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Not all IGHV3-21 chronic lymphocytic leukemias are equal: prognostic considerations.
Baliakas, Panagiotis; Agathangelidis, Andreas; Hadzidimitriou, Anastasia; Sutton, Lesley-Ann; Minga, Eva; Tsanousa, Athina; Scarfò, Lydia; Davis, Zadie; Yan, Xiao-Jie; Shanafelt, Tait; Plevova, Karla; Sandberg, Yorick; Vojdeman, Fie Juhl; Boudjogra, Myriam; Tzenou, Tatiana; Chatzouli, Maria; Chu, Charles C; Veronese, Silvio; Gardiner, Anne; Mansouri, Larry; Smedby, Karin E; Pedersen, Lone Bredo; Moreno, Denis; Van Lom, Kirsten; Giudicelli, Véronique; Francova, Hana Skuhrova; Nguyen-Khac, Florence; Panagiotidis, Panagiotis; Juliusson, Gunnar; Angelis, Lefteris; Anagnostopoulos, Achilles; Lefranc, Marie-Paule; Facco, Monica; Trentin, Livio; Catherwood, Mark; Montillo, Marco; Geisler, Christian H; Langerak, Anton W; Pospisilova, Sarka; Chiorazzi, Nicholas; Oscier, David; Jelinek, Diane F; Darzentas, Nikos; Belessi, Chrysoula; Davi, Frederic; Ghia, Paolo; Rosenquist, Richard; Stamatopoulos, Kostas.
Afiliação
  • Baliakas P; Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden;
  • Agathangelidis A; Università Vita-Salute San Raffaele, Milan, Italy; Division of Molecular Oncology and Department of Onco-Hematology, Istituto di Ricovero e Cura a Carattere Scientifico, San Raffaele Scientific Institute, Milan, Italy;
  • Hadzidimitriou A; Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden; Institute of Applied Biosciences, Centre for Research and Technology-Hellas, Thessaloniki, Greece;
  • Sutton LA; Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden;
  • Minga E; Institute of Applied Biosciences, Centre for Research and Technology-Hellas, Thessaloniki, Greece;
  • Tsanousa A; Department of Informatics, Aristotle University of Thessaloniki, Thessaloniki, Greece;
  • Scarfò L; Università Vita-Salute San Raffaele, Milan, Italy; Division of Molecular Oncology and Department of Onco-Hematology, Istituto di Ricovero e Cura a Carattere Scientifico, San Raffaele Scientific Institute, Milan, Italy;
  • Davis Z; Department of Haematology, Royal Bournemouth Hospital, Bournemouth, United Kingdom;
  • Yan XJ; The Feinstein Institute for Medical Research, North Shore-Long Island Jewish Health System, Manhasset, NY;
  • Shanafelt T; Division of Hematology, Department of Medicine, Mayo Clinic, Rochester, MN;
  • Plevova K; Central European Institute of Technology, Masaryk University and University Hospital Brno, Brno, Czech Republic;
  • Sandberg Y; Department of Immunology, Erasmus Medical Center, University Medical Center Rotterdam, Rotterdam, The Netherlands;
  • Vojdeman FJ; Department of Hematology, Rigshospitalet, Copenhagen, Denmark;
  • Boudjogra M; Hôpital Pitié-Salpêtrière, Service d'Hématologie Biologique, Paris, France;
  • Tzenou T; First Department of Propaedeutic Medicine, University of Athens, Athens, Greece;
  • Chatzouli M; Hematology Department, Nikea General Hospital, Piraeus, Greece;
  • Chu CC; The Feinstein Institute for Medical Research, North Shore-Long Island Jewish Health System, Manhasset, NY;
  • Veronese S; Molecular Pathology Unit and Haematology Department, Niguarda Cancer Center, Niguarda Ca' Granda Hospital, Milan, Italy;
  • Gardiner A; Department of Haematology, Royal Bournemouth Hospital, Bournemouth, United Kingdom;
  • Mansouri L; Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden;
  • Smedby KE; Department of Medicine, Solna, Clinical Epidemiology Unit, Karolinska Institutet, Stockholm, Sweden;
  • Pedersen LB; Department of Hematology, Rigshospitalet, Copenhagen, Denmark;
  • Moreno D; ImMunoGeneTics (IMGT), Université de Montpellier, Laboratoire d'Informatique Gaspard-Monge, Institut de Génétique Humaine, Montpellier, France;
  • Van Lom K; Department of Hematology, Erasmus Medical Center, University Medical Center Rotterdam, Rotterdam, The Netherlands;
  • Giudicelli V; ImMunoGeneTics (IMGT), Université de Montpellier, Laboratoire d'Informatique Gaspard-Monge, Institut de Génétique Humaine, Montpellier, France;
  • Francova HS; Central European Institute of Technology, Masaryk University and University Hospital Brno, Brno, Czech Republic;
  • Nguyen-Khac F; Hematology Department and University Pierre et Marie Curie, Hopital Pitie-Salpetriere, Paris, France;
  • Panagiotidis P; First Department of Propaedeutic Medicine, University of Athens, Athens, Greece;
  • Juliusson G; Lund University and Hospital Department of Hematology, Lund Stem Cell Center, Lund, Sweden;
  • Angelis L; Department of Informatics, Aristotle University of Thessaloniki, Thessaloniki, Greece;
  • Anagnostopoulos A; Hematology Department and Hematopoietic Cell Transplantation Unit, Georgios Papanicolaou Hospital, Thessaloniki, Greece;
  • Lefranc MP; ImMunoGeneTics (IMGT), Université de Montpellier, Laboratoire d'Informatique Gaspard-Monge, Institut de Génétique Humaine, Montpellier, France;
  • Facco M; Department of Medicine, Hematology and Clinical Immunology Branch, Padua University School of Medicine, Italy; Venetian Institute of Molecular Medicine, Padova, Italy;
  • Trentin L; Department of Medicine, Hematology and Clinical Immunology Branch, Padua University School of Medicine, Italy; Venetian Institute of Molecular Medicine, Padova, Italy;
  • Catherwood M; Department of Hemato-Oncology, Belfast City Hospital, Belfast, United Kingdom;
  • Montillo M; Molecular Pathology Unit and Haematology Department, Niguarda Cancer Center, Niguarda Ca' Granda Hospital, Milan, Italy;
  • Geisler CH; Department of Hematology, Rigshospitalet, Copenhagen, Denmark;
  • Langerak AW; Department of Immunology, Erasmus Medical Center, University Medical Center Rotterdam, Rotterdam, The Netherlands;
  • Pospisilova S; Central European Institute of Technology, Masaryk University and University Hospital Brno, Brno, Czech Republic;
  • Chiorazzi N; The Feinstein Institute for Medical Research, North Shore-Long Island Jewish Health System, Manhasset, NY;
  • Oscier D; Department of Haematology, Royal Bournemouth Hospital, Bournemouth, United Kingdom;
  • Jelinek DF; Department of Immunology, Mayo Clinic, Rochester, MN; and.
  • Darzentas N; Central European Institute of Technology, Masaryk University, Brno, Czech Republic.
  • Belessi C; Hematology Department, Nikea General Hospital, Piraeus, Greece;
  • Davi F; Hematology Department and University Pierre et Marie Curie, Hopital Pitie-Salpetriere, Paris, France;
  • Ghia P; Università Vita-Salute San Raffaele, Milan, Italy; Division of Molecular Oncology and Department of Onco-Hematology, Istituto di Ricovero e Cura a Carattere Scientifico, San Raffaele Scientific Institute, Milan, Italy;
  • Rosenquist R; Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden;
  • Stamatopoulos K; Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University, Uppsala, Sweden; Institute of Applied Biosciences, Centre for Research and Technology-Hellas, Thessaloniki, Greece; Hematology Department and Hematopoietic Cell Transplantation Unit, Georgios Papanicol
Blood ; 125(5): 856-9, 2015 Jan 29.
Article em En | MEDLINE | ID: mdl-25634617
ABSTRACT
An unresolved issue in chronic lymphocytic leukemia (CLL) is whether IGHV3-21 gene usage, in general, or the expression of stereotyped B-cell receptor immunoglobulin defining subset #2 (IGHV3-21/IGLV3-21), in particular, determines outcome for IGHV3-21-utilizing cases. We reappraised this issue in 8593 CLL patients of whom 437 (5%) used the IGHV3-21 gene with 254/437 (58%) classified as subset #2. Within subset #2, immunoglobulin heavy variable (IGHV)-mutated cases predominated, whereas non-subset #2/IGHV3-21 was enriched for IGHV-unmutated cases (P = .002). Subset #2 exhibited significantly shorter time-to-first-treatment (TTFT) compared with non-subset #2/IGHV3-21 (22 vs 60 months, P = .001). No such difference was observed between non-subset #2/IGHV3-21 vs the remaining CLL with similar IGHV mutational status. In conclusion, IGHV3-21 CLL should not be axiomatically considered a homogeneous entity with adverse prognosis, given that only subset #2 emerges as uniformly aggressive, contrasting non-subset #2/IGVH3-21 patients whose prognosis depends on IGHV mutational status as the remaining CLL.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Rearranjo Gênico de Cadeia Pesada de Linfócito B / Leucemia Linfocítica Crônica de Células B / Regulação Leucêmica da Expressão Gênica / Cadeias Pesadas de Imunoglobulinas Tipo de estudo: Prognostic_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Blood Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Rearranjo Gênico de Cadeia Pesada de Linfócito B / Leucemia Linfocítica Crônica de Células B / Regulação Leucêmica da Expressão Gênica / Cadeias Pesadas de Imunoglobulinas Tipo de estudo: Prognostic_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Blood Ano de publicação: 2015 Tipo de documento: Article