is of paramount importance. Indeed, it is the first step in the process of modulating radiosensitivity and radioresistance. Unlike tools of detection and measurement of DNA damage, DNA repair biomarkers highlight the variations of DNA damage responses, depending on the dose and the dose rate. The aim of the present review is to describe the main biomarkers of radiation-induced DNA repair. We will focus on double strand breaks (DSB), because of their major role in radiation-induced cell death. The most important DNA repair biomarkers are DNA damage signaling proteins, with ATM, DNA-PKcs, 53BP1 and γ-H2AX. They can be analyzed either using immunostaining, or using lived cell imaging. However, to date, these techniques are still time and money consuming. The development of "omics" technologies should lead the way to new (and usable in daily routine) DNA repair biomarkers., (Copyright © 2017 Société Française du Cancer. Published by Elsevier Masson SAS. All rights reserved.)
- Published
- 2017
- Full Text
- View/download PDF
36. [Impairment of DNA damage response and cancer].
- Author
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Rancoule C, Vallard A, Guy JB, Espenel S, Sauvaigo S, Rodriguez-Lafrasse C, and Magné N
- Subjects
- Antineoplastic Agents pharmacology, Cell Transformation, Neoplastic genetics, Clinical Trials, Phase III as Topic, Combined Modality Therapy, DNA, Neoplasm genetics, Humans, Mutation, Neoplasm Proteins antagonists & inhibitors, Neoplasm Proteins physiology, Neoplasms etiology, Neoplasms genetics, Neoplasms therapy, Poly(ADP-ribose) Polymerase Inhibitors pharmacology, Poly(ADP-ribose) Polymerase Inhibitors therapeutic use, Antineoplastic Agents therapeutic use, DNA Damage, DNA Repair drug effects, DNA, Neoplasm drug effects, Molecular Targeted Therapy, Neoplasms drug therapy
- Abstract
Maintaining the genetic integrity is a key process in cell viability and is enabled by a wide network of repair pathways. When this system is defective, it generates genomic instability and results in an accumulation of chromosomal aberrations and mutations that may be responsible for various clinical phenotypes, including susceptibility to develop cancer. Indeed, these defects can promote not only the initiation of cancer, but also allow the tumor cells to rapidly acquire mutations during their evolution. Several genes are involved in these damage repair systems and particular polymorphisms are predictive of the onset of cancer, the best described of them being BRCA. In addition to its impact on carcinogenesis, the DNA damage repair system is now considered as a therapeutic target of choice for cancer treatment, as monotherapy or in combination with other cytotoxic therapies, such as chemotherapies or radiotherapy. PARP inhibitors are nowadays the best known, but other agents are emerging in the field of clinical research. The enthusiasm in this area is coupled with promising results and a successful collaboration between clinicians and biologists would allow to optimize treatment plans in order to take full advantage of the DNA repair system modulation., (Copyright © 2017 Société Française du Cancer. Published by Elsevier Masson SAS. All rights reserved.)
- Published
- 2017
- Full Text
- View/download PDF
37. [50th anniversary of cisplatin].
- Author
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Rancoule C, Guy JB, Vallard A, Ben Mrad M, Rehailia A, and Magné N
- Subjects
- Antineoplastic Agents adverse effects, Antineoplastic Agents chemistry, Antineoplastic Agents pharmacology, Cisplatin adverse effects, Cisplatin chemistry, Cisplatin pharmacology, DNA Adducts, Drug Resistance, Neoplasm, History, 20th Century, History, 21st Century, Antineoplastic Agents history, Cisplatin history
- Abstract
We have just celebrated the 50th anniversary of cisplatin cytotoxic potential discovery. It is time to take stock… and it seems mainly positive. This drug, that revolutionized the treatment of many cancer types, continues to be the most widely prescribed chemotherapy. Despite significant toxicities, resistance mechanisms associated with treatment failures, and unresolved questions about its mechanism of action, the use of this cytotoxic agent remains unwavering. The interest concerning this "old" invincible drug has not yet abated. Indeed many research axes are in the news. New platinum salts agents are tested, new cisplatin formulations are developed to target tumor cells more efficiently, and new combinations are established to increase the cytotoxic potency of cisplatin or overcome the resistance mechanisms., (Copyright © 2016 Société Française du Cancer. Published by Elsevier Masson SAS. All rights reserved.)
- Published
- 2017
- Full Text
- View/download PDF
38. [Care of Merkel cell carcinoma and role of the radiotherapy].
- Author
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Rehailia-Blanchard A, Pigné G, Guy JB, Vallard A, El Meddeb Hamrouni A, Rancoule C, and Magné N
- Subjects
- Antineoplastic Agents therapeutic use, Carcinoma, Merkel Cell epidemiology, Carcinoma, Merkel Cell pathology, Carcinoma, Merkel Cell radiotherapy, Combined Modality Therapy, Humans, Practice Guidelines as Topic, Prognosis, Radiotherapy Dosage, Rare Diseases epidemiology, Rare Diseases pathology, Rare Diseases radiotherapy, Skin Neoplasms epidemiology, Skin Neoplasms pathology, Skin Neoplasms radiotherapy, Carcinoma, Merkel Cell therapy, Rare Diseases therapy, Skin Neoplasms therapy
- Abstract
Merkel cell carcinoma is a rare neuro-endocrine tumor of skin with a poor prognosis. Data available in literature are scarce. Current treatment for locoregional disease is based on combined treatment by surgery and radiotherapy. However these treatments are controversial. The aim of the present review is to sum up the different available studies and to compare national and international guidelines., (Copyright © 2016 Société Française du Cancer. Published by Elsevier Masson SAS. All rights reserved.)
- Published
- 2017
- Full Text
- View/download PDF
39. [Elderly patients and radiotherapy: A short review].
- Author
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Vallard A, Guy JB, Espenel S, Langrand-Escure J, Trone JC, Méry B, Moriceau G, Rivoirard R, de Laroche G, Chargari C, and Magné N
- Subjects
- Aged, Aged, 80 and over, France, Humans, Neoplasms classification, Patient Selection, Radiation Tolerance, Radiotherapy adverse effects, Health Transition, Neoplasms radiotherapy
- Abstract
The ageing of French population imposes to radiotherapists the challenge to treat older patients and to adjust their treatment. Unthinkable 30 years ago, radiation therapy concerns nowadays patients aged more than 90 years old. Oncogeriatric scales have been improved those last years without necessarily making sure that the right treatment is given to the right patient: if oncogeriatric scales use influences the final therapeutic decision, it does not define new target volumes, new doses, or new fractionation protocols. Except for some organs, there is not, for the moment, any consensus concerning geriatric population adapted treatments. This makes any therapeutic decision difficult. The present review has for objective to realise a report of the studies about favorable and unfavorable effects of radiation therapy amongst aged (>70 years old) or very aged (>90years old) population., (Copyright © 2015 Société Française du Cancer. Published by Elsevier Masson SAS. All rights reserved.)
- Published
- 2015
- Full Text
- View/download PDF
40. [Rare cancers and new radiotherapy techniques].
- Author
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Espenel S, Trone JC, Vallard A, Guy JB, Moriceau G, Méry B, Langrand-Escure J, Rivoirard R, de Laroche G, Chargari C, and Magné N
- Subjects
- Humans, Radiotherapy, Intensity-Modulated methods, Neoplasms radiotherapy, Radiosurgery methods, Radiotherapy, Conformal methods, Rare Diseases radiotherapy
- Abstract
Rare cancers represent about a quarter of all cancers diagnosed in Europe, and their incidence is increasing. Meanwhile, scientific advances provide techniques, which become more and more sophisticated in the domain of radiotherapy. Treatment options for radiotherapy rare cancers are increasing, but are not yet evaluated. The question of the appropriateness of treatment by modern radiotherapy techniques in rare cancers remains. There are a lot of cases reported in the literature for treating rare cancers by modern technology. These techniques are often used when anatomical and dosimetric constraints do not achieve optimal treatment by surgery or standard radiotherapy. In contrast, standard radiotherapy techniques also provide good results in terms of overall survival and tolerance. They are also less expensive and less complex in terms of dosimetry. The establishment of specialized centers in rare cancers seems essential to evaluate the appropriateness of the use of modern techniques in these cases. Currently, data from the literature does not provide an answer to this question., (Copyright © 2014 Société Française du Cancer. Published by Elsevier Masson SAS. All rights reserved.)
- Published
- 2015
- Full Text
- View/download PDF
41. [Assessment of screening in women cancers and in 75 years older in Loire department].
- Author
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Swalduz A, Guibert C, Trone JC, Guichard JB, Rivoirard R, Pacaut C, Méry B, Guy JB, Eddekkaoui H, Fournel P, de Laroche G, Merrouche Y, and Magné N
- Subjects
- Adult, Age Factors, Aged, Breast Neoplasms epidemiology, Colonic Neoplasms epidemiology, Female, France epidemiology, Health Care Surveys, Health Surveys, Humans, Lung Neoplasms epidemiology, Male, Middle Aged, Prostatic Neoplasms epidemiology, Uterine Cervical Neoplasms epidemiology, Vaginal Smears statistics & numerical data, Young Adult, Breast Neoplasms diagnosis, Colonic Neoplasms diagnosis, Lung Neoplasms diagnosis, Mass Screening statistics & numerical data, Prostatic Neoplasms diagnosis, Uterine Cervical Neoplasms diagnosis
- Abstract
In France, there is an important interregional disparity concerning participation to cancer screening programs. The aim of this study was to assess oncologic screening practices in Loire, a French rural department, in women and in the elderly (over age 74 years). For this, two surveys were conducted. The first one was regarding screening for breast, cervical and colorectal cancer in women over age 18 years living in Loire. The second survey was regarding onco-geriatric screening through two questionnaires : one for the elderly and the other for general practitioner (GP) of the department, evaluating screening for breast, colorectal, prostate, cervical and lung cancer. One hundred sixty six women were included in the first investigation mean age of 47.6 years. Ninety three point six per cent were screening for breast cancer, 19% received Human Papilloma virus vaccine, 83.1% were screening by Papanicolau smear for cervical cancer and finally, 51.7% were screening for colorectal cancer, among the one entering screening program criteria. In the second survey, 44 patients and 28 GP were included. Thirty-eight point six per cent of patients over 74 years continue screening. Only 11.4% were reluctant to screening and in 80% because of anxiety du to the results. Among GP, 50 % continued screening on two major criteria : life expectancy and performans status. The present study shows heterogeneity of screening in this department both rural and working class and gives us a societo-medical photography.
- Published
- 2014
- Full Text
- View/download PDF
42. [Radiation-induces increased tumor cell aggressiveness of tumors of the glioblastomas?].
- Author
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Falk AT, Moncharmont C, Guilbert M, Guy JB, Alphonse G, Trone JC, Rivoirard R, Gilormini M, Toillon RA, Rodriguez-Lafrasse C, and Magné N
- Subjects
- Brain Neoplasms pathology, Cell Line, Tumor radiation effects, Focal Adhesion Kinase 1 metabolism, Glioblastoma pathology, Heavy Ion Radiotherapy, Humans, Integrins metabolism, Photons therapeutic use, Receptors, Urokinase Plasminogen Activator metabolism, Signal Transduction radiation effects, Brain Neoplasms radiotherapy, Cell Movement radiation effects, Glioblastoma radiotherapy, Neoplasm Invasiveness pathology, Neoplasm Recurrence, Local, Photons adverse effects
- Abstract
Glioblastoma multiform is the most common and aggressive brain tumor with a worse prognostic. Ionizing radiation is a cornerstone in the treatment of glioblastome with chemo-radiation association being the actual standard. As a paradoxal effect, it has been suggested that radiotherapy could have a deleterious effect on local recurrence of cancer. In vivo studies have studied the effect of radiotherapy on biological modification and pathogenous effect of cancer cells. It seems that ionizing radiations with photon could activate oncogenic pathways in glioblastoma cell lines. We realized a review of the literature of photon-enhanced effect on invasion and migration of glioblastoma cells by radiotherapy.
- Published
- 2014
- Full Text
- View/download PDF
43. [Primary digestive melanomas: is there any consensus?].
- Author
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Eddekkaoui H, Guy JB, Falk AT, Lahmar R, Trone JC, Bahadoor MR, Kullab S, Collard O, Rivoirard R, Moriceau G, Vignot S, and Magné N
- Subjects
- Anus Neoplasms diagnosis, Anus Neoplasms pathology, Anus Neoplasms therapy, Bile Duct Neoplasms diagnosis, Bile Duct Neoplasms pathology, Consensus, Esophageal Neoplasms diagnosis, Esophageal Neoplasms pathology, Esophageal Neoplasms therapy, Humans, Intestinal Neoplasms diagnosis, Intestinal Neoplasms pathology, Intestinal Neoplasms therapy, Prognosis, Rectal Neoplasms diagnosis, Rectal Neoplasms pathology, Rectal Neoplasms therapy, Stomach Neoplasms diagnosis, Stomach Neoplasms pathology, Stomach Neoplasms therapy, Gastrointestinal Neoplasms diagnosis, Gastrointestinal Neoplasms pathology, Gastrointestinal Neoplasms therapy, Melanoma diagnosis, Melanoma pathology, Melanoma therapy, Rare Diseases diagnosis, Rare Diseases pathology, Rare Diseases therapy
- Abstract
In clinical practice and the literature, malignant melanoma usually appears in typical sites where melanocytes can be found: skin, eyes meninges and anal region. Malignant melanomas of the esophagus-gastrointestinal (EGI) tract are usually metastatic. Primary and diffuse EGI tract melanoma is rare and only a few descriptions of this presentation have been found in the literature. The prognosis of EGI tract melanoma is frightening because of late diagnosis and high malignancy potential. Treatment is based essentially on surgery. The objective of the present study is to specify the clinical and therapeutic aspects of primary digestive melanoma.
- Published
- 2014
- Full Text
- View/download PDF
44. [Management of vaginal carcinoma in patients over 70 years old: advantage of a radiotherapy-brachytherapy association].
- Author
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Moncharmont C, Levy A, Guy JB, Auberdiac P, Robles A, Malkoun N, Chargari C, Pacaut C, Jacquin JP, Chauleur C, de Laroche G, and Magné N
- Subjects
- Aged, Aged, 80 and over, Brachytherapy adverse effects, Carcinoma, Squamous Cell mortality, Carcinoma, Squamous Cell pathology, Cohort Studies, Female, Humans, Radiotherapy, Conformal adverse effects, Retrospective Studies, Treatment Outcome, Vaginal Neoplasms mortality, Vaginal Neoplasms pathology, Brachytherapy methods, Carcinoma, Squamous Cell radiotherapy, Radiotherapy, Conformal methods, Vaginal Neoplasms radiotherapy
- Abstract
Objective: Report and discuss the management of the primitive vaginal cancer in elderly adults at a single institute., Patients and Methods: Data from patients more than 70 year-old treated for a primitive vaginal cancer at the Institut de Cancérologie de la Loire Lucien-Neuwirth was retrospectively collected., Results: From August 1999 to January 2009, 9/24 patients treated for a primitive vaginal cancer had more than 70 year-old. The median age was 81 years (7-94 years). Most patients had a performance status less or equal to 1 (n=6), a squamous cell carcinoma (n=7) and a FIGO stage less or equal to II (n=6). All patients were treated with 3D external beam radiation, 3 received concurrent chemotherapy, 3 had a supplementary brachytherapy, and 6 had a colpohysterectomy. Among 7 evaluable patients, there were 4 complete responses, 2 partial responses and one progression. Main acute toxicities were gastrointestinal (n=5), urinary (n=3), general (n=3) and cutaneous (n=2). Three patients experienced late toxicities. Four patients had a local recurrence after a mean delay of 10.8 months. At last news, 4 patients were still alive and 4/5 deaths were related to the cancer. All (n=3) patients who received the combination of radiotherapy - brachytherapy were alive and disease-free. Median overall survival was 18 months., Discussion and Conclusions: Primitive vaginal cancers are rare and aggressive tumours. Our results suggested the feasibility of the combination of radiotherapy and brachytherapy for elderly patients. Prospective trials remain needed to better define and validate the optimal strategy, especially in elderly adults., (Copyright © 2013 Elsevier Masson SAS. All rights reserved.)
- Published
- 2013
- Full Text
- View/download PDF
45. [Cancer stem cells, cornerstone of radioresistance and perspectives for radiosensitization: glioblastoma as an example].
- Author
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Chargari C, Moncharmont C, Lévy A, Guy JB, Bertrand G, Guilbert M, Rousseau C, Védrine L, Alphonse G, Toillon RA, Rodriguez-Lafrasse C, Deutsch E, and Magné N
- Subjects
- AC133 Antigen, Antigens, CD metabolism, Cell Cycle, DNA Repair physiology, Glioblastoma metabolism, Glycoproteins metabolism, Humans, Neoplasm Proteins metabolism, Neoplastic Stem Cells cytology, Neoplastic Stem Cells metabolism, Peptides metabolism, Protein-Tyrosine Kinases metabolism, Radiation Tolerance physiology, Stem Cell Niche physiology, Tumor Microenvironment physiology, Glioblastoma radiotherapy, Neoplastic Stem Cells radiation effects, Radiation Tolerance drug effects, Radiation-Sensitizing Agents pharmacology, Signal Transduction physiology
- Abstract
Cancer stem cells are a subject of increasing interest in oncology. In particular, several data suggest that cancer stem cells are involved in the mechanisms of tumor radioresistance, and may explain the therapeutic failures after radiotherapy. Because of its poor prognosis and high recurrence rate after irradiation, glioblastoma model is often studied in the search for new radiosensitizers. There are several preclinical data suggesting that cancer stem cells could be a potential therapeutic target for improving the biological effectiveness of radiation therapy. Through the example of glioblastoma, we review the main signaling pathways involved in the mechanisms of radiation resistance of cancer stem cells and for which pharmacological targeting could potentially enhance tumor radiosensitivity.
- Published
- 2012
- Full Text
- View/download PDF
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