Nathalie EBRAN

Dr. Nathalie EBRAN


Research Focus & Metrics

Academic Career Length

7Years (2020-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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23 November 2020 in Pharmaceuticals
Verified
Journal Article
Open access
PDF file
JGJocelyn Gal
Jocelyn Gal
GMGérard Milano
Gérard Milano
PBPatrick Brest
Patrick Brest
NENathalie EBRAN
Nathalie EBRAN
JGJulia Gilhodes
Julia Gilhodes
JPJean-Yves Pierga
Jean-Yves Pierga
The prospective multicenter COMET trial followed a cohort of 306 consecutive metastatic breast cancer patients receiving bevacizumab and paclitaxel as first-line chemotherapy. This study was intended to identify and validate reliable biomarkers to better predict bevacizumab treatment outcomes and allow for a more personalized use of this antiangiogenic agent. To that end, we aimed to establish risk scores for survival prognosis dichotomization based on classic clinico-pathological criteria combined or not with single nucleotide polymorphisms (SNPs). The genomic DNA of 306 patients was extracted and a panel of 13 SNPs, covering seven genes previously documented to be potentially involved in drug response, were analyzed by means of high-throughput genotyping. In receiver operating characteristic (ROC) analyses, the hazard model based on a triple-negative cancer phenotype variable, combined with specific SNPs in VEGFA (rs833061), VEGFR1 (rs9582036) and VEGFR2 (rs1870377), had the highest predictive value. The overall survival hazard ratio of patients assigned to the poor prognosis group based on this model was 3.21 (95% CI (2.33–4.42); p < 0.001). We propose that combining this pharmacogenetic approach with classical clinico-pathological characteristics could markedly improve clinical decision-making for breast cancer patients receiving bevacizumab-based therapy.

28 October 2024 in Oral Oncology
Verified
Journal Article
Closed access
AVAgathe Villarmé
Agathe Villarmé
NENathalie EBRAN
Nathalie EBRAN
TPTanguy Pacé-Loscos
Tanguy Pacé-Loscos
RSRenaud SCHIAPPA
Renaud SCHIAPPA
AMAudrey Mignot
Audrey Mignot
DCDorian Culié
Dorian Culié

15 February 2023 in Pharmaceutics
Verified
Journal Article
Open access
PDF file
JFJean-Marc antoine Ferrero
Jean-Marc antoine Ferrero
HMhakim mahammedi
hakim mahammedi
GGGwenaelle Gravis
Gwenaelle Gravis
GRGuilhem Roubaud
Guilhem Roubaud
PBPhilippe Beuzeboc
Philippe Beuzeboc
GMGérard Milano
Gérard Milano
Abiraterone acetate (AA) is the first-in-class of drugs belonging to the second-generation of agents inhibiting androgen neosynthesis in advanced prostate cancer. A cumulative experience attests that germinal gene polymorphisms may play a role in the prediction of anticancer agent pharmacodynamics variability. In the present prospective, multicentric study, gene polymorphisms of CYP17A1 (AA direct target) and the androgen transporter genes SLCO2B1 and SLCO1B3 (potential modulators of AA activity) were confronted with AA pharmacodynamics (treatment response and toxicity) in a group of 137 advanced prostate cancer patients treated in the first line by AA. The median follow-up was 56.3 months (95% CI [52.5–61]). From multivariate analysis, rs2486758 C/C (CYP17A1) and PSA (≥10 ng/mL) were associated with a shorter 3-year biological PFS (HR = 4.05, IC95% [1.46–11.22]; p = 0.007 and HR = 2.08, IC95% [1.31–3.30]; p = 0.002, respectively). From a multivariate analysis, the rs743572 (CYP17A1) and performance status were independently associated with significant toxicity (OR = 3.78 (IC95% [1.42–9.75]; p = 0.006 and OR = 4.54; IC95% [1.46–13.61]; p = 0.007, respectively). Host genome characteristics may help to predict AA treatment efficacy and identify patients at risk for toxicity.