Targeted Anticancer Therapies - TAT 2015 Congress minutes

被引:0
|
作者
Ajgal, Z. [1 ]
Bellesoeur, A. [1 ]
Baylot, C. [1 ]
Bigenwald, C. [1 ]
Brunot, A. [1 ]
Carton, E. [1 ]
De Guillebon, E. [1 ]
De Nonneville, A. [1 ]
Martin-Babau, J. [1 ]
Flippot, R. [1 ]
Gougis, P. [1 ]
Mahjoubi, L. [1 ]
Marques, N. [1 ]
Larrouquere, L. [1 ]
Pons, E. [1 ]
Verlingue, L. [1 ]
Viala, M. [1 ]
Vicier, C. [1 ]
Vinceneux, A. [1 ]
Vozy, A. [1 ]
Lavaud, P. [1 ]
Ferte, C. [1 ,2 ]
机构
[1] AERIO, F-75014 Paris, France
[2] Gustave Roussy, F-94800 Villejuif, France
关键词
Targeted therapies; Immunotherapy; Resistance; Personalized Medicine; Imaging;
D O I
10.1007/s10269-015-2530-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:299 / 307
页数:9
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