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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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Added by celine.gongora
Group name EquipeCG
Item Type Journal Article
Title Development of immunotherapy in bladder cancer: present and future on targeting PD(L)1 and CTLA-4 pathways
Creator Rouanne et al.
Author Mathieu Rouanne
Author Nadine Houédé
Author Alexandra Masson-Lecomte
Author Pierre Colin
Author Géraldine Pignot
Author Stéphane Larré
Author Evanguelos Xylinas
Author Morgan Rouprêt
Author Yann Neuzillet
Abstract PURPOSE: Over the past 3 decades, no major treatment breakthrough has been reported for advanced bladder cancer. Recent Food and Drug Administration (FDA) approval of five immune checkpoint inhibitors in the management of advanced bladder cancer represent new therapeutic opportunities. This review examines the available data of the clinical trials leading to the approval of ICIs in the management of metastatic bladder cancer and the ongoing trials in advanced and localized settings. METHODS: A literature search was performed on PubMed and ClinicalTrials.gov combining the MeSH terms: 'urothelial carcinoma' OR 'bladder cancer', and 'immunotherapy' OR 'CTLA-4' OR 'PD-1' OR 'PD-L1' OR 'atezolizumab' OR 'nivolumab' OR 'ipilimumab' OR 'pembrolizumab' OR 'avelumab' OR 'durvalumab' OR 'tremelimumab'. Prospectives studies evaluating anti-PD(L)1 and anti-CTLA-4 monoclonal antibodies were included. RESULTS: Evidence-data related to early phase and phase III trials evaluating the 5 ICIs in the advanced urothelial carcinoma are detailed in this review. Anti-tumour activity of the 5 ICIs supporting the FDA approval in the second-line setting are reported. The activity of PD(L)1 inhibitors in the first-line setting in cisplatin-ineligible patients are also presented. Ongoing trials in earlier disease-states including non-muscle-invasive and muscle-invasive bladder cancer are discussed. CONCLUSIONS: Blocking the PD-1 negative immune receptor or its ligand, PD-L1, results in unprecedented rates of anti-tumour activity in patients with metastatic urothelial cancer. However, a large majority of patients do not respond to anti-PD(L)1 drugs monotherapy. Investigations exploring the potential value of predictive biomarkers, optimal combination and sequences are ongoing to improve such treatment strategies.
Publication World Journal of Urology
Volume 36
Issue 11
Pages 1727-1740
Date Nov 2018
Journal Abbr World J Urol
Language eng
DOI 10.1007/s00345-018-2332-5
ISSN 1433-8726
Short Title Development of immunotherapy in bladder cancer
Library Catalog PubMed
Extra PMID: 29855698
Tags AFU, Biomarkers, Bladder cancer, Carcinoma, Transitional Cell, clinic, CTLA-4, CTLA-4 Antigen, Disease-Free Survival, Female, Humans, Immune checkpoint inhibitors, Immunologic Factors, Immunotherapy, Male, Molecular Targeted Therapy, PD-1, PD-L1, Prognosis, Programmed Cell Death 1 Receptor, Risk Assessment, Survival Analysis, Treatment Outcome, Urinary Bladder Neoplasms, Urothelial cancer
Date Added 2019/10/10 - 10:48:39
Date Modified 2019/10/24 - 17:35:59
Notes and Attachments PubMed entry (Attachment)


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