Congrès Targeted Anticancer Therapies — TAT 2015

Z. Ajgal, A. Bellesoeur, C. Baylot, C. Bigenwald, A. Brunot, E. Carton, E. De Guillebon, A. De Nonneville, J. Martin-Babau, R. Flippot, P. Gougis, L. Mahjoubi, N. Marques, L. Larrouquère, E. Pons, L. Verlingue, M. Viala, C. Vicier, A. Vinceneux, A. VozyP. Lavaud, C. Ferté

Résultats de recherche: Contribution à un journalArticleRevue par des pairs

Résumé

The TAT (Targeted Anticancer Therapies) Congress Conference was held in Paris, March 2–4 2015. Once again immunotherapy had the place of honor with PD-1/PD-L1 inhibitors, CSF-1 receptor inhibitor, adoptive immunotherapy, and development of combinations. The challenge is to identify the patients who could best respond to the immunotherapies. Among other drugs of interest, we can name cyclin-dependant kinase inhibitors or DNA methylation targeting drugs as well as PARP inhibitors or ATR inhibitors. Finally, a third generation of tyrosine-kinase inhibitors (TKI) is being assessed to overcome acquired resistance to the first TKI; such as rociletinib for lung cancer with T790M mutation. Molecular screening has proved its benefit in clinic routine with the MOSCATO-01 trial results; and new radiological and radiomic criteria are being validated to evaluate the tumoral response for patients who are treated by immunotherapy or targeted therapies.

Titre traduit de la contributionTargeted Anticancer Therapies — TAT 2015 Congress minutes
langue originaleFrançais
Pages (de - à)299-307
Nombre de pages9
journalOncologie
Volume17
Numéro de publication7-8
Les DOIs
étatPublié - 28 juil. 2015
Modification externeOui

mots-clés

  • Imaging
  • Immunotherapy
  • Personalized Medicine
  • Resistance
  • Targeted therapies

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