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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 EquipeCTCS
Item Type Journal Article
Title Real-world clinical and survival outcomes of patients with early relapsed triple-negative breast cancer from the ESME national cohort
Creator Grinda et al.
Author Thomas Grinda
Author Alison Antoine
Author William Jacot
Author Paul-Henri Cottu
Author Jean-Sébastien Frenel
Author Audrey Mailliez
Author Florence Dalenc
Author Anthony Goncalves
Author Florian Clatot
Author Marie-Ange Mouret Reynier
Author Christelle Levy
Author Jean-Marc Ferrero
Author Isabelle Desmoulins
Author Lionel Uwer
Author Thierry Petit
Author Christelle Jouannaud
Author Monica Arnedos
Author Michaël Chevrot
Author Coralie Courtinard
Author Olivier Tredan
Author Etienne Brain
Author David Pérol
Author Barbara Pistilli
Author Suzette Delaloge
Abstract BACKGROUND: Early metastatic relapse of triple-negative breast cancer (mTNBC) after anthracyclins and/or taxanes based (A/T) primary treatment represents a highly aggressive cancer situation requiring urgent characterisation and handling. Epidemio-Strategy-Medico-Economical-Metastatic Breast Cancer (ESME-MBC) database, a multicenter, national, observational cohort (NCT03275311) provides recent data on this entity. METHODS: All ESME patients diagnosed between 2008 and 2020 with mTNBC occurring as a relapse after a systemic neoadjuvant/adjuvant taxane and/or anthracycline-based chemotherapy were included. Early relapses were defined by a metastatic diagnosis up to 12 months of the end of neo/adjuvant A/T chemotherapy. We assessed overall survival (OS) and progression-free-survival under first-line treatment (PFS1) by early versus late relapse (?12 months). RESULTS: Patients with early relapse (N = 881, 46%) were younger and had a larger tumour burden at primary diagnosis than those with late relapses (N = 1045). Early relapse rates appeared stable over time. Median OS was 10.1 months (95% CI 9.3-10.9) in patients with early relapse versus 17.1 months (95% CI 15.7-18.2) in those with late relapse (adjusted hazard-ratio (aHR): 1.92 (95% CI 1.73-2.13); p < 0.001). The median PFS1 was respectively 3.1 months (95% CI 2.9-3.4) and 5.3 months (95% CI 5.1-5.8); (aHR: 1.66; [95% CI 1.50-1.83]; p < 0.001). Among early relapsed patients, a higher number of metastatic sites, visceral disease but not treatment types, were independently associated with a poorer OS. CONCLUSION: These real-world data provide strong evidence on the dismal prognosis, higher treatment resistance and major unmet medical need associated with early relapsed mTNBC. Database registration: clinicaltrials.gov Identifier NCT032753.
Publication European Journal of Cancer (Oxford, England: 1990)
Volume 189
Pages 112935
Date 2023-08
Journal Abbr Eur J Cancer
Language eng
DOI 10.1016/j.ejca.2023.05.023
ISSN 1879-0852
Library Catalog PubMed
Extra PMID: 37385070
Tags Antibiotics, Antineoplastic, Antineoplastic Combined Chemotherapy Protocols, Breast Neoplasms, Chronic Disease, clinic, ESME cohort, Female, Humans, Neoplasm Recurrence, Local, Prognosis, Progression-Free Survival, Real-world data, Triple Negative Breast Neoplasms, Triple-negative breast cancer
Date Added 2023/10/16 - 15:10:44
Date Modified 2023/10/16 - 17:27:15
Notes and Attachments PubMed entry (Attachment)


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