Florent Grange

ORCID: 0000-0003-3387-0283
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About
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Research Areas
  • Cutaneous lymphoproliferative disorders research
  • Cutaneous Melanoma Detection and Management
  • Lymphoma Diagnosis and Treatment
  • Nonmelanoma Skin Cancer Studies
  • Melanoma and MAPK Pathways
  • CAR-T cell therapy research
  • Cancer Immunotherapy and Biomarkers
  • Fungal Infections and Studies
  • Cancer and Skin Lesions
  • Hedgehog Signaling Pathway Studies
  • Nail Diseases and Treatments
  • Autoimmune Bullous Skin Diseases
  • Immunotherapy and Immune Responses
  • CNS Lymphoma Diagnosis and Treatment
  • Chronic Lymphocytic Leukemia Research
  • Allergic Rhinitis and Sensitization
  • T-cell and Retrovirus Studies
  • Skin Protection and Aging
  • Protein Tyrosine Phosphatases
  • Polyomavirus and related diseases
  • Colorectal Cancer Treatments and Studies
  • melanin and skin pigmentation
  • Cancer Genomics and Diagnostics
  • Urticaria and Related Conditions
  • Coagulation, Bradykinin, Polyphosphates, and Angioedema

Centre Hospitalier de Valence
2021-2024

Université de Reims Champagne-Ardenne
2015-2024

Hôpital Robert-Debré
2014-2024

Centre Hospitalier Universitaire de Reims
2015-2024

Lymphoma Study Association
2013-2024

Inserm
1993-2023

Oxfam
2023

Liechtenstein Institute
2023

John Wiley & Sons (United States)
2023

Hudson Institute
2023

The BRAF inhibitors vemurafenib and dabrafenib have shown efficacy as monotherapies in patients with previously untreated metastatic melanoma V600E or V600K mutations. Combining the MEK inhibitor trametinib, compared alone, enhanced antitumor activity this population of patients.In open-label, phase 3 trial, we randomly assigned 704 a V600 mutation to receive either combination (150 mg twice daily) trametinib (2 once (960 orally first-line therapy. primary end point was overall survival.At...

10.1056/nejmoa1412690 article EN New England Journal of Medicine 2014-11-16

10.1016/s0140-6736(17)31266-7 article EN The Lancet 2017-06-07
Corine Bertolotto Fabienne Lesueur Sandy Giuliano Thomas Strub Mahaut de Lichy and 94 more Karine Bille Philippe Dessen Benoit d’Hayer Hamida Mohamdi Audrey Remenieras E. Maubec Arnaud de la Fouchardière Vincent Molinié P. Vabres Stéphane Dalle Nicolas Poulalhon Tanguy Martin‐Denavit L. Thomas Pascale Andry-Benzaquen N. Dupin F. Boitier Annick Rossi Jean‐Luc Perrot B. Labeille Caroline Robert Bernard Escudier Olivier Caron Laurence Brugières Simon Saule Betty Gardie Sophie Gad Richard J. Kahnoski Jérôme Couturier Bin Tean Teh Paola Ghiorzo Lorenza Pastorino Susana Puig Célia Bádenas Håkan Olsson Christian Ingvar Etienne Rouleau Rosette Lidereau Philippe Bahadoran Philippe Vielh Eve Corda Hélène Blanché Diana Zélénika Pilar Galán F. Aubin Bertrand Bachollet Céline Becuwe Pascaline Berthet Yves Jean Bignon Valérie Bonadona Jean‐Louis Bonafé Marie‐Noëlle Bonnet‐Dupeyron F. Cambazard J. Chevrant‐Breton Isabelle Coupier S. Dalac Liliane Demange M. D’Incan Catherine Dugast Laurence Faivre Lynda Vincent-Fétita Marion Gauthier-Villars Brigitte Gilbert Florent Grange Jean‐Jacques Grob Philippe Humbert Nicolas Janin Pascal Joly Delphine Kérob Christine Lasset Dominique Leroux J. Levang Jean–Marc Limacher C. Bulaï Livideanu Michel Longy Alain Lortholary Dominique Stoppa-Lyonnet S. Mansard L Mansuy Karine Marrou Christine Matéus Christine Maugard Nicolás Meyer Catherine Noguès P Souteyrand Laurence Venat‐Bouvet Hélène Zattara Valérie Chaudru Gilbert Lenoir Mark Lathrop Irwin Davidson Marie-Françoise Avril Florence Démenais Robert Ballotti Brigitte Bressac–de Paillerets

10.1038/nature10539 article EN Nature 2011-10-18

To evaluate the efficacy and safety of cetuximab, a monoclonal antibody that inhibits epidermal growth factor receptor (EGFR), as first-line monotherapy in patients with unresectable squamous cell carcinoma skin (SCCS).Thirty-six received cetuximab (initial dose 400 mg/m(2) followed by subsequent weekly doses 250 mg/m(2)) for at least 6 weeks 48-week follow-up. The primary end point was disease control rate (DCR) (according to Response Evaluation Criteria Solid Tumors [RECIST] criteria)....

10.1200/jco.2010.34.1735 article EN Journal of Clinical Oncology 2011-08-03

Therapeutic monoclonal anti-cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) antibodies are associated with immune-mediated enterocolitis. The aim of this study was to provide a detailed description entity. We included patients endoscopic signs inflammation after anti-CTLA-4 infusions for cancer treatment. Other causes enterocolitis were excluded. Clinical, biological and data recorded. A single pathologist reviewed biopsies colectomy specimens from 27 patients. Patients without...

10.1093/ecco-jcc/jjv227 article EN Journal of Crohn s and Colitis 2016-01-18
Alexander Eggermont Christian U. Blank Mario Mandalà Georgina V Long Victoria Atkinson and 95 more Stéphane Dalle Andrew Haydon Andrey Meshcheryakov Adnan Khattak Matteo S. Carlino Shahneen Sandhu James Larkin Susana Puig Paolo A. Ascierto Piotr Rutkowski Dirk Schadendorf Rutger H.T. Koornstra Leonel F. Hernandez‐Aya Anna Maria Di Giacomo Alfons J.M. van den Eertwegh Jean‐Jacques Grob Ralf Gutzmer Rahima Jamal Paul Lorigan Alexander C.J. van Akkooi Clemens Krepler Nageatte Ibrahim Sandrine Marréaud Michal Kiciński Stefan Suciu Caroline Robert Alex Menzies Thierry Lesimple Michele Maio Gerald P. Linette Michael P. Brown Peter Hersey Inge Marie Svane Laurent Mortier Jacob Schachter Catherine Barrow Ragini R. Kudchadkar Xinni Song Caroline Dutriaux Pietro Quaglino Friedegund Meier Paola Queirolo Daniil Stroyakovskiy Lars Bastholt B. Guillot Claus Garbe Pablo L. Ortiz‐Romero Florent Grange Peter Mohr Alain P. Algazi Oliver Bechter Micaela Hernberg Jean‐Philippe Arnault Philippe Saïag Carmen Loquai Frank Meiß Jan‐Christoph Simon Gil Bar‐Sela Vanna Chiarion‐Sileni Bernard M. Fitzharris Mike McCrystal Phillip Parente Jean‐François Baurain P. Combemale Célèste Lebbé Axel Hauschild Naoya Yamazaki Reinhard Dummer Mohammed Milhem Marcin Dzienis John Walker L. Geoffrois M.‐T. Leccia Lutz Kretschmer Daniel Hendler Michal Lotem Andrzej Maćkiewicz Lidija Kandolf Sekulović Elaine Dunwoodie Christoph Höeller L. Machet Jessica C. Hassel Geke A.P. Hospers Maria-Jose Passos Max Levin Martin Fehr Pippa Corrie Ashita Waterston Sigrun Hallmeyer Henrik Schmidt V. Descamps J.‐P. Lacour Carola Berking Felix Kiecker Pier Francesco Ferrucci

10.1016/s1470-2045(21)00065-6 article EN The Lancet Oncology 2021-04-14

Treatment options are limited for patients with recurrent and/or metastatic (R/M) cutaneous squamous cell carcinoma (cSCC); mortality rates exceed 70% in distant metastases. Here, we present the first interim analysis of R/M cSCC cohort from 2-cohort-locally advanced and R/M-phase II KEYNOTE-629 study.

10.1200/jco.19.03054 article EN cc-by-nc-nd Journal of Clinical Oncology 2020-07-16

PURPOSE To evaluate first-line pembrolizumab monotherapy efficacy and safety in patients with unresectable cutaneous squamous cell carcinomas (CSCCs). PATIENTS AND METHODS Patients, predominantly men, their CSSCs’ immunohistochemically determined programmed death-ligand 1 (PD-L1) status (tumor proportion score threshold, 1%), received (200 mg every 3 weeks). The primary endpoint was the 39-patient cohort’s objective response rate at week 15 (ORR W15 ). Secondary objectives were best ORR,...

10.1200/jco.19.03357 article EN Journal of Clinical Oncology 2020-07-30

Pembrolizumab demonstrated clinically meaningful and durable antitumor activity with a manageable safety profile in recurrent/metastatic (R/M) cutaneous squamous cell carcinoma (cSCC).KEYNOTE-629 was global, open-label, nonrandomized, phase II trial of patients locally advanced (LA) or R/M cSCC conducted at 59 centers. Eligible received intravenous pembrolizumab 200 mg every 3 weeks for up to 35 cycles. Primary endpoint objective response rate (ORR), defined as the percentage complete (CR)...

10.1016/j.annonc.2021.07.008 article EN cc-by-nc-nd Annals of Oncology 2021-07-20

PURPOSE: Most primary cutaneous B-cell lymphomas have an excellent prognosis. However, large (PCLBCLs) of the leg been recognized as a distinct entity with poorer prognosis in European Organization for Research and Treatment Cancer (EORTC) classification. This distinction on basis site has debated. Our aim was to identify independent prognostic factors multicenter series PCLBCL. PATIENTS AND METHODS: The clinical histologic data 145 patients PCLBCL were evaluated. According EORTC...

10.1200/jco.2001.19.16.3602 article EN Journal of Clinical Oncology 2001-08-15

To describe clinicopathologic features and to identify prognostic factors in a large series of primary cutaneous diffuse B-cell lymphoma, leg type (PCLBCL LT), as defined the recent World Health Organization-European Organization for Research Treatment Cancer classification lymphomas.Retrospective multicenter study from French Study Group on Cutaneous Lymphomas.Nineteen departments dermatology 10 regions France.Sixty patients with PCLBCL LT included registry Lymphomas.Age, sex, outcome,...

10.1001/archderm.143.9.1144 article EN Archives of Dermatology 2007-09-01

Blastic natural killer (NK) cell lymphoma (also termed CD4+CD56+ hematodermic neoplasm) is a recently described entity, with the first case reported in 1994. It was suggested initially that disease originates from NK cells. Since 1994, single cases and few small series have been published. In this review, data literature of 30 French Dutch study groups on cutaneous lymphomas are discussed. The major clinical, histopathologic, phenotypic aspects diagnostic criteria suggesting plasmacytoid...

10.1309/gjwnpd8hu5maj837 article EN American Journal of Clinical Pathology 2005-05-01

The authors report 4 cases of cutaneous lymphoproliferation unusual by their histology and clinical presentation. Each presented with a history slow growing nodule on the ear. Despite indolent evolution, suggested high-grade lymphoma. All lesions consisted dense, diffuse proliferation monomorphous medium-sized T cells throughout dermis subcutis. There was no epidermotropism grenz zone clearly present in each case. tumor displayed irregular blastlike nuclei, small nucleoli clear chromatin had...

10.1097/pas.0b013e318068b527 article EN The American Journal of Surgical Pathology 2007-11-19

Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a rare disease characterized by malignant proliferation of contingent blastic cell. This entity recognized mostly cutaneous spreading, or not having leukaemic component. The prognosis very poor.To study large cohort 90 patients with BPDCN, to define additional symptoms form correct diagnosis earlier, and manage such accordingly.We retrospectively reviewed BPDCN cases registered in the French Study Group on Cutaneous Lymphoma database...

10.1111/bjd.12412 article EN British Journal of Dermatology 2013-05-04

Journal Article Blastic plasmacytoid dendritic cell neoplasm: is transplantation the treatment of choice? Get access S. Dalle, Dalle Department Dermatology, Université Claude Bernard Lyon 1, Hospices Civils de Lyon, INSERM U590, France Stéphane Service Dermatologie, Centre Hospitalier Lyon‐Sud, 16S Cherin du Grand Revoyer, 69495 Pierre‐Bérite, France. E‐mail: stephane.dalle@chu‐lyon.fr Search for other works by this author on: Oxford Academic Google Scholar M. Beylot‐Barry, Beylot‐Barry...

10.1111/j.1365-2133.2009.09373.x article EN British Journal of Dermatology 2009-06-22

The activating mutation of MYD88 L265P is a frequent feature primary cutaneous diffuse large B-cell lymphoma, leg-type (PCLBCL-LT), reported in up to 69% the cases. Whether patients with display specific clinical and evolutive features has not been evaluated.To identify characteristics associated mutation, confirm its high prevalence, evaluate effect on prognosis PCLBCL-LT.A retrospective multicenter study was conducted using medical records from dermatology departments belonging French...

10.1001/jamadermatol.2014.821 article EN JAMA Dermatology 2014-07-23

Objective: To investigate the diagnostic value of commercially available BP230 and BP180-NC16a enzyme-linked immunosorbent assays (ELISAs) in routine practice patients with bullous pemphigoid (BP).

10.1001/archdermatol.2011.23 article EN Archives of Dermatology 2011-03-01
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