Eva González‐Barca

ORCID: 0000-0002-1323-1508
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About
Contact & Profiles
Research Areas
  • Lymphoma Diagnosis and Treatment
  • Chronic Lymphocytic Leukemia Research
  • Viral-associated cancers and disorders
  • CAR-T cell therapy research
  • CNS Lymphoma Diagnosis and Treatment
  • Acute Lymphoblastic Leukemia research
  • Cutaneous lymphoproliferative disorders research
  • Monoclonal and Polyclonal Antibodies Research
  • Immunodeficiency and Autoimmune Disorders
  • Polyomavirus and related diseases
  • T-cell and Retrovirus Studies
  • Glioma Diagnosis and Treatment
  • Lung Cancer Treatments and Mutations
  • Protein Degradation and Inhibitors
  • Immune Cell Function and Interaction
  • Neutropenia and Cancer Infections
  • Advanced Breast Cancer Therapies
  • Sarcoma Diagnosis and Treatment
  • Medical Imaging Techniques and Applications
  • Chronic Myeloid Leukemia Treatments
  • Fungal Infections and Studies
  • Multiple Myeloma Research and Treatments
  • Bacterial Identification and Susceptibility Testing
  • Glycosylation and Glycoproteins Research
  • Nail Diseases and Treatments

Institut Català d'Oncologia
2016-2025

Universitat de Barcelona
2016-2025

Institut d'Investigació Biomédica de Bellvitge
2016-2025

Duran i Reynals Hospital
2015-2024

Bellvitge University Hospital
1995-2022

Institut Català d'Ornitologia
2014-2019

European Organisation for Research and Treatment of Cancer
2018

Ajuntament de L’Hospitalet
2013-2017

Spanish Oncology Genitourinary Group
2004-2015

Johns Hopkins University
2012

MYC alterations influence the survival of patients with diffuse large B-cell lymphoma. Most studies have focused on translocations but there is little information regarding impact numerical and protein expression. We analyzed genetic expression MYC, BCL2, BCL6, MALT1 in 219 cases rearrangement occurred as sole abnormality (MYC single-hit) 3% cases, concurrent BCL2 and/or BCL6 rearrangements double/triple-hit) 4%, amplifications 2% gains 19%. single-hit, double/triple-hit amplifications, not...

10.3324/haematol.2013.086173 article EN cc-by-nc Haematologica 2013-05-28
Julia Scarisbrick Pietro Quaglino H. Miles Prince Evangelia Papadavid Emmilia Hodak and 95 more M. Bagot Octavio Servitje Emilio Berti Pablo L. Ortiz‐Romero Rudolf Stadler Aikaterini Patsatsi Robert Knobler Emmanuella Guenova Fiona Child Sean Whittaker Vasiliki Nikolaou Carlo Tomasini Iris Amitay Hadas Prag Naveh C. Ram‐Wolff Maxime Battistella Silvia Alberti Violetti R. Stranzenbach Vanessa Gargallo Cristina Muniesa Triantafyllia Κoletsa Constanze Jonak Stefanie Porkert Christina Mitteldorf Teresa Estrach Andrea Combalía Márta Marschalkó Judit Csomor Ágota Szepesi Antonio Cozzio Reinhard Dummer Nicola Pimpinelli Vieri Grandi M. Beylot‐Barry Anne Pham‐Ledard Marion Wobser Eva Geissinger Ulrike Wehkamp Michael Weichenthal Richard Cowan Eileen Parry Jeremy P. Harris Rachel Wachsmuth Deborah Turner Andrew Bates Eugene Healy Franz Trautinger Johanna Latzka Jungmin Yoo B. Vydianath Rasoul Amel-Kashipaz Leonidas Marinos A. Oikonomidi Alexander J. Stratigos Marie‐Dominique Vignon‐Pennamen Maxime Battistella Fina Climent Eva González‐Barca Elisavet Georgiou Rebecca Senetta Pier Luigi Zinzani Liisa Väkevä Annamari Ranki A.M. Busschots Esther Hauben An Bervoets F. J. Sherida H. Woei‐A‐Jin Rubeta Matin Graham P. Collins Sophie Weatherhead J. Frew M. Bayne Giles Dunnill Pam McKay Arvind Arumainathan Richard Azurdia Kim Benstead Robert Twigger Kerri E. Rieger Ryanne A. Brown José Antônio Sanches Denis Miyashiro Oleg E. Akilov Sue McCann Helka Sahi Fabiana Damasco Christiane Querfeld Amy Folkes Cecilia Bur C.‐D. Klemke Paula Enz Ramón M. Pujol Koen D. Quint Larisa J. Geskin Eric Hong

Survival in mycosis fungoides (MF) is varied and may be poor. The PROCLIPI (PROspective Cutaneous Lymphoma International Prognostic Index) study a web-based data collection system for early-stage MF with legal data-sharing agreements permitting international collaboration rare cancer complex pathology. Clinicopathological must 100% complete in-built intelligence the database ensures accurate staging.

10.1111/bjd.17258 article EN British Journal of Dermatology 2018-09-29

Tafasitamab (MOR208), an Fc-modified, humanized, anti-CD19 monoclonal antibody, combined with the immunomodulatory drug lenalidomide was clinically active a good tolerability profile in open-label, single-arm, phase II L-MIND study of patients relapsed/refractory diffuse large B-cell lymphoma (DLBCL) ineligible for autologous stem-cell transplantation. To assess long-term outcomes, we report updated analysis ≥35 months’ follow-up. Patients were aged >18 years, had received one to three...

10.3324/haematol.2020.275958 article EN cc-by-nc Haematologica 2021-07-01

Here, we evaluate the sensitivity and specificity of a new 11-parameter flow cytometry (FCM) approach versus conventional cytology (CC) for detecting neoplastic cells in stabilized CSF samples from newly diagnosed aggressive B-cell non-Hodgkin's lymphoma (B-NHL) at high risk CNS relapse, using prospective, multicentric study design.Moreover, compared distribution different subpopulations leukocytes clinico-biologic characteristics CSF+ CSF-, patients, an attempt to define algorithms useful...

10.1200/jco.2008.17.7089 article EN Journal of Clinical Oncology 2009-02-18

Background The role of re-treatment with rituximab in aggressive B-cell lymphomas still needs to be defined. This study evaluated the influence prior exposure on response rates and survival patients diffuse large lymphoma treated plus etoposide, cytarabine, cisplatinum methylprednisolone (R-ESHAP).Design Methods We retrospectively analyzed 163 relapsed or refractory who received R-ESHAP as salvage therapy a curative purpose. Patients were divided into two groups according whether had been...

10.3324/haematol.13440 article EN cc-by-nc Haematologica 2008-10-22

Genome studies of diffuse large B-cell lymphoma (DLBCL) have revealed a number somatic mutations and structural alterations. However, the clinical significance these alterations is still not well defined. In this study, we integrated analysis targeted next-generation sequencing 106 genes genomic copy (CNA) in 150 DLBCL. The clinically significant findings were validated an independent cohort 111 patients. Germinal center activated DLBCL had differential profile mutations, altered pathogenic...

10.1038/leu.2017.251 article EN cc-by-nc-nd Leukemia 2017-08-14

Background Diffuse large B-cell lymphoma is a clinically and molecularly heterogeneous disease. Gene expression profiling studies have shown that the tumor microenvironment affects survival angiogenesis-related signature prognostically unfavorable. The contribution of histopathological microvessel density to in diffuse lymphomas treated with immunochemotherapy remains unknown. purpose this study assess prognostic impact two independent series patients immunochemotherapy.Design Methods One...

10.3324/haematol.2010.037408 article EN cc-by-nc Haematologica 2011-05-05
Tadeusz Robak Jie Jin Halyna Pylypenko Gregor Verhoef Noppadol Siritanaratkul and 95 more Johannes Drach Markus Raderer Jiřı́ Mayer Juliana Pereira Gayane Tumyan Rumiko Okamoto Susumu Nakahara Peter Hu Carlos Appiani Sepideh Nemat Franco Cavalli Achiel Van Hoof Adriana Sheliga Adriana Teixeira Akihiro Tomita Albert Oriol Rocafiguera А. Н. Суворов Alexy Kuzmin Ali Khojasteh Amel Mézlini А К Голенков André Bosly Andrew R. Belch Ann Van de Velde Árpád Illes Ashis Mukhopadhyay Balkis Meddeb Bernard De Prijck Bernardo Garichochea Bülent Ündar Caballero Gabarrón Carmen Cao Cármino Antônio De Souza Charles M. Farber Cheol Won Suh C Burcoveanu C. Cebotaru Cristina-Ligia Truica Dai Maruyama David Belada Dina Ben Yehuda Dmitry Udovitsa Dolores Enrica Morra E. Späth‐Schwalbe Eva González‐Barca Evgenii A. Osmanov Francisco Capote Fritz Offner Gálvez Cárdenas Georg Heß Georgii Manikhas Govind Babu Grigoriy Rekhtman Guiseppe Rossi Herlander Marques Horia Bumbea Huaqing Wang Huiqiang Huang Ilseung Choi Irina Bulavina Irina B. Lysenko Irit Avivi Iryna Kryachok Jan Maciej Zaucha Jan Novák Joaquín Díaz Judit Demeter Julia Alexeeva Jun Zhu Kateryna Vilchevskaya Kenichi Ishizawa Kenny Mauricio Kensei Tobinai Kiyoshi Ando Kudrat Abdulkadryrov Lee‐Yung Shih Lyudmila Kuzina Mahmut Gümüş Maike de Wit Marcelo Capra Margarida Marques Marina Golubeva Mario Ojeda‐Uribe Maryna Kyselyova Masafumi Taniwaki Massimo Federico Michael Crump Michele Baccarani Michinori Ogura Miklós Egyed M. Udvardy Mitsutoshi Kurosawa Naokuni Uike Nuriet K. Khuageva

10.1016/s1470-2045(18)30685-5 article EN The Lancet Oncology 2018-10-19

The need for an individualized management of indolent clinical forms in mantle cell lymphoma (MCL) is increasingly recognized. We hypothesized that a tailored treatment with ibrutinib combination rituximab (IR) could obtain significant responses these patients.This multicenter single-arm, open-label, phase II study two-stage design conducted 12 Spanish GELTAMO sites (ClinicalTrials.gov identifier: NCT02682641). Previously untreated MCL patients defined by the following criteria were...

10.1200/jco.21.02321 article EN cc-by-nc-nd Journal of Clinical Oncology 2022-01-14

We prospectively studied 485 episodes of bacteremia in neutropenic patients with cancer. Viridans streptococci caused a total 88 (18%). Ten (11%) these cases were associated serious complications: acute respiratory distress syndrome (ARDS) plus septic shock (5 cases), ARDS (3), and (2). Streptococcus mitis was the species most frequently isolated (7 10 episodes). Four viridans showed diminished susceptibility to penicillin (MICs ranged from 0.25 4 µg/mL), 5 strains resistant ceftazidime 2...

10.1086/317460 article EN Clinical Infectious Diseases 2000-11-15

The frequency of gastrointestinal (GI) tract involvement in mantle cell lymphoma (MCL) at diagnosis is reported to be below 30%. To investigate the actual GI by MCL, upper and lower endoscopy was prospectively performed on 13 untreated MCL patients diagnosis. Multiple biopsies from endoscopically normal abnormal gastric colonic mucosa were studied with immunohistochemistry (IHC) for CD20, CD5, cyclin D1, as well fluorescence situ hybridization (FISH) t(11;14) polymerase chain reaction (PCR)...

10.1097/01.pas.0000208899.15859.cb article EN The American Journal of Surgical Pathology 2006-09-12

The elective treatment of patients with post-transplant lymphoproliferative disorders is controversial. purpose this trial was to evaluate the efficacy extended doses rituximab adapted response in after solid organ transplantation.This a prospective, multicenter, phase II trial. Patients were treated reduction immunosuppression and four weekly infusions rituximab. Those who did not achieve complete remission (CR) received second course infusions. primary end-point study CR rate.Thirty-eight...

10.3324/haematol.11360 article EN cc-by-nc Haematologica 2007-10-31

The addition of monoclonal antibodies to chemotherapy has significantly improved treatment chronic lymphocytic leukemia (CLL). Based on excellent results with the chemotherapy-only regimen fludarabine, cyclophosphamide, and mitoxantrone (FCM), we built a new chemoimmunotherapy combination--rituximab plus FCM (R-FCM). We report phase II clinical trial consisting an initial R-FCM followed by rituximab maintenance.Seventy-two untreated CLL patients age 70 years or younger received 500 mg/m(2)...

10.1200/jco.2009.22.0442 article EN Journal of Clinical Oncology 2009-08-25

Fludarabine, cyclophosphamide, and mitoxantrone (FCM) results in a high response rate previously treated patients with chronic lymphocytic leukemia (CLL). The aim of this study was to investigate FCM as frontline therapy CLL.Sixty-nine under the age 65 years active CLL were treated. Patients received six cycles fludarabine 25 mg/m(2) i.v. x 3 days, cyclophosphamide 200 6 1 day. Treatment outcome correlated clinical biological variables. significance eradicating minimal residual disease (MRD)...

10.1158/1078-0432.ccr-07-1371 article EN Clinical Cancer Research 2008-01-01

Summary Immunochemotherapy with cyclophosphamide, adriamycin, vincristine, prednisone and rituximab (R‐CHOP) is the standard treatment in non‐immunosuppressed patients diffuse large B‐cell lymphoma (DLBCL), but its adequacy has not been definitively established human immunodeficiency virus (HIV)‐related lymphoma. This phase II trial aimed to evaluate safety efficacy of six cycles R‐CHOP HIV‐related DLBCL determine whether response highly active antiretroviral therapy (HAART) had prognostic...

10.1111/j.1365-2141.2007.06943.x article EN British Journal of Haematology 2007-12-20

// Lourdes Martín-Martín 1 , Julia Almeida Helena Pomares 2 Eva González-Barca Pilar Bravo 3 Teresa Giménez 4 Cecilia Heras 5 José-Antonio Queizán 6 Elena Pérez-Ceballos 7 Violeta Martínez 8 Natalia Alonso 9 Carlota Calvo 10 Rodolfo Álvarez 11 María Dolores Caballero 12 and Alberto Orfao Cancer Research Centre (IBMCC, USAL-CSIC), Institute for Biomedical of Salamanca (IBSAL) Department Medicine Cytometry Service (NUCLEUS Support Platform), University (USAL), Salamanca, Spain Hematology...

10.18632/oncotarget.7101 article EN Oncotarget 2016-01-31

The benefit of intrathecal therapy and systemic rituximab on the outcome diffuse large B-cell lymphoma at risk central nervous system disease is controversial. Furthermore, effect treatment in Burkitt with occult leptomeningeal detected by flow cytometry diagnosis unknown. Untreated (n=246) (n=80) clinical having had pre-treatment cerebrospinal fluid were analyzed cytology. Spinal involvement was alone (occult) 33 (13%) 9 (11%) patients, cytology 11 (4.5%) 5 (6%) respectively. Diffuse spinal...

10.3324/haematol.2013.101741 article EN cc-by-nc Haematologica 2014-04-11

Abstract Mantle cell lymphoma (MCL) is a mature B‐cell neoplasm with an aggressive behavior, characterized by the t(11;14)(q13;q32). Several secondary genetic abnormalities potential role in oncogenic process have been described. Studies of large MCL series using conventional cytogenetics, and correlating proliferation survival, are scarce. We selected 145 cases at diagnosis, displaying aberrant karyotype, from centers belonging to Spanish Cooperative Group for Hematological Cytogenetics....

10.1002/gcc.20754 article EN Genes Chromosomes and Cancer 2010-02-08
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