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- Publications
- Influence
Predictive correlates of response to the anti-PD-L1 antibody MPDL3280A in cancer patients
- R. Herbst, Jean-Charles Soria, +19 authors F. S. Hodi
- Biology, Medicine
- Nature
- 27 November 2014
The development of human cancer is a multistep process characterized by the accumulation of genetic and epigenetic alterations that drive or reflect tumour progression. These changes distinguish… Expand
Dendritic cell-derived exosomes as maintenance immunotherapy after first line chemotherapy in NSCLC
- B. Besse, M. Charrier, +25 authors N. Chaput
- Medicine
- Oncoimmunology
- 12 August 2015
ABSTRACT Dendritic cell-derived exosomes (Dex) are small extracellular vesicles secreted by viable dendritic cells. In the two phase-I trials that we conducted using the first generation of Dex… Expand
Dendritic cell-derived exosomes for cancer therapy.
- J. Pitt, F. André, +4 authors L. Zitvogel
- Medicine
- The Journal of clinical investigation
- 1 April 2016
DC-derived exosomes (Dex) are nanometer-sized membrane vesicles that are secreted by the sentinel antigen-presenting cells of the immune system: DCs. Like DCs, the molecular composition of Dex… Expand
PARP inhibition enhances tumor cell–intrinsic immunity in ERCC1-deficient non–small cell lung cancer
- R. Chabanon, G. Muirhead, +20 authors S. Postel-Vinay
- Chemistry, Medicine
- The Journal of clinical investigation
- 1 March 2019
The cyclic GMP-AMP synthase/stimulator of IFN genes (cGAS/STING) pathway detects cytosolic DNA to activate innate immune responses. Poly(ADP-ribose) polymerase inhibitors (PARPi) selectively target… Expand
Phase 1 study of JNJ-42756493, a pan-fibroblast growth factor receptor (FGFR) inhibitor, in patients with advanced solid tumors.
- Rastislav Bahleda, R. Dienstmann, +12 authors J. Tabernero
- Medicine
- 20 May 2014
2501 Background: JNJ-42756493 is an orally bioavailable FGFR 1, 2, 3 and 4 inhibitor with nanomolar antitumor activity in cell lines and in vivo models with FGFR pathway aberration. Methods: This… Expand
Genomic and transcriptomic profiling expands precision cancer medicine: the WINTHER trial
- J. Rodon, Jean-Charles Soria, +22 authors R. Kurzrock
- Medicine
- Nature Medicine
- 22 April 2019
Precision medicine focuses on DNA abnormalities, but not all tumors have tractable genomic alterations. The WINTHER trial (NCT01856296) navigated patients to therapy on the basis of fresh… Expand
IGF-1R Targeting Increases the Antitumor Effects of DNA-Damaging Agents in SCLC Model: An Opportunity to Increase the Efficacy of Standard Therapy
- C. Ferté, Y. Loriot, +11 authors E. Deutsch
- Biology, Medicine
- Molecular Cancer Therapeutics
- 2 May 2013
Insulin-like growth factor receptor-1 (IGF-1R) inhibition could be a relevant therapeutic approach in small cell lung cancer (SCLC) given the importance of an IGF-1R autocrine loop and its role in… Expand
Quantitative proteomics profiling of primary lung adenocarcinoma tumors reveals functional perturbations in tumor metabolism.
- M. Pernemalm, L. de Petris, +11 authors J. Lehtiö
- Biology, Medicine
- Journal of proteome research
- 13 August 2013
In this study, we have analyzed human primary lung adenocarcinoma tumors using global mass spectrometry to elucidate the biological mechanisms behind relapse post surgery. In total, we identified… Expand
Dependence on Phosphoinositide 3-Kinase and RAS-RAF Pathways Drive the Activity of RAF265, a Novel RAF/VEGFR2 Inhibitor, and RAD001 (Everolimus) in Combination
- P. Mordant, Y. Loriot, +5 authors E. Deutsch
- Biology, Medicine
- Molecular Cancer Therapeutics
- 1 February 2010
Activation of phosphatidylinositol-3-kinase (PI3K)-AKT and Kirsten rat sarcoma viral oncogene homologue (KRAS) can induce cellular immortalization, proliferation, and resistance to anticancer… Expand
Transcriptional Analysis of an E2F Gene Signature as a Biomarker of Activity of the Cyclin-Dependent Kinase Inhibitor PHA-793887 in Tumor and Skin Biopsies from a Phase I Clinical Study
- Giada. A. Locatelli, R. Bosotti, +13 authors A. Isacchi
- Biology, Medicine
- Molecular Cancer Therapeutics
- 27 April 2010
A transcriptional signature of the pan–cyclin-dependent kinase (Cdk) inhibitor PHA-793887 was evaluated as a potential pharmacodynamic and/or response biomarker in tumor and skin biopsies from… Expand