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Outcome prediction by interim positron emission tomography and IgM monoclonal gammopathy in diffuse large B-cell lymphoma.
Johansson, Patricia; Alig, Stefan; Richter, Julia; Hanoun, Christine; Rekowski, Jan; Dürig, Jan; Ylstra, Bauke; de Jong, Daphne; Klapper, Wolfram; Alizadeh, Ash A; Dührsen, Ulrich; Hüttmann, Andreas.
Affiliation
  • Johansson P; Department of Hematology, West German Cancer Center, University Hospital Essen, University of Duisburg-Essen, Hufelandstraße 55, 45147, Essen, Germany.
  • Alig S; Institute of Cell Biology (Cancer Research), Faculty of Medicine, University of Duisburg-Essen, Essen, Germany.
  • Richter J; Department of Medicine, Divisions of Oncology and Hematology, Stanford University, Stanford, CA, USA.
  • Hanoun C; Department of Hematopathology, University Hospital Schleswig-Holstein, Kiel, Germany.
  • Rekowski J; Department of Hematology, West German Cancer Center, University Hospital Essen, University of Duisburg-Essen, Hufelandstraße 55, 45147, Essen, Germany.
  • Dürig J; Institute for Medical Informatics, Biometry and Epidemiology, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
  • Ylstra B; Department of Hematology, West German Cancer Center, University Hospital Essen, University of Duisburg-Essen, Hufelandstraße 55, 45147, Essen, Germany.
  • de Jong D; Department of Pathology, Cancer Center Amsterdam, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
  • Klapper W; Department of Pathology, Cancer Center Amsterdam, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
  • Alizadeh AA; Department of Hematopathology, University Hospital Schleswig-Holstein, Kiel, Germany.
  • Dührsen U; Department of Medicine, Divisions of Oncology and Hematology, Stanford University, Stanford, CA, USA.
  • Hüttmann A; Stanford Cancer Institute, Institute for Stem Cell Biology & Regenerative Medicine, Stanford, CA, USA.
Ann Hematol ; 102(12): 3445-3455, 2023 Dec.
Article de En | MEDLINE | ID: mdl-37566280
In diffuse large B-cell lymphoma (DLBCL), a positive interim positron emission tomography (PET) scan predicts treatment failure, but the proportion of high-risk patients thus identified is small. To improve prediction, we combined the interim PET result with the presence or absence of an associated IgM gammopathy. Of 108 DLBCL patients participating in a prospective trial, nine (8%) were interim PET positive and 19 (18%) had an IgM gammopathy. The monoclonal protein was not associated with distinguishing genetic features, and its light chain restriction was not always concordant with the light chain restriction of the lymphoma. The information provided by interim PET and IgM gammopathy was combined to dichotomize the population into sizeable high-risk (1-2 adverse factors) and low-risk groups (no adverse factor) with widely different outcomes (population size, 25% vs. 75%; 3-year risk of progression, 51% vs. 10%; 3-year overall survival, 64% vs. 95%). Multivariable analyses including established risk factors revealed the interim PET result and the IgM gammopathy status to be the only factors significantly associated with outcome. Information about interim PET response and IgM gammopathy may be useful in studies testing risk-adapted treatment strategies.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Paraprotéinémies / Lymphome B diffus à grandes cellules Type d'étude: Prognostic_studies / Risk_factors_studies Limites: Humans Langue: En Journal: Ann Hematol Sujet du journal: HEMATOLOGIA Année: 2023 Type de document: Article Pays d'affiliation: Allemagne Pays de publication: Allemagne

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Paraprotéinémies / Lymphome B diffus à grandes cellules Type d'étude: Prognostic_studies / Risk_factors_studies Limites: Humans Langue: En Journal: Ann Hematol Sujet du journal: HEMATOLOGIA Année: 2023 Type de document: Article Pays d'affiliation: Allemagne Pays de publication: Allemagne