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Epitranscriptomics & Cancer Adaptation : A.David

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Our research work focuses on the contribution of post-transcriptional mechanisms on cancer cell adaptation, in particular RNA epigenetic & translational control.

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Group name EquipeCG
Item Type Journal Article
Title Safety and Efficacy of Nivolumab in Brain Metastases From Renal Cell Carcinoma: Results of the GETUG-AFU 26 NIVOREN Multicenter Phase II Study
Creator Flippot et al.
Author Ronan Flippot
Author Cécile Dalban
Author Brigitte Laguerre
Author Delphine Borchiellini
Author Sylvie Négrier
Author Christine Chevreau
Author Florence Joly
Author Lionnel Geoffrois
Author Sylvain Ladoire
Author Hakim Mahammedi
Author Marine Gross-Goupil
Author Elise Deluche
Author Frank Priou
Author Mathieu Laramas
Author Philippe Barthélémy
Author Bérengère Narciso
Author Stéphane Oudard
Author Marina Chenot
Author Florence Tantot
Author Sylvie Chabaud
Author Bernard Escudier
Author Laurence Albiges
Abstract PURPOSE: Nivolumab is standard of care for patients with metastatic clear cell renal cell carcinoma (ccRCC) after failure of antiangiogenic therapies, but its activity on brain metastases from ccRCC remains unknown, because these patients were excluded from pivotal studies. We aimed to assess the activity of nivolumab in this population. METHODS: The GETUG-AFU 26 NIVOREN phase II trial assessed the activity and safety of nivolumab in patients with metastatic ccRCC who failed vascular endothelial growth factor-directed therapies (ClinicalTrials.gov identifier: NCT03013335). Patients with asymptomatic brain metastases were prospectively identified and underwent dedicated brain evaluation. Two cohorts were constituted: cohort A comprised patients with previously untreated brain metastases, and cohort B comprised patients whose brain metastases underwent prior therapy. The primary end point was intracranial response rate in cohort A. RESULTS: Seventy-three patients with brain metastases were included: 39 in cohort A and 34 in cohort B. Intracranial response rate was 12% in cohort A; no objective response was reported in patients with brain lesions that were multiple or larger than 1 cm. Median intracranial progression-free survival was 2.7 months (95% CI, 2.3 to 4.6 months) in cohort A and 4.8 months (95% CI, 3.0 to 8.0 months) in cohort B, with adjusted hazard ratio of 2.04 (95% CI, 1.08 to 3.83). Overall survival rate at 12 months was 67% (95% CI, 49.6% to 79.1%) in cohort A and 59% (95% CI, 40.6% to 73.2%) in cohort B. Most patients in cohort A (72%) needed subsequent focal brain therapy. Nivolumab was well tolerated, with no unexpected toxicity. CONCLUSION: Nivolumab activity is limited in patients with untreated brain metastases from ccRCC. Brain imaging and focal therapy should be considered before immune checkpoint inhibitors in patients with metastatic ccRCC.
Publication Journal of Clinical Oncology: Official Journal of the American Society of Clinical Oncology
Volume 37
Issue 23
Pages 2008-2016
Date Aug 10, 2019
Journal Abbr J. Clin. Oncol.
Language eng
DOI 10.1200/JCO.18.02218
ISSN 1527-7755
Short Title Safety and Efficacy of Nivolumab in Brain Metastases From Renal Cell Carcinoma
Library Catalog PubMed
Extra 00000 PMID: 31194611
Tags Bristo-Myers Squibb, clinic
Date Added 2019/10/10 - 10:46:57
Date Modified 2019/10/24 - 16:06:36
Notes and Attachments PubMed entry (Attachment)


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