Alexandra Traverse‐Glehen

ORCID: 0000-0002-3934-0120
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About
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Research Areas
  • Lymphoma Diagnosis and Treatment
  • Chronic Lymphocytic Leukemia Research
  • Viral-associated cancers and disorders
  • Immune Cell Function and Interaction
  • CNS Lymphoma Diagnosis and Treatment
  • Monoclonal and Polyclonal Antibodies Research
  • Cancer Genomics and Diagnostics
  • T-cell and Retrovirus Studies
  • CAR-T cell therapy research
  • Cutaneous lymphoproliferative disorders research
  • Lung Cancer Treatments and Mutations
  • Cytomegalovirus and herpesvirus research
  • Breast Implant and Reconstruction
  • Cardiac tumors and thrombi
  • Diabetes and associated disorders
  • Acute Lymphoblastic Leukemia research
  • Gastrointestinal Tumor Research and Treatment
  • Cancer Immunotherapy and Biomarkers
  • Genetic factors in colorectal cancer
  • Eosinophilic Disorders and Syndromes
  • Fungal Infections and Studies
  • Cancer-related gene regulation
  • Acute Myeloid Leukemia Research
  • Chronic Myeloid Leukemia Treatments
  • T-cell and B-cell Immunology

Centre de Recherche en Cancérologie de Lyon
2016-2025

Université Claude Bernard Lyon 1
2016-2025

Hospices Civils de Lyon
2016-2025

Hôpital Lyon Sud
2016-2025

Centre National de la Recherche Scientifique
2015-2025

Inserm
2016-2025

Université de Rouen Normandie
2024

Normandie Université
2024

Centre Henri Becquerel
2024

Centre International de Recherche en Infectiologie
2022-2023

ALK-negative anaplastic large cell lymphoma associated with breast implant (i-ALCL) has been recently recognized as a distinct entity. Among 43 830 lymphomas registered in the French Lymphopath network since 2010, 300 comprising 25 peripheral T-cell (PTCL) were reviewed. PTCL, ALCL was most frequent and all of them implants.Since i-ALCL cases collected from different institutions through Lymphopath. Immuno-morphologic features, molecular data clinical outcome 19 i-ALCLs have retrospectively...

10.1093/annonc/mdv575 article EN publisher-specific-oa Annals of Oncology 2015-11-24

Purpose Although the life expectancy of patients with follicular lymphoma (FL) has increased, little is known their causes death (CODs) in rituximab era. Patients and Methods We pooled two cohorts newly diagnosed FL grade 1-3A. were enrolled between 2001 2013 French referral institutions (N = 734; median follow-up 89 months) 2002 2012 University Iowa Mayo Clinic Specialized Program Research Excellence (SPORE; N 920; 84 months). COD was classified as being a result lymphoma, other malignancy,...

10.1200/jco.18.00400 article EN Journal of Clinical Oncology 2018-11-27

Purpose To prospectively assess the clinical impact of expert review lymphoma diagnosis in France. Materials and Methods From January 2010 to December 2013, 42,145 samples from patients with newly diagnosed or suspected lymphomas were reviewed, according 2008 WHO classification, real time by experts through Lymphopath Network. Changes between referral classified as major minor their potential on patient care. Results The reviewed comprised 36,920 mature lymphomas, 321 precursor lymphoid...

10.1200/jco.2016.71.2083 article EN Journal of Clinical Oncology 2017-05-01

In recent years, overlap in biologic and morphologic features has been identified between classic Hodgkin lymphoma (cHL) B-cell non-Hodgkin lymphoma. Nevertheless, the therapeutic approaches for these diseases remain different. We undertook a study of "mediastinal gray zone lymphomas" (MGZL), with transitional cHL nodular sclerosis (NS) primary mediastinal large (MLBCL) to better understand immunophenotypic spectrum such cases. Twenty-one MGZL cases were over 20-year period. also studied 6...

10.1097/01.pas.0000180856.74572.73 article EN The American Journal of Surgical Pathology 2005-10-13

Abstract Anti‐PD‐1 therapy provides high response rates in Hodgkin lymphoma (HL) patients who have relapsed or are refractory (R/R) to autologous stem cell transplantation (ASCT) and brentuximab vedotin (BV), but median progression free survival (PFS) is only one year. The efficacy of treatment following anti‐PD‐1 not well known. We retrospectively investigated the salvage therapies for unsatisfactory therapy, assessed by PET‐CT according Lugano criteria, 30 R/R HL patients. Patients were...

10.1002/ajh.25154 article EN American Journal of Hematology 2018-06-09

Primary mediastinal B‐cell lymphoma (PMBL) is an entity of distinct from the other molecular subtypes diffuse large (DLBCL). We investigated prevalence, specificity, and clinical relevance mutations XPO1 , which encodes a member karyopherin‐β nuclear transporters, in cohort PMBL. PMBL cases defined histologically or by gene expression profiling (GEP) were sequenced mutational status was correlated to genetic characteristics. The also assessed DLBCL, Hodgkin (HL) gray‐zone (MGZL).The...

10.1002/ajh.24451 article EN American Journal of Hematology 2016-06-17
Ferdinando Bonfiglio Alessio Bruscaggin Francesca Guidetti Lodovico Terzi di Bergamo Martin Faderl and 92 more Valeria Spina Adalgisa Condoluci Luisella Bonomini Gabriela Forestieri Ricardo Koch Deborah Piffaretti Katia Pini Maria Cristina Pirosa Micol Giulia Cittone Alberto J. Arribas Marco Lucioni Guido Ghilardi Wei Wu Luca Arcaini Maria João Baptista Gabriela Bastidas Sı́lvia Beà Renzo Boldorini Alessandro Broccoli Marco Buehler Vincenzo Canzonieri Luciano Cascione Luca Ceriani Sergio Cogliatti Paolo Corradini Enrico Derenzini Liliana Devizzi Sascha Dietrich Angela Rita Elia Fabio Facchetti Gianluca Gaïdano Juan F. Garcı́a B. Gerber Paolo Ghia María Gomes da Silva Giuseppe Gritti Anna Guidetti Felicitas Hitz Giorgio Inghirami Marco Ladetto Armando López‐Guillermo Elisa Lucchini Antonino Maiorana Roberto Marasca Estella Matutes Véronique Meignin Michele Merli Alden A. Moccia Manuela Mollejo Carlos Montalbán Urban Novak David Oscier Francesco Passamonti Francesco Piazza Stefano Pizzolitto Alessandro Rambaldi Elena Sabattini Gilles Salles Elisa Santambrogio Lydia Scarfò Anastasios Stathis Georg Stüssi Julia T. Geyer Gustavo Tapia Corrado Tarella Catherine Thiéblemont Thomas Tousseyn Alessandra Tucci Giorgio Vanini Carlo Visco Umberto Vitolo Renata Walewska Francesco Zaja Thorsten Zenz Pier Luigi Zinzani Hossein Khiabanian Arianna Calcinotto Francesco Bertoni Govind Bhagat Elı́as Campo Laurence de Leval Stefan Dirnhofer Stefano Pileri Miguel Á. Piris Alexandra Traverse‐Glehen Alexandar Tzankov Marco Paulli Maurilio Ponzoni Luca Mazzucchelli Franco Cavalli Emanuele Zucca Davide Rossi

Splenic marginal zone B-cell lymphoma (SMZL) is a heterogeneous clinico-biological entity. The clinical course variable, multiple genes are mutated with no unifying mechanism, and essential regulatory pathways surrounding microenvironments diverse. We sought to clarify the heterogeneity of SMZL by resolving different subgroups their underlying genomic abnormalities, pathway signatures, microenvironment compositions uncover biomarkers therapeutic vulnerabilities. studied 303 spleen samples...

10.1182/blood.2021012386 article EN cc-by Blood 2021-10-20

Abstract Burkitt lymphoma (BL) accounts for most pediatric non-Hodgkin lymphomas, being less common but significantly more lethal when diagnosed in adults. Much of the knowledge genetics BL thus far has originated from study (pBL), leaving its relationship to adult (aBL) and other lymphomas not fully explored. We sought thoroughly identify somatic changes that underlie lymphomagenesis aBL any molecular features associate with clinical disparities within between pBL aBL. Through comprehensive...

10.1182/blood.2022016534 article EN cc-by-nc-nd Blood 2022-10-06

The prognosis of patients with early-stage unfavorable Hodgkin lymphoma remains unsatisfactory. We assessed the efficacy and safety brentuximab vedotin plus doxorubicin, vinblastine, dacarbazine (BV-AVD) in previously untreated, (ClinicalTrials.gov identifier: NCT02292979). BREACH is a multicenter, randomized, open-label, phase II trial. Eligible were age 18-60 years ≥ 1 EORTC/LYSA criterion. Patients randomly assigned (2:1) to four cycles BV-AVD or standard bleomycin, vincristine, (ABVD),...

10.1200/jco.21.01281 article EN Journal of Clinical Oncology 2022-07-22

Background Classically, splenic marginal zone B-cell lymphoma is characterized by the absence of CD5 expression. Cases apparent showing expression, as diagnosed blood studies, have been described; however, in histological evidence, correct diagnosis these cases controversial because possible confusion with other CD5-positive small neoplasms.Design and Methods We report a series 24 CD5-positive, t(11;14)-negative flow cytometry studies histologically proven on spleen sections. Clinical data...

10.3324/haematol.2009.011049 article EN cc-by-nc Haematologica 2009-12-16

Splenectomy is considered as one of the first-line treatments for symptomatic patients with splenic marginal zone lymphoma (SMZL). Between 1997 and 2012, 100 hepatitis C virus-negative SMZL were treated by splenectomy treatment. At 6 months, all but three recovered from cytopenias. The median lymphocyte count at months 1 year was 11.51 × 109/L 6.9 109/L, respectively. Median progression-free survival (PFS) 8.25 years. 5-year 10-year overall (OS) rates 84% 67%, Histological transformation...

10.3109/10428194.2013.861067 article EN Leukemia & lymphoma/Leukemia and lymphoma 2013-11-11
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