Laurence Sanhès

ORCID: 0000-0003-1207-7665
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Research Areas
  • Acute Myeloid Leukemia Research
  • Lymphoma Diagnosis and Treatment
  • Multiple Myeloma Research and Treatments
  • Chronic Lymphocytic Leukemia Research
  • Acute Lymphoblastic Leukemia research
  • Myeloproliferative Neoplasms: Diagnosis and Treatment
  • Protein Degradation and Inhibitors
  • Chronic Myeloid Leukemia Treatments
  • CNS Lymphoma Diagnosis and Treatment
  • Viral-associated cancers and disorders
  • T-cell and Retrovirus Studies
  • Cutaneous lymphoproliferative disorders research
  • Neutropenia and Cancer Infections
  • Hematological disorders and diagnostics
  • Immunodeficiency and Autoimmune Disorders
  • Histone Deacetylase Inhibitors Research
  • Hemoglobinopathies and Related Disorders
  • Glioma Diagnosis and Treatment
  • Hematopoietic Stem Cell Transplantation
  • Occupational and environmental lung diseases
  • Advanced Breast Cancer Therapies
  • Cancer Treatment and Pharmacology
  • PI3K/AKT/mTOR signaling in cancer
  • CAR-T cell therapy research
  • Pneumocystis jirovecii pneumonia detection and treatment

Centre Hospitalier de Perpignan
2016-2025

Groupe Francophone des Myélodysplasies
2004-2019

Recherche clinique appliquée à l'hématologie
2018

Assistance Publique – Hôpitaux de Paris
2003-2018

Hôpital Saint-Louis
2016-2018

Université Paris Cité
2016-2018

Délégation Paris 7
2016

Inserm
2003-2012

Institut pour l'avancée des biosciences
2012

Centre Hospitalier Universitaire de Tours
2012

The long-term prognosis for older patients with mantle-cell lymphoma is poor. Chemoimmunotherapy results in low rates of complete remission, and most have a relapse. We investigated whether fludarabine-containing induction regimen improved the complete-remission rate maintenance therapy rituximab prolonged remission.We randomly assigned 60 years age or lymphoma, stage II to IV, who were not eligible high-dose six cycles rituximab, fludarabine, cyclophosphamide (R-FC) every 28 days eight...

10.1056/nejmoa1200920 article EN New England Journal of Medicine 2012-08-08

To determine the efficacy and toxicity of chemoimmunotherapy followed by either whole-brain radiotherapy (WBRT) or intensive chemotherapy autologous stem-cell transplantation (ASCT) as a first-line treatment primary CNS lymphoma (PCNSL).Immunocompetent patients (18 to 60 years age) with untreated PCNSL were randomly assigned receive WBRT ASCT consolidation after induction consisting two cycles R-MBVP (rituximab 375 mg/m2 day (D) 1, methotrexate 3 g/m2 D1; D15, VP16 100 D2, BCNU D3,...

10.1200/jco.18.00306 article EN Journal of Clinical Oncology 2019-02-20

To determine the efficacy and safety of bendamustine as a single agent in refractory or relapsed T-cell lymphomas.Patients with histologically confirmed peripheral lymphoma (PTCL) cutaneous who progressed after one more lines prior chemotherapy received at 120 mg/m(2) per day on days 1 through 2 every 3 weeks for six cycles. The primary end point was overall response rate (ORR). Secondary points were duration (DOR), progression-free survival (PFS), (OS).Of 60 patients included, 27 (45%) to...

10.1200/jco.2012.43.7285 article EN Journal of Clinical Oncology 2012-10-30

Background. Good syndrome (GS) is a rare condition in which thymoma associated with hypogammaglobulinemia. It characterized by increased susceptibility to bacterial, viral, and fungal infections, as well autoimmunity. Most patients have no circulating B cells.

10.1093/cid/civ269 article EN Clinical Infectious Diseases 2015-03-31

Clinical trials frequently include multiple end points that mature at different times. The initial report, typically based on the primary point, may be published when key planned co-primary or secondary analyses are not yet available. Trial Updates provide an opportunity to disseminate additional results from studies, in JCO elsewhere, for which point has already been reported.We previously reported of a randomized phase II study patients with newly diagnosed CNS lymphoma (age 18-60 years)....

10.1200/jco.22.00491 article EN Journal of Clinical Oncology 2022-07-14

SummaryBackgroundIn our previous study on erythropoiesis-stimulating agent (ESA) treatment in lower risk myelodysplastic syndromes from the European MDS (EUMDS) Registry, we showed that patients treated with ESAs had longer survival compared who receive red blood cell transfusion (RBCT). In this study, a follow up time and more included, aimed to assess long-term effects health-related quality of life (HRQoL) exposure or without RBCT syndromes.MethodsThe EUMDS Registry is non-interventional,...

10.1016/s2352-3026(24)00350-8 article EN cc-by The Lancet Haematology 2025-02-01

Summary Baseline characteristics, disease‐management and outcome of 1000 lower‐risk myelodysplastic syndrome ( MDS ) patients within the European LeukaemiaNet EUMDS Registry are described in conjunction with validation revised International Prognostic Scoring System IPSS ‐R). The registry confirmed established prognostic factors, such as age, gender World Health Organization 2001 classification. Low quality life EQ ‐5D visual analogue scale score) was significantly associated reduced...

10.1111/bjh.13450 article EN British Journal of Haematology 2015-04-24
Sophie Vaux Alexis Criscuolo Marie Desnos-Ollivier Laure Diancourt Chloé Tarnaud and 95 more Mathias Vandenbogaert Sylvain Brisse B. Coignard Françoise Dromer Dea García-Hermoso Catherine Blanc Damien Hoinard Olivier Lortholary Stéphane Bretagne Jean‐Michel Thiolet Henriette de Valk Rémi Courbil A. Chabanel Marion Simonet Françoise Maire S. Jbilou Pierre Tiberghien Hervé Blanchard Anne-Gaëlle Venier C. Bernet Loïc Simon Hélène Sénéchal Élodie Pouchol Christiane Angot Patricia Ribaud Gérard Socié M. Flèche Nathalie Brieu E. Lagier Vanessa Chartier Thierry Allègre Laurence Maulin Hélène Lanic Hervé Tilly Jean‐Philippe Bouchara Marc Pihet Aline Schmidt Achille Kouatchet Yves-Marie Vandamme Norbert Ifrah Alain Mercat Isabelle Accoceberry Olivier Albert Thibaut Leguay Anne-Marie Rogues Julie Bonhomme Oumédaly Reman Claire Lesteven Philippe Poirier Cécile Moluçon‐Chabrot Laure Calvet Olivier Baud Monique Cambon Jean Chistophe Farkas Bruno Lafon Frédéric Dalle Denis Caillot Aline Lazzarotti Serge Aho Sandrine Combret Thierry Façon Boualem Sendid Séverine Loridant Terriou Louis Bruno Cazin Bruno Grandbastien Nathalie Bourgeois Anne Lotthé Guillaume Cartron Christophe Ravel P Colson Philippe Gaudard Caroline Bonmati Loïc Simon Christian Rabaud M. Machouart D.M. Poisson Diana Carp Jérôme Meunier Anne Gaschet Chantal Miquel Laurence Sanhès Milagros Ferreyra Franck Leibinger Philippe Geudet D. Toubas Chantal Himberlin Florence Bureau-Chalot Alain Delmer Loïc Favennec Gilles Gargala Jean‐Marie Michot Christophe Girault Marion David Stéphane Leprêtre

ABSTRACT Rapidly fatal cases of invasive fungal infections due to a fungus later identified as Saprochaete clavata were reported in France May 2012. The objectives this study determine the clonal relatedness isolates and investigate possible sources contamination. A nationwide alert was launched collect cases. Molecular identification methods, whole-genome sequencing (WGS), clone-specific genotyping used analyze recent historical isolates, case-case performed. Isolates from thirty (26...

10.1128/mbio.02309-14 article EN cc-by-nc-sa mBio 2014-12-17

The GRASPALL/GRAALL-SA2-2008 Phase II trial evaluated the safety and efficacy of L-asparaginase encapsulated within erythrocytes (GRASPA®) in patients ≥ 55 years with Philadelphia chromosome-negative acute lymphoblastic leukemia.Thirty received escalating doses GRASPA® on Day 3 6 induction Phases 1 2. primary endpoint was asparagine depletion < 2 µmol/L for at least 7 days. This reached 85 71% 100 150 IU/kg respectively but not 50 IU/kg. Grade 3/4 infection, hypertransaminasemia,...

10.1002/ajh.24093 article EN American Journal of Hematology 2015-06-20
Mohamad Mohty Evangelos Terpos María‐Victoria Mateos Michèle Cavo Sandra Lejniece and 95 more Meral Beksaç Mohamed Amine Bekadja Wojciech Legieć Meletios Α. Dimopoulos Svetlana Stankovic María Soledad Durán Valerio De Stefano Alessandro Corso Yulia Kochkareva Edward Laane Christian Berthou Hans Salwender Zvenyslava Masliak Valdas Pečeliūnas Wolfgang Willenbacher João Pedro Silva Vernon Louw Damir Nemet Zita Borbényi Uri Abadi Robert Schou Pedersen Peter Černelč Anna Potamianou Catherine Couturier Caroline Feys Florence Thoret-Bauchet Mario Boccadoro Mohamed Amine Bekadja Rose‐Marie Hamladji Hocine Ait Ali Selma Hamdi Hadj Touhami Nourredine Sidi Mansour Wolfgang Willenbacher Werner Linkesch Damir Nemet Robert S. Pedersen Niels Abildgaard Edward Laane Marju Hein Mohamad Mohty Jean Richard Eveillard Abderrazak El Yamani Philippe Moreau Laurence Sanhès G. Lepeu Kamel Laribi Éric Jourdan Olivier Fitoussi Olivier Allangba Joël Fleury Martine Escoffre Riad Benramdane Guillaume Cartron Gérard Dine Eric Legouffe Hanns‐Detlev Harich Thomas Illmer Steffen Dörfel Carla Hannig Michael Koenigsmann Gabriele Prange‐Krex Hans Salwender Ingo Tamm W. Zeller M. Maasberg Rudolf Schlag Martine Klausmann Jens Uhlig Burkhard Alkemper Stefan Schütz Hans-Werner Tessen Benno Mohr Peter Schmidt Bernhard Heinrich Holger Hebart G. Seipelt Thomas Zoeller Frank Heits C. Müller-Naendrup Richard Hansen Roland Repp Ludwig Fischer von Weikersthal Rudolf Schmits Jörg Heßling B. Krammer-Steiner Viktor Janzen Michael Schauer M Grüner Jens Kisro Claudio Denzlinger W. Freier Christian Junghanß Martin Görner Katharina Laichinger

BackgroundThe present prospective, multinational, noninterventional study aimed to document and describe real-world treatment regimens disease progression in multiple myeloma (MM) patients.Patients MethodsAdult patients initiating any new MM therapy from October 2010 2012 were eligible. A multistage patient/site recruitment model was applied minimize the selection bias; enrollment stratified by country, region, practice type. The patient medical features, history, remission status recorded...

10.1016/j.clml.2018.06.018 article EN cc-by-nc-nd Clinical Lymphoma Myeloma & Leukemia 2018-06-25

Abstract Despite very similar gene expression profiles, the clinical course of B-cell chronic lymphocytic leukemia (B-CLL) is heterogeneous. Immunoglobulin VH (IgVH) mutational status and receptor (BCR) signaling mediators have been associated with disease progression. However, consequences BCR engagement on cell survival evolution remain unclear. We show here that B-CLL dependent threshold stimulation induced by immobilized antibody, in contrast to soluble anti-μ F(ab)′2 which leads...

10.1158/0008-5472.can-06-0085 article EN Cancer Research 2006-07-15

The efficacy of azacitidine in patients with anemia and lower-risk myelodysplastic syndromes, if relapsing after or resistant to erythropoietic stimulating agents, the benefit combining these agents this setting are not well known. We prospectively compared outcomes patients, all them having characteristics subset syndrome, randomly treated alone combined epoetin-β. High-resolution cytogenetics gene mutation analysis were performed at entry. primary study endpoint was achievement red blood...

10.3324/haematol.2015.140988 article EN cc-by-nc Haematologica 2016-05-26

Central nervous system (CNS) thrombotic events are a well-known complication of acute lymphoblastic leukemia (ALL) induction therapy, especially with treatments including l-asparaginase (l-ASP). Data on risk factors and clinical evolution is still lacking in adult patients. We report the 22 CNS venous thrombosis cases occurring 708 adults treated for ALL or lymphoma (LL) Group Research Adult Acute Lymphoblastic Leukemia (GRAALL)-induction protocol, which included eight L-ASP (6,000 IU/m(2) )...

10.1002/ajh.24130 article EN American Journal of Hematology 2015-07-27

Quantification of minimal residual disease may guide therapeutic strategies in mantle cell lymphoma. While multiparameter flow cytometry is used for diagnosis, the gold standard method analysis real-time quantitative polymerase chain reaction (RQ-PCR). In this European Mantle Cell Lymphoma network (EU-MCL) pilot study, we compared with RQ-PCR detection. Of 113 patients at least one sample, was applicable 97 (86%). A total 284 samples from 61 were analyzed parallel by and RQ-PCR. single,...

10.3324/haematol.2015.134957 article EN cc-by-nc Haematologica 2015-12-24

High-risk myelodysplastic syndrome/acute myeloid leukemia patients have a very poor survival after azacitidine failure. Guadecitabine (SGI-110) is novel subcutaneous hypomethylating agent which results in extended decitabine exposure. This multicenter phase II study evaluated the efficacy and safety of guadecitabine high-risk syndrome low blast count acute refractory or relapsing azacitidine. We included 56 with median age 75 years [Interquartile Range (IQR) 69-76]. Fifty-five received at...

10.3324/haematol.2018.207118 article EN cc-by-nc Haematologica 2019-02-07

Rituximab improves progression-free survival (PFS) and time to next treatment (TTNT) when compared with the watch wait strategy for patients low-tumor burden follicular lymphoma (FL). Prolonged rituximab maintenance did not prolong TTNT, whereas it raises concerns about resources use patient adhesion. Our aim was then investigate of short using subcutaneous (SC) route in FL.Patients histologically confirmed CD20+ FL were randomly assigned receive either rituximab, 375 mg/m2 once daily on D1,...

10.1200/jco.22.02327 article EN Journal of Clinical Oncology 2023-04-18
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