Characterization and spatial distribution of infiltrating lymphocytes in medullary, and lymphocyte-predominant triple negative breast cancers

Autor: A. Alfaro, C. Catelain, H. El-Masri, P. Rameau, M. Lacroix-Triki, JY. Scoazec, V. Marty, F. Mosele, B. Pistilli

Publikováno v: npj Breast Cancer, Vol 10, Iss 1, Pp 1-8 (2024)

Abstract Medullary carcinoma of the breast (MedBC) is a rare histological type that accounts for less than 5% of all invasive breast cancers. Here, we performed an exploratory study aimed to determine whether imaging mass cytometry (IMC) can be used

Externí odkaz: https://doaj.org/article/e16cc33190c840d1876403ee3c5e73a3

Clinical utility of circulating tumor DNA sequencing with a large panel: a National Center for Precision Medicine (PRISM) study

Autor: A. Bayle, L. Belcaid, M. Aldea, D. Vasseur, F. Peyraud, C. Nicotra, A. Geraud, M. Sakkal, L. Seknazi, L. Cerbone, F. Blanc-Durand, J. Hadoux, F. Mosele, M. Tagliamento, A. Bernard-Tessier, B. Verret, C. Smolenschi, R. Clodion, N. Auger, P.M. Romano, A. Gazzah, M.N. Camus, J. Micol, O. Caron, A. Hollebecque, Y. Loriot, B. Besse, L. Lacroix, E. Rouleau, S. Ponce, J.C. Soria, F. Barlesi, F. Andre, A. Italiano

Publikováno v: Annals of Oncology. 34:389-396

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::468af5b997d59fe42966e3f0dcb283f6
https://doi.org/10.1016/j.annonc.2023.01.008

The Influence of Cancer Molecular Subtypes and Treatment on the Mutation Spectrum in Metastatic Breast Cancers

Autor: F. Mosele, Bojana Stefanovska, Alicia Tran-Dien, Tony Sourisseau, Fabrice Andre, Benjamin Verret

Publikováno v: Cancer Research. 80:3062-3069

Next-generation sequencing has sparked the exploration of cancer genomes, with the aim of discovering the genetic etiology of the disease and proposing rationally designed therapeutic interventions. Driver gene alterations have been comprehensively c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae35eb111a823f2ec0a61a1ef406d098
https://doi.org/10.1158/0008-5472.can-19-3260

Detection of additional occult malignancy through profiling of ctDNA in late-stage cancer patients

Autor: Arnaud Bayle, C. Parisi, Antoine Italiano, Antoine Hollebecque, Loic Verlingue, Etienne Rouleau, Clémentine Sarkozy, S. Ponce, Pernelle Lavaud, Christophe Massard, F. Blanc-Durand, Mihaela Aldea, L. Cerbone, Y. Loriot, F. Mosele, M. Sakkal, Jean-Charles Soria, Ludovic Lacroix, D. Vasseur

Publikováno v: Annals of oncology : official journal of the European Society for Medical Oncology. 32(12)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae70d565620e7107446704c873dea64e
https://pubmed.ncbi.nlm.nih.gov/34509616

Recommendations for the use of next-generation sequencing (NGS) for patients with metastatic cancers: a report from the ESMO Precision Medicine Working Group

Autor: Aldo Scarpa, Albrecht Stenzinger, Nikhil Wagle, F. Mosele, S. Jezdic, A. Bayle, Fabrice Barlesi, Etienne Rouleau, Funda Meric-Bernstam, J.-Y. Douillard, Joaquin Mateo, Ivan Bièche, Julia Bonastre, Fabrice Andre, Jordi Remon, Stefan Michiels, Jorge S. Reis-Filho, Martijn P. Lolkema, Mark E. Robson, Nicola Normanno, C. B. Westphalen, R. Dienstmann

Publikováno v: Annals of Oncology
Annals of Oncology, Elsevier, 2020, 31, pp.1491-1505. ⟨10.1016/j.annonc.2020.07.014⟩
Annals of Oncology, 31(11), 1491-1505. Elsevier Ltd.

Next-generation sequencing (NGS) allows sequencing of a high number of nucleotides in a short time frame at an affordable cost. While this technology has been widely implemented, there are no recommendations from scientific societies about its use in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4cc8b09fd353f4a0ad4725894240a808
https://hal.archives-ouvertes.fr/hal-03493959