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Auteur de référence en rhumatologie
20 articles scientifiques publiés — un praticien à la pointe de la recherche
Référence presse grand public
Cité 2 fois dans les médias — pédagogie reconnue
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Délais de RDV courts dans la région
336.2 rhumatos / 100 000 hab. — département bien doté
✨ Génération du profil synthétique IA en cours…
Articles déposés en accès libre sur l'archive ouverte des universités françaises (HAL) — gage d'activité de recherche en France.
Données ANS publiques (Licence Ouverte 2.0) · Enrichissements MonRhumato 100 % opt-in · Toute personne référencée peut demander la suppression ou la rectification.
Source : HAL — archive ouverte CCSD/CNRS (couvre articles, chapitres EMC, communications congrès, thèses).
HOPITAL FONDATION A DE ROTHSCHILD
25 R MANIN, 75019 PARIS
CABINET DU DR MARC SPIELMANN
17 RUE PETRARQUE, 75016 PARIS
INSTITUT GUSTAVE ROUSSY
39 B R CAMILLE DESMOULINS, 94805 VILLEJUIF CEDEX
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).
Source : Google News (recherche par nom complet — homonymes possibles, vérifier le contenu).
📰 Capital.fr · 26/11/2013
<a href="https://news.google.com/rss/articles/CBMioAFBVV95cUxQOThPLUtYcFo1ZlpETzhHYlVsXzB4Y3ZKZGVFYXhEVmNFbU5PNjhuTkM5VnhkUWxIQjV0SzdscG8teXA0MEVXdWxadUlkMFJBUkhpTktRbVdsVDEzRFlRY2pBQXlTaGdpSmEzWWlKZWJRX3VlbFhBZlNvQzE2MHJ3OEJ4OWhFUUZrLVJHRzFSY1BlWi1VZ2VOUlEzM05va0V3?oc=5" target="_blank">Nos médecin
📰 parismatch.com · 28/05/2013
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Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2006
Purpose The PACS 01 trial compared six cycles of fluorouracil, epirubicin, and cyclophosphamide (FEC) with a sequential regimen of three cycles of FEC followed by three cycles of docetaxel (FEC-D) as adjuvant treatment for women with node-positive early breast cancer. Patients and Methods Between June 1997 and March 2000, 1,999 patients with operable node-positive breast cancer were randomly assigned to either FEC every 21 days for six cycles, or three cycles of FEC followed by three cycles of docetaxel, both given every 21 days. Hormone-receptor–positive patients received tamoxifen for 5 years after chemotherapy. The primary end point was 5-year disease-free survival (DFS). Results Median follow-up was 60 months. Five-year DFS rates were 73.2% with FEC and 78.4% with FEC-D (unadjusted P = .011; adjusted P = .012). Multivariate analysis adjusted for prognostic factors showed an 18% reduction in the relative risk of relapse with FEC-D. Five-year overall survival rates were 86.7% with FEC and 90.7% with FEC-D, demonstrating a 27% reduction in the relative risk of death (unadjusted P = .014; adjusted P = .017). The incidence of grade 3 to 4 neutropenia, the need for hematopoietic growth factor, and incidence of nausea/vomiting were higher with FEC. Docetaxel was associated with more febrile neutropenia in the fourth cycle, stomatitis, edema, and nail disorders. Though rare overall, there were fewer cardiac events after FEC-D (P = .03), attributable mainly to the lower anthracycline cumulative dose. Conclusion Sequential adjuvant chemotherapy with FEC followed by docetaxel significantly improves disease-free and overall survival in node-positive breast cancer patients and has a favorable safety profile.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2009
Purpose To evaluate the efficacy of trastuzumab in patients with node-positive breast cancer treated with surgery, adjuvant chemotherapy, radiotherapy, and hormone therapy if applicable. Patients and Methods Three thousand ten patients with operable node-positive breast cancer were randomly assigned to receive adjuvant anthracycline-based chemotherapy with or without docetaxel. Patients who presented human epidermal growth factor receptor 2 (HER2) -overexpressing tumors were secondary randomly assigned to either a sequential regimen of trastuzumab (6 mg/kg every 3 weeks) for 1 year or observation. The primary end point was disease-free survival (DFS). Results Overall 528 patients were randomly assigned between trastuzumab (n = 260) and observation (n = 268) arm. Of the 234 patients (90%) who received at least one administration of trastuzumab, 196 (84%) received at least 6 months of treatment, and 41 (18%) discontinued treatment due to cardiac events (any grade). At the date of analysis (October 2007), 129 DFS events were recorded. Random assignment to the trastuzumab arm was associated with a nonsignificant 14% reduction in the risk of relapse (hazard ratio, 0.86; 95% CI, 0.61 to 1.22; P = .41, log-rank stratified on pathologic node involvement). Three-year DFS rates were 78% (95% CI, 72.3 to 82.5) and 81% (95% CI, 75.3 to 85.4) in the observation and trastuzumab arms, respectively. Conclusion After a 47-month median follow-up, 1 year of trastuzumab given sequentially after adjuvant chemotherapy was not associated with a statistically significant decrease in the risk of relapse.
Breast cancer research and treatment · 2012
Source PubMed · Recherche par auteur (homonymes possibles, vérifier l'affiliation).
Future oncology (London, England) · 2015 · Clinical Trial, Phase III
Guiu S, Charon-Barra C, Vernerey D, Fumoleau P, et al.
Breast cancer research and treatment · 2013 · Clinical Trial
Roca L, Diéras V, Roché H, Lappartient E, et al.
The oncologist · 2012 · Clinical Trial, Phase III
Coudert B, Asselain B, Campone M, Spielmann M, et al.
Radiation oncology (London, England) · 2009 · Journal Article
Dzhugashvili M, Tournay E, Pichenot C, Dunant A, et al.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2009 · Journal Article
Spielmann M, Roché H, Delozier T, Canon JL, et al.
Cancer · 2009 · Journal Article
Largillier R, Savignoni A, Gligorov J, Chollet P, et al.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2006 · Journal Article
Roché H, Fumoleau P, Spielmann M, Canon JL, et al.
Clinical breast cancer · 2005 · Journal Article
Lê MG, Arriagada R, Contesso G, Cammoun M, et al.
European journal of cancer (Oxford, England : 1990) · 2018 · Clinical Trial, Phase III
Campone M, Lacroix-Triki M, Roca L, Spielmann M, et al.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2015 · Journal Article
O'Sullivan CC, Bradbury I, Campbell C, Spielmann M, et al.
Breast cancer research and treatment · 2010 · Clinical Trial, Phase II
Pierga JY, Delaloge S, Espié M, Brain E, et al.
European journal of cancer (Oxford, England : 1990) · 2011 · Journal Article
Mir O, Domont J, Cioffi A, Bonvalot S, et al.
European journal of human genetics : EJHG · 2018 · Journal Article
Pujol P, Vande Perre P, Faivre L, Sanlaville D, et al.
European journal of cancer (Oxford, England : 1990) · 2011 · Journal Article
Mir O, Domont J, Cioffi A, Bonvalot S, et al.
Critical reviews in oncology/hematology · 2009 · Journal Article
Tubiana-Hulin M, Spielmann M, Roux C, Campone M, et al.
Breast cancer (Dove Medical Press) · 2013 · Journal Article
Kader YA, Spielmann M, El-Nahas T, Sakr A, et al.
Bulletin du cancer · 2011 · Consensus Statement
Penault-Llorca F, Coeffic D, Delozier T, Dohollou N, et al.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2015 · Journal Article
O'Sullivan CC, Bradbury I, Campbell C, Spielmann M, et al.
Breast cancer research and treatment · 2012 · Journal Article
Luporsi E, André F, Spyratos F, Martin PM, et al.
Combined evaluation of LC3B puncta and HMGB1 expression predicts residual risk of relapse after adjuvant chemotherapy in breast cancer
Combined evaluation of LC3B puncta and HMGB1 expression predicts residual risk of relapse after adjuvant chemotherapy in breast cancer
Combined evaluation of LC3B puncta and HMGB1 expression predicts residual risk of relapse after adjuvant chemotherapy in breast cancer
In spite of adjuvant chemotherapy, a significant fraction of patients with localized breast cancer (BC) relapse after optimal treatment. We determined the occurrence of cytoplasmic MAP1LC3B/LC3B (microtubule-associated p
Combined evaluation of LC3B puncta and HMGB1 expression predicts residual risk of relapse after adjuvant chemotherapy in breast cancer
In spite of adjuvant chemotherapy, a significant fraction of patients with localized breast cancer (BC) relapse after optimal treatment. We determined the occurrence of cytoplasmic MAP1LC3B/LC3B (microtubule-associated p
Combined evaluation of LC3B puncta and HMGB1 expression predicts residual risk of relapse after adjuvant chemotherapy in breast cancer
In spite of adjuvant chemotherapy, a significant fraction of patients with localized breast cancer (BC) relapse after optimal treatment. We determined the occurrence of cytoplasmic MAP1LC3B/LC3B (microtubule-associated p
Combined evaluation of lc3b puncta and hmgb1 expression predicts residual risk of relapse after adjuvant chemotherapy in breast cancer
ABSTRACTIn spite of adjuvant chemotherapy, a significant fraction of patients with localized breast cancer (BC) relapse after optimal treatment. We determined the occurrence of cytoplasmic MAP1LC3B/LC3B (microtubule-asso
Source : DataCite — DOIs pour datasets, logiciels, protocoles, registres patient. Hors articles (déjà couverts).
European journal of cancer (Oxford, England : 1990) · 2014 · Journal Article
Ladoire S, Dalban C, Roché H, Spielmann M, et al.
Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology · 2012 · Clinical Trial, Phase II
Azoury F, Heymann S, Acevedo C, Spielmann M, et al.
Breast cancer research and treatment · 2010 · Clinical Trial, Phase II
Pierga JY, Delaloge S, Espié M, Brain E, et al.
Acta oncologica (Stockholm, Sweden) · 2005 · Journal Article
Arriagada R, Spielmann M, Koscielny S, Le Chevalier T, et al.