Paule Augereau

ORCID: 0000-0002-4748-0799
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About
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Research Areas
  • Advanced Breast Cancer Therapies
  • Cancer Treatment and Pharmacology
  • HER2/EGFR in Cancer Research
  • Genetic factors in colorectal cancer
  • Glioma Diagnosis and Treatment
  • Ovarian cancer diagnosis and treatment
  • Brain Metastases and Treatment
  • Cancer Genomics and Diagnostics
  • PI3K/AKT/mTOR signaling in cancer
  • Breast Cancer Treatment Studies
  • Pancreatic and Hepatic Oncology Research
  • Cancer Immunotherapy and Biomarkers
  • PARP inhibition in cancer therapy
  • Colorectal and Anal Carcinomas
  • Lung Cancer Research Studies
  • Cancer-related Molecular Pathways
  • Chronic Lymphocytic Leukemia Research
  • Peptidase Inhibition and Analysis
  • Testicular diseases and treatments
  • Endometrial and Cervical Cancer Treatments
  • Monoclonal and Polyclonal Antibodies Research
  • BRCA gene mutations in cancer
  • Colorectal Cancer Treatments and Studies
  • Reproductive Biology and Fertility
  • Multiple and Secondary Primary Cancers

Institut de Cancérologie de l'Ouest
2016-2025

Roche (Switzerland)
2021

Centre Hospitalier Universitaire de Rennes
2019

Centre Jean Perrin
2013-2019

Centre Eugène Marquis
2018-2019

Centre Hospitalier Universitaire de Nantes
2018-2019

Centre Hospitalier Départemental Vendée
2019

Roche (France)
2018-2019

Centre Hospitalier Universitaire de Limoges
2019

Centre Hospitalier Universitaire de Clermont-Ferrand
2019

Abstract Background Metastatic breast cancer (MBC) behaviour differs depending on hormone receptors (HR) and human epidermal growth factor receptor (HER2) statuses. Methods The kinetics of central nervous system (CNS) metastases (CNS metastasis-free survival, CNSM-FS) subsequent patient’s prognosis (overall OS) according to the molecular subtype were retrospectively assessed in 16703 MBC patients ESME nationwide multicentre database (Kaplan–Meier method). Results CNS occurred 4118 (24.6%)...

10.1038/s41416-019-0619-y article EN cc-by British Journal of Cancer 2019-11-13

We proposed in 2005 that androgens replace oestrogens as the driver steroids a subgroup of triple-negative breast cancer (TNBC) with androgen receptor (AR) expression called molecular apocrine (MA) or luminal (LAR). Here, we report analysis clinical trial evaluating antitumour activity anti-androgen darolutamide MA cancer. Our aim was to assess benefit patients AR-positive TNBCs defined by immunohistochemistry and RNA profiling. In this multicentre, non-comparative, randomised, phase 2...

10.1016/s1470-2045(24)00737-x article EN cc-by-nc-nd The Lancet Oncology 2025-02-01

Abstract Missense mutations in the polymerase epsilon (POLE) gene have been reported to generate proofreading defects resulting an ultramutated genome and sensitize tumors checkpoint blockade immunotherapy. However, many POLE-mutated do not respond such treatment. To better understand link between POLE mutation variants response immunotherapy, we prospectively assessed efficacy of nivolumab a multicenter clinical trial patients bearing advanced mismatch repair–proficient solid tumors. We...

10.1158/2159-8290.cd-21-0521 article EN Cancer Discovery 2022-04-05

<h3>Importance</h3> Endometrial cancer is often hormone-dependent and treated with aromatase inhibitors. The PI3K-AKT-mTOR pathway deregulation observed in endometrial drives hormonal resistance, thus supporting the rationale of combining mTOR inhibitor endocrine therapy. <h3>Objective</h3> To evaluate safety efficacy vistusertib combination anastrozole treatment women hormone receptor−positive recurrent or metastatic cancer. <h3>Design, Settings, Participants</h3> VICTORIA study was a...

10.1001/jamaoncol.2022.1047 article EN JAMA Oncology 2022-05-12

Purpose: Investigates the link between HER2 status and histological response after neoadjuvant chemotherapy in patients with early TNBC. Methods: We retrieved clinical anatomopathological data retrospectively from 449 treated for first time standard unilateral BC 2005 2020. The primary endpoint was pathological complete (pCR, i.e., ypT0 ypN0), according to status. Secondary endpoints included invasive disease-free survival (I-DFS) overall (OS). Results: 437 were included, 121 (27.7%) had...

10.3390/cancers14102509 article EN Cancers 2022-05-19

Leptomeningeal metastasis (LM) is a rare complication of metastatic breast cancer (MBC), with high morbidity/mortality rates. Our study aimed to describe the largest-to-date real-life population MBC patients treated intrathecal (IT) therapy and evaluate prognostic models.The Epidemiological Strategy Medical Economics (ESME) database (NCT03275311) includes all consecutive who have initiated treatment for since 2008. Overall survival (OS) IT was estimated using Kaplan-Meier method. Prognostic...

10.1016/j.esmoop.2021.100150 article EN cc-by-nc-nd ESMO Open 2021-05-11

Everolimus is the first oral targeted therapy widely used in advanced HR+/HER2− breast cancer. We sought to evaluate impact of everolimus-based on overall survival ESME-MBC database, a national metastatic cancer cohort that collects retrospective data using clinical trial-like methodology including quality assessments. compared 1693 patients having received everolimus 5928 not exposed same period. Overall was evaluated according treatment line, and propensity score with inverse probability...

10.3390/cancers15041191 article EN Cancers 2023-02-13
Judith Balmañà Peter A. Fasching Fergus J. Couch Suzette Delaloge Sana Intidhar Labidi‐Galy and 95 more Joyce O’Shaughnessy Yeon Hee Park Andrea Eisen Benoît You Hughes Bourgeois Anthony Gonçalvès Zoe Kemp Angela Swampillai Tomasz Jankowski Joohyuk Sohn Elena Poddubskaya Guzel Mukhametshina Sercan Aksoy Constanta Timcheva Tjoung‐Won Park‐Simon Antonio Antón-Torres Ellie John Katherine Baria Isabel Gibson Karen A. Gelmon Tatyana Koynova Vasil Popov Constanta Timcheva Antoaneta Tomova Andrea Eisen Karen A. Gelmon Julie Lemieux Paule Augereau Fernando Bazán Celia Roemer Becuwe Hugues Bourgeois Camille Chakiba Mohamad Chehimi Caroline Cheneau Florence Dalenc Éléonore De Guillebon Thibault De La Motte Rouge Jean‐Sébastien Frénel Anthony Gonçalvès Julien Grenier Anne Claire Hardy-Bessard R. Lamy Christelle Lévy Alain Lortholary Audrey Mailliez Jacques Médioni Anne Patsouris Dominique Spaëth Luís Teixeira Isabelle Tennevet Laurence Venat‐Bouvet Cristian Villanueva Benoît You Johannes Ettl Peter A. Fasching Bernd Gerber Claus Hanusch Oliver Hoffmann Tjoung‐Won Park‐Simon Wolfram Malter Mattea Reinisch Joke Tio Pauline Wimberger Katalin Boér Magdolna Dank Alberto Ballestrero Giampaolo Bianchini Laura Biganzoli Roberto Bordonaro Francesco Cognetti Enrico Cortesi Michelino De Laurentiis Sabino De Placido Luca Gianni Valentina Guarneri Paulo Henrique Marchetti Filippo Montemurro Anna Maria Mosconi Giuseppe Naso Fabio Puglisi Armando Santoro Claudio Zamagni Hiroji Iwata Seung-Jin Kim Seigo Nakamura Yee Soo Chae Eun Kyung Cho Jee Hyun Kim Seock‐Ah Im Keun Seok Lee Yeon Hee Park Joohyuk Sohn Tomasz Byrski Tomasz Huzarski Tomasz Jankowski

The interim analysis of the phase IIIb LUCY trial demonstrated clinical effectiveness olaparib in patients with germline BRCA-mutated (gBRCAm), human epidermal growth factor receptor 2 (HER2)-negative metastatic breast cancer (mBC), median progression-free survival (PFS) 8.11 months, which was similar to that arm III OlympiAD (7.03 months). This prespecified provides final overall (OS) and safety data.

10.1007/s10549-023-07165-x article EN cc-by Breast Cancer Research and Treatment 2023-12-19

Pazopanib (PZB), an anti-angiogenic tyrosine kinase inhibitor, has shown activity in pre-treated advanced glioblastomas (GBM). Biological and clinical data support the evaluation of PZB earlier stage disease. The objective PAZOGLIO trial (NCT02331498) is to evaluate safety (phase I) efficacy II) combined with Temozolomide (TMZ) during maintenance phase as defined by "Stupp protocol" GBM patients after complete or partial resection surgery. Here, we report updated results I. a prospective...

10.1016/j.esmoop.2024.102291 article EN cc-by-nc-nd ESMO Open 2024-02-01

Abstract Purpose Previous studies have reported the benefit of dual HER2-targeting combined to neoadjuvant chemotherapy in HER2-amplified breast cancer (HER2 + BC). Moreover, besides cardiac toxicity following their association Trastuzumab, anthracyclines may not profit all patients. The NeoTOP study was designed evaluate complementary action Trastuzumab and Pertuzumab, relevance an anthracycline-based regimen according TOP2A amplification status. Methods Open-label, multicentre, phase II...

10.1007/s10549-024-07285-y article EN cc-by Breast Cancer Research and Treatment 2024-03-07
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