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3 raisons identifiées
Auteur de référence en rhumatologie
26 articles scientifiques publiés — un praticien à la pointe de la recherche
Disponibilité géographique
2 lieux d'exercice — choisissez celui qui vous arrange
Délais de RDV courts dans la région
131.5 rhumatos / 100 000 hab. — département bien doté
✨ Génération du profil synthétique IA en cours…
Indicateurs publics agrégés sur 250 M+ d'œuvres scientifiques (OpenAlex, PubMed). Traduits ici en langage patient.
Influence scientifique
Données ANS publiques (Licence Ouverte 2.0) · Enrichissements MonRhumato 100 % opt-in · Toute personne référencée peut demander la suppression ou la rectification.
16
16 articles ont été cités au moins 16fois par d'autres chercheurs — preuve que ses travaux sont repris par la communauté médicale.
h-index
Total citations reçues
1 174
Nombre de fois où d'autres équipes ont mentionné ses publications dans leurs propres travaux.
Publications totales
96
Articles, revues et chapitres référencés dans les bases académiques internationales.
Articles influents
20
Publications ayant marqué leur domaine — chacune citée au moins 10 fois par d'autres chercheurs.
i10-index
Thématiques principales
Affiliations FR : Centre Hospitalier Annecy Genevois
Source : OpenAlex (CC0, OurResearch). Indicateurs académiques agrégés sur 250 M+ d'œuvres.
Articles déposés en accès libre sur l'archive ouverte des universités françaises (HAL) — gage d'activité de recherche en France.
When to stop immunotherapy for advanced melanoma: the emulated target trials
2024ArticleEClinicalMedicine
Differential gradients of immunotherapy vs targeted therapy efficacy according to the sun-exposure pattern of the site of occurrence of primary melanoma: a multicenter prospective cohort study (MelBase)
2023ArticleFrontiers in Oncology
Combined Nivolumab and Ipilimumab in Octogenarian and Nonagenarian Melanoma Patients
2023ArticleCancers
Impact of systemic therapies in metastatic melanoma of unknown primary: A study from MELBASE, a French multicentric prospective cohort
2023ArticleJournal of The American Academy of Dermatology
Non-V600E/K BRAF Mutations in Metastatic Melanoma: Molecular Description, Frequency, and Effectiveness of Targeted Therapy in a Large National Cohort
2022ArticleJCO precision oncology
Risk of irAEs in patients with autoimmune diseases treated by immune checkpoint inhibitors for stage III or IV melanoma: results from a matched case–control study
2022ArticleAnnals of the Rheumatic Diseases
Late-onset adverse events of anti-PD1 therapy in melanoma patients: An observational study from MELBASE, a nationwide prospective cohort
2022ArticleJournal of The American Academy of Dermatology
Cost-Effectiveness Analysis of Sequential Treatment Strategies for Advanced Melanoma in Real Life in France
2022ArticleCurrent Oncology
Source : HAL — archive ouverte CCSD/CNRS (couvre articles, chapitres EMC, communications congrès, thèses).
CH ANNECY-GENEVOIS SITE ANNECY
1 AV DE L'HOPITAL BP 90074, 74370 EPAGNY METZ TESSY
CABINET DU DR JULIE DE QUATREBARBES
2 TER RUE PAUL GUITON, 74000 ANNECY
Secteur de conventionnement non disponible (médecin hospitalier ou non présent dans l'Annuaire santé CNAM des libéraux conventionnés).
Lien Doctolib = recherche Google site:doctolib.fr (le 1er résultat est presque toujours le profil correct s'il existe).
Arthritis & rheumatology (Hoboken, N.J.) · 2019
ObjectiveImmune checkpoint inhibitors (ICIs) for cancer therapy frequently induce immune‐related adverse effects (IRAEs). Therefore, most patients with preexisting autoimmune diseases have been excluded from clinical trials of ICIs. This study was undertaken to evaluate the safety and efficacy of ICIs in patients with preexisting autoimmune disease and cancer.MethodsA retrospective cohort study was conducted from January 2017 to January 2018 via 3 French national networks of experts in oncology and autoimmunity. Adults with preexisting autoimmune disease who were receiving ICIs were assessed for the occurrence of flare of preexisting autoimmune disease, other IRAEs, and cancer response.ResultsThe study included 112 patients who were followed up for a median of 8 months. The most frequent preexisting autoimmune diseases were psoriasis (n = 31), rheumatoid arthritis (n = 20), and inflammatory bowel disease (n = 14). Twenty‐four patients (22%) were receiving immunosuppressive therapy at ICI initiation. Autoimmune disease flare and/or other IRAE(s) occurred in 79 patients (71%), including flare of preexisting autoimmune disease in 53 patients (47%) and/or other IRAE(s) in 47 patients (42%), with a need for immunosuppressive therapy in 48 patients (43%) and permanent discontinuation of ICI in 24 patients (21%). The median progression‐free survival was shorter in patients receiving immunosuppressive therapy at ICI initiation (3.8 months versus 12 months; P = 0.006), confirmed by multivariable analysis. The median progression‐free survival was shorter in patients who experienced a flare of preexisting autoimmune disease or other IRAE, with a trend toward better survival in the subgroup without immunosuppressant use or ICI discontinuation.ConclusionOur findings indicate that flares or IRAEs occur frequently but are mostly manageable without ICI discontinuation in patients with a preexisting autoimmune disease. Immunosuppressive therapy at baseline is associated with poorer outcomes.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2020
PURPOSETo evaluate first-line pembrolizumab monotherapy efficacy and safety in patients with unresectable cutaneous squamous cell carcinomas (CSCCs).PATIENTS AND METHODSPatients, predominantly men, with their CSSCs’ immunohistochemically determined programmed cell death-ligand 1 (PD-L1) status determined (tumor proportion score threshold, 1%), received pembrolizumab (200 mg every 3 weeks). The primary endpoint was the 39-patient primary cohort’s objective response rate at week 15 (ORRW15). Secondary objectives were best ORR, overall survival (OS), progression-free survival (PFS), duration of response (DOR), safety, ORR according to PD-L1 status and health-related quality of life using Functional Assessment of Cancer Therapy–General (FACT-G) score. An 18-patient expansion cohort, recruited to power the study to evaluate the ORRW15difference between PD-L1+ and PD-L1– patients, was assessed for ORR, disease control rate, and safety, but not survival.RESULTSMedian age of all patients was 79 years. The primary cohort’s ORRW15was 41% (95% CI, 26% to 58%), including 13 partial and 3 complete responses. Best responses were 8 partial and 8 complete responses. At a median follow-up of 22.4 months, respective median PFS, DOR, and OS were 6.7 months, not reached, and 25.3 months, respectively. Pembrolizumab-related adverse events affected 71% of the patients, and 4 (7%) were grade ≥ 3. One death was related to rapid CSCC progression; another resulted from a fatal second aggressive head and neck squamous cell carcinoma diagnosed 15 weeks postinclusion. ORRW15for the entire population was 42%; it was significantly higher for PD-L1+ patients (55%) versus PD-L1– patients (17%; P = .02). Responders’ W15 total FACT-G score had improved ( P = .025) compared with nonresponders.CONCLUSIONFirst-line pembrolizumab monotherapy exhibited promising anti-CSCC activity, with durable responses and manageable safety. PD-L1 positivity appears to be predictive of pembrolizumab efficacy.
Dermatology (Basel, Switzerland) · 2005
<i>Background:</i> Cetuximab is a member of a new family of antineoplastic agents that inhibit epidermal growth factor receptor (EGFR). These molecules may induce acneiform eruptions. In this study, we aimed at evaluating (a) the characteristics of acne and (b) whether these acneiform eruptions could be improved by classical anti-acne treatments. <i>Methods: </i>All patients treated with cetuximab in a single institution from October 2003 to May 2004 were prospectively evaluated. The presence of acne, its severity, need for a treatment and response to this treatment were recorded. <i>Results:</i> 13 patients were included: 11 (85%) developed acneiform eruptions after a mean interval of 10 days. It was severe in 4/13 (31%). Comedones were never found and acne involved nonclassical sites in 3/11. Antibiotic treatment was given to 4 and local treatment to 2 patients: it was always efficient. <i>Conclusion:</i> Cetuximab-induced acne is frequent, differs from classical acne and may be treated effectively with classical modalities.
Source PubMed · Recherche par auteur (homonymes possibles, vérifier l'affiliation).
Cancer · 2025 · Journal Article
Le Brun IC, Dalle S, Mortier L, Dereure O, et al.
EClinicalMedicine · 2024 · Journal Article
Amiot M, Mortier L, Dalle S, Dereure O, et al.
Journal of the American Academy of Dermatology · 2023 · Journal Article
Rousset P, Dalle S, Mortier L, Dereure O, et al.
Cancers · 2023 · Journal Article
Reichert C, Baldini C, Mezghani S, Maubec E, et al.
Annals of the rheumatic diseases · 2022 · Journal Article
Plaçais L, Dalle S, Dereure O, Trabelsi S, et al.
Journal of the American Academy of Dermatology · 2022 · Journal Article
Carlet C, Dalle S, Leccia MT, Mortier L, et al.
Cancers · 2021 · Journal Article
Hober C, Fredeau L, Pham-Ledard A, Boubaya M, et al.
Cancer · 2020 · Journal Article
Kandel M, Dalle S, Bardet A, Allayous C, et al.
Oncotarget · 2020 · Journal Article
Montaudié H, Viotti J, Combemale P, Dutriaux C, et al.
JAMA dermatology · 2019 · Journal Article
Vallet A, Oriano B, Mortier L, Dalle S, et al.
European journal of cancer (Oxford, England : 1990) · 2019 · Journal Article
Tétu P, Allayous C, Oriano B, Dalle S, et al.
Annales de dermatologie et de venereologie · 2016 · Comparative Study
Phan C, Sigal ML, Lhafa M, Barthélémy H, et al.
Journal of the American Academy of Dermatology · 2011 · Journal Article
Tronquoy AF, de Quatrebarbes J, Picard D, Courville P, et al.
International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2011 · Case Reports
Picard D, de Quatrebarbes J, Gueit I, Joly P
Archives of dermatology · 2005 · Clinical Trial
de Quatrebarbes J, Estève E, Bagot M, Bernard P, et al.
La Revue du praticien · 2005 · Journal Article
de Quatrebarbes J, Joly P
Dermatology (Basel, Switzerland) · 2005 · Clinical Trial, Phase II
Molinari E, De Quatrebarbes J, André T, Aractingi S
The British journal of dermatology · 2025 · Journal Article
Billard K, Mortier L, Dereure O, Dalac S, et al.
Melanoma research · 2025 · Journal Article
Macaire C, Lefevre W, Dalac S, Montaudié H, et al.
JCO precision oncology · 2022 · Multicenter Study
Girod M, Dalle S, Mortier L, Dalac S, et al.
Frontiers in oncology · 2023 · Journal Article
Russo D, Dalle S, Dereure O, Mortier L, et al.
Arthritis & rheumatology (Hoboken, N.J.) · 2019 · Evaluation Study
Tison A, Quéré G, Misery L, Funck-Brentano E, et al.
The British journal of dermatology · 2025 · Journal Article
Billard K, Mortier L, Dereure O, Dalac S, et al.
Arthritis & rheumatology (Hoboken, N.J.) · 2019 · Evaluation Study
Tison A, Quéré G, Misery L, Funck-Brentano E, et al.
Rheumatology (Oxford, England) · 2005 · Case Reports
Goëb V, Berthelot JM, Joly P, Mejjad O, et al.
British journal of cancer · 2008 · Journal Article
Lesueur F, de Lichy M, Barrois M, Durand G, et al.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2020 · Clinical Trial, Phase II
Maubec E, Boubaya M, Petrow P, Beylot-Barry M, et al.
Rheumatology (Oxford, England) · 2005 · Case Reports
Goëb V, Berthelot JM, Joly P, Mejjad O, et al.
Cancers · 2021 · Journal Article
Becquart O, Oriano B, Dalle S, Mortier L, et al.