Nadine Dohollou

ORCID: 0000-0003-2976-4090
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About
Contact & Profiles
Research Areas
  • Ovarian cancer diagnosis and treatment
  • PARP inhibition in cancer therapy
  • BRCA gene mutations in cancer
  • Radiomics and Machine Learning in Medical Imaging
  • Cancer Treatment and Pharmacology
  • Breast Cancer Treatment Studies
  • HER2/EGFR in Cancer Research
  • Advanced Breast Cancer Therapies
  • Cancer Research and Treatments
  • Economic and Financial Impacts of Cancer
  • Cancer Genomics and Diagnostics
  • Global Cancer Incidence and Screening
  • Colorectal Cancer Treatments and Studies
  • Cancer survivorship and care
  • Sarcoma Diagnosis and Treatment
  • DNA Repair Mechanisms
  • Estrogen and related hormone effects
  • Health Systems, Economic Evaluations, Quality of Life
  • Lung Cancer Treatments and Mutations
  • Endometrial and Cervical Cancer Treatments
  • Cancer Immunotherapy and Biomarkers
  • Monoclonal and Polyclonal Antibodies Research
  • Intraperitoneal and Appendiceal Malignancies
  • Renal cell carcinoma treatment
  • Phagocytosis and Immune Regulation

Polyclinique Bordeaux Nord Aquitaine
2016-2025

Polyclinique de Bordeaux-Tondu
2012-2024

Roche (Switzerland)
2021

Centre de Recherche en Cancérologie de Toulouse
2018

Clinique Pasteur
2018

Institut Bergonié
1995-2018

Inserm
2018

Institut Claudius Regaud
2018

Hôpital Tenon
2006-2017

Sorbonne Université
2006-2017

David Miles Joseph Gligorov Fabrice André David Cameron Andreas Schneeweiß and 95 more Carlos H. Barrios Binghe Xu Andrew Wardley Diego Kaen Livia Andrade Semiglazov Vf Mattea Reinisch Shilpen Patel Monika Patre L. Morales Sipahee Lal Patel M. Kaul Teresa Barata Joyce O’Shaughnessy Q. Zhang Binghe Xu Zhimin Shao Xiangyu Wang Cuizhi Geng Xingchen Yan Zhongsheng Tong Kunwei Shen Yongmei Yin Tao Sun James Chih‐Hsin Yang J. Feng Min Yan Yan Wang Qiang Liu S. Zhang Michelino De Laurentiis Armando Santoro Valentina Guarneri Marco Colleoni Clara Natoli Laura Cortesi Sabino De Placido Lorenzo Gianni Francesco Ferraù Lorenzo Livi Alberto Zambelli Lucia Del Mastro Giuseppe Tonini Filippo Montemurro Giulia Bianchi R. Pedersini Salvatore A. Del Prete Giacomo Allegrini Giuseppe Naso Patrizia Vici D. Loirat Audrey Mailliez Franck Priou Olivier Trédan F. Dalenc Christophe Perrin Joseph Gligorov M. Timar David Nadine Dohollou Luís Teixeira Fabien Brocard Antoine Arnaud Suzette Delaloge Jean‐Philippe Spano Luigi Mansi Livia Andrade Fernanda Damian José Luiz Pedrini Sandra M. Aleixo Roberto Hegg Roberto Nery Dantas Mattea Reinisch Marcus Schmidt C. Wenzel E.‐M. Grischke Andreas Schneeweiß Marianne Just Nadia Harbeck Claudia Schumacher Ubong Peters Dorothea Fischer Helmut Forstbauer Rüdiger Liersch Ellen Warner Nathaniel Bouganim C. T. Doyle Julie Price Hiller Ted Vandenberg Michel Pavic Andrew Robinson Gloria Roldan Urgoiti Nadia Califaretti Ahmet Alacacıoğlu Mahmut Gümüş Bülent Yalçın

In the phase III IMpassion130 trial, combining atezolizumab with first-line nanoparticle albumin-bound-paclitaxel for advanced triple-negative breast cancer (aTNBC) showed a statistically significant progression-free survival (PFS) benefit in intention-to-treat (ITT) and programmed death-ligand 1 (PD-L1)-positive populations, clinically meaningful overall (OS) effect PD-L1-positive aTNBC. The KEYNOTE-355 trial adding pembrolizumab to chemotherapy aTNBC similar PFS effects. IMpassion131...

10.1016/j.annonc.2021.05.801 article EN cc-by-nc-nd Annals of Oncology 2021-07-01

Deficiency in dihydropyrimidine dehydrogenase (DPD) enzyme is the main cause of severe and lethal fluoropyrimidine-related toxicity. Various approaches have been developed for DPD-deficiency screening, including DPYD genotyping phenotyping. The goal this prospective observational study was to perform exhaustive exome sequencing examine relationships between variants toxicity advanced breast cancer patients receiving capecitabine.Two-hundred forty-three were analysed (88.5% capecitabine...

10.1371/journal.pone.0175998 article EN cc-by PLoS ONE 2017-05-08

<h2>Abstract</h2><h3>Background</h3> PAOLA-1/ENGOT-ov25 (NCT02477644) demonstrated a significant progression-free survival (PFS) benefit with maintenance olaparib plus bevacizumab versus placebo in newly diagnosed, advanced ovarian cancer. We report the prespecified main second (PFS2) analysis for PAOLA-1. <h3>Methods</h3> This randomised, double-blind, phase III trial was conducted 11 countries. Eligible patients had advanced, high-grade cancer and were response after first-line...

10.1016/j.ejca.2022.07.022 article EN cc-by European Journal of Cancer 2022-09-05

Abstract Background: ESR1 mutations are known drivers of resistance to first line aromatase inhibitors (AI)-based therapy in hormone receptor-positive (HR+) HER2- metastatic breast cancer (mBC) patients (pts), but their clinical actionability remains unknown. The randomized phase 3 PADA-1 trial aimed at evaluating the benefit associated with a switch fulvestrant-palbociclib upon detection rising mutation blood (bESR1mut) HR+ mBC pts treated by AI-palbociclib.. Methods: (NCT03079011),...

10.1158/1538-7445.sabcs21-gs3-05 article EN Cancer Research 2022-02-15

PURPOSE To assess the outcome and prognosis of adults with a neoplasm related to Ewing's sarcoma family tumors. PATIENTS AND METHODS The outcomes 182 consecutive patients older than 15 years or neoplasms managed from 1982 1992 were reviewed, without any selection according primary tumor site disease extension. RESULTS Of patients, 53 had evidence metastases at presentation (29%). Tumor size was greater 10 cm in 70 (41%). With median follow-up duration 66 months, 5-year overall survival (OS)...

10.1200/jco.1998.16.12.3736 article EN Journal of Clinical Oncology 1998-12-01
Raphaël Leman Etienne Müller Angélina Legros Nicolas Goardon Imène Chentli and 95 more Alexandre Atkinson Aurore Tranchant Laurent Castéra Sophie Krieger Agathe Ricou Flavie Boulouard Florence Joly Romain Boucly Aurélie Dumont Noémie Basset Florence Coulet Louise-Marie Chevalier Étienne Rouleau Katharina Leitner Antonio González‐Martín Piera Gargiulo Hans‐Joachim Lück Catherine Genestie Gerhard Bogner Christian Marth Edgar Petru Alexander Reinthaller Christian Schauer P. Sevelda Lionel D’Hondt Ignace Vergote Peter Vuylsteke Sakari Hietanen Gabriel Lindahl Johanna Mäenpää Trine Jakobi Nøttrup Ulla Puistola Sophie Abadie‐Lacourtoisie Jérôme Alexandre Émilie Boissier Hugues Bourgeois Annick Chevalier-Place Pierre Judet de La Combe Cristina Costan Jérôme Dauba Laure De Cock Christophe Desauw Raymond Despax Nadine Dohollou Coraline Dubot Michel Fabbro Laure Favier Anne Floquet Philippe Follana Claire Garnier Tixidre Georges Garnier Laurence Gladieff Julien Grenier Cécile Guillemet Anne‐Claire Hardy‐Bessard Florence Joly Elsa Kalbacher Marie‐Christine Kaminsky Jean‐Emmanuel Kurtz Rémy Largillier Claudia Lefeuvre‐Plesse Anne Lesoin Charles-Briac Levaché Tifenn L’Haridon Alain Lortholary Jean‐Pierre Lotz Jérôme Meunier M Mousseau Marie‐Ange Mouret‐Reynier Patricia Pautier Thierry Petit Magali Provansal Éric Pujade-Lauraine Nadia Raban Isabelle Ray‐Coquard Manuel Rodrigues Frédèric Selle Robert Sverdlin Youssef Tazi Benoît You Bahriye Aktas Dirk Bauerschlag Thomas Beck Antje Belau Holger Bronger Stefan Buchholz Paul Buderath Alexander Burges Ulrich Canzler Nikolaus de Gregorio Dominik Denschlag Max Dieterich Michael Eichbaum Ayşe Balat Günter Emons

The optimal application of maintenance PARP inhibitor therapy for ovarian cancer requires accessible, robust, and rapid testing homologous recombination deficiency (HRD). However, in many countries, access to HRD is problematic the failure rate high. We developed an academic test support treatment decision-making.Genomic Instability Scar (GIScar) was through targeted sequencing a 127-gene panel determine status. GIScar trained from noninterventional study with 250 prospectively collected...

10.1158/1078-0432.ccr-23-0898 article EN cc-by-nc-nd Clinical Cancer Research 2023-09-26
Joseph Gligorov Beyhan Ataseven Mark Verrill Michelino De Laurentiis Kyung Hae Jung and 95 more Hamdy A. Azim N. Al-Sakaff Sabine Lauer Mona Shing Xavier Pivot Dhurata Koroveshi Kamel Bouzid Monica Lis Casalnuovo D. Cascallar Ernesto Korbenfeld Patricia Bastick Jane Beith Maree Colosimo Michael Friedlander Vinod Ganju Michael Green K. Patterson Andrew Redfern Gary Richardson Timur Cerić Kecman Malcic Gordana Carlos Beato M. Ferrari Roberto Hegg Vanessa Helena Gustavo Ismael Álvaro Edson Ramos Lessa Max S. Mano Alessandra Morelle Jose Alberto Lopes Nogueira K. Timcheva Antoaneta Tomova Maya Tsakova Ani Zlatareva-Petrova Jamil Asselah Hazem Assi Christine Brezden‐Masley Stephen Chia Ori Freedman Mohammed Harb Anil A. Joy Swati Kulkarni Catherine Prady Alejandro Andres Acevedo Gaete Luis Matamala Roberto Torres Eduardo Yáñez Sandra Franco Marcela Urrego Damir Gugić Damir Vrbanec Bohuslav Melichar Jana Prausová Rostislav Vyzula Rafael Gutierrez Pilarte María Isabel León René Muñoz Glenda Maria Delgado Ramos Hamdy Abdel Azeem Amr Abdel Aziz Heba El Zawahry Finlander Rosales Osegueda Jérôme Alexandre Xavier Artignan Hugues Barletta Emmanuel Beguier Jean-François Berdah C. Marty Marc A. Bollet Hugues Bourgeois C Bressac F Bürki Mario Campone David Coeffic Oana Zveltlana Cojocarasu Corinne Dagada Florence Dalenc Francesco Del Piano Christophe Desauw Isabelle Desmoulins Nadine Dohollou Joëlle Egreteau Jean-­Marc Ferrero Cyril Foa Réda Garidi Laurent Gasnault Joseph Gligorov Emmanuel Guardiola Salima Hamizi Rosana Jarcau Jean-Philippe Jacquin D Jaubert G Jolimoy H. Laharie Mineur Rémy Largillier

10.1016/j.ejca.2017.05.010 article EN European Journal of Cancer 2017-06-16

Eribulin can represent a therapeutic alternative for patients with advanced breast cancer who have received at least one or two lines of anthracyclines-based chemotherapy and taxane therapy. In this observational study, we focused on long-responder patients, i.e. an objective response stability ≥ 6 months under eribulin to better characterize them. Metastatic (MBC) treated by in 2nd, 3rd 4th line between September 2011 June-2018 were included. The following parameters assessed: primary tumor...

10.1016/j.canep.2025.102800 article EN cc-by Cancer Epidemiology 2025-03-15

Abstract Background Early access program (formerly cohort Temporary Authorization for Use) was granted trastuzumab deruxtecan (T‐DXd) in France based on DESTINY‐Breast01 trial which demonstrated its efficacy and safety HER2‐positive metastatic/unresectable breast cancer after ≥2 anti‐HER2‐based regimens received at metastatic stage. Method s This multicenter real‐world early included patients pretreated with least two lines of anti‐HER2 who T‐DXd 5.4 mg/kg intravenously monotherapy every 3...

10.1002/cam4.7168 article EN cc-by Cancer Medicine 2024-05-01

Variations in clinical response to tamoxifen (TAM) may be related polymorphic cytochromes P450 (CYPs) involved forming its active metabolite endoxifen (ENDO). We developed a population pharmacokinetic (PopPK) model for and six metabolites determine clinically relevant factors of ENDO exposure. Concentration‐time data TAM 6 come from prospective, multicenter, 3‐year follow‐up study adjuvant (20 mg/day) patients with breast cancer, plasma samples drawn every months, genotypes 63 genetic...

10.1002/cpt.2077 article EN Clinical Pharmacology & Therapeutics 2020-10-13

PURPOSE A randomized unblinded phase III trial was designed to determine the ability of granulocyte-macrophage colony-stimulating factor (GM-CSF) accelerate recovery from febrile neutropenia induced by chemotherapy. PATIENTS AND METHODS total 68 patients with following chemotherapy defined as axillary temperature greater than 38 degrees C and absolute neutrophil count (ANC) less 1 x 10(9)/L were included. After stratification for high- low-risk induce neutropenia, treatment between GM-CSF at...

10.1200/jco.1998.16.9.2930 article EN Journal of Clinical Oncology 1998-09-01

Abstract Background Ovarian cancer (OC) remains one of the most challenging and deadly malignancies facing women today. While PARP inhibitors (PARPis) have transformed treatment landscape for with advanced OC, many patients will relapse PARPi-resistant setting is an area unmet medical need. Traditional immunotherapies targeting PD-1/PD-L1 failed to show any benefit in OC. The CD47/TSP-1 axis may be relevant We aimed describe changes CD47 expression platinum therapy their relationship immune...

10.1186/s12943-024-02073-0 article EN cc-by Molecular Cancer 2024-08-14

Advanced ovarian carcinoma in early progression (<6 months) (AOCEP) is considered resistant to most cytotoxic drugs. Gemcitabine (GE) and oxaliplatin (OXA) have shown single-agent activity relapsed cancer. Their combination was tested patients with AOCEP phase II study. Fifty pre-treated platinum–taxane received q3w administration of OXA (100 mg m–2, d1) GE (1000 d1, d8, 100-min infusion). Patient characteristics were a : median age 64 years (range 46–79),and 1 (84%) or 2 (16%) earlier lines...

10.1038/sj.bjc.6604878 article EN cc-by-nc-sa British Journal of Cancer 2009-02-01

5512 Background: Nintedanib, an oral inhibitor of VEGF-FGF-PDGF receptors, has been shown to prolong progression-free survival (PFS) when added adjuvant chemotherapy after primary surgery (duBois A, Lancet Oncol 2015). CHIVA trial explored the role nintedanib in combination with NACT. Methods: Patients (pts) FIGO stage IIIC-IV chemotherapy-naive AEOC considered as unresectable laparoscopic evaluation were randomized (2:1) be treated 3 4 cycles (cy) carboplatin (AUC 5 mg/mL/min) and...

10.1200/jco.2019.37.15_suppl.5512 article EN Journal of Clinical Oncology 2019-05-20

Abstract Purpose: This study investigates changes in CD8+ cells, CD8+/Foxp3 ratio, HLA I expression, and immune coregulator density at diagnosis upon neoadjuvant chemotherapy (NACT), correlating with clinical outcomes. Experimental Design: Multiplexed profiling cell clustering analysis were performed on paired matched ovarian cancer samples to characterize the tumor microenvironment (iTME) under NACT patients enrolled CHIVA trial (NCT01583322). Results: Several (IC) subsets coregulators...

10.1158/1078-0432.ccr-23-3836 article EN cc-by-nc-nd Clinical Cancer Research 2024-04-26
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