High-grade B-cell lymphoma with MYC and BCL2 and/or BCL6 rearrangements with diffuse large B-cell lymphoma morphology

Author:

Scott David W.123,King Rebecca L.43,Staiger Annette M.563,Ben-Neriah Susana13,Jiang Aixiang73,Horn Heike63,Mottok Anja183,Farinha Pedro13,Slack Graham W.13,Ennishi Daisuke13,Schmitz Norbert93,Pfreundschuh Michael93,Nowakowski Grzegorz S.103,Kahl Brad S.113,Connors Joseph M.123,Gascoyne Randy D.13,Ott German53,Macon William R.43,Rosenwald Andreas83

Affiliation:

1. Centre for Lymphoid Cancer, British Columbia Cancer Agency, Vancouver, Canada;

2. Department of Medicine, University of British Columbia, Vancouver, Canada;

3. Washington University School of Medicine, St. Louis, MO

4. Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN;

5. Department of Clinical Pathology, Robert-Bosch-Krankenhaus, Stuttgart, Germany;

6. Dr. Margarete Fischer-Bosch Institute of Clinical Pharmacology, Stuttgart and University of Tuebingen, Tuebingen, Germany;

7. Department of Molecular Biology and Biochemistry, Simon Fraser University, Vancouver, Canada;

8. Institute of Pathology, Würzburg University and Comprehensive Cancer Center Mainfranken, Würzburg, Germany;

9. Department of Medicine, Hematology and Oncology, University Hospital Muenster, Muenster, Germany;

10. Department of Internal Medicine I, Saarland University Medical School, Homburg/Saar, Germany;

11. Department of Oncology, Mayo Clinic, Rochester, MN; and

Abstract

Key Points HGBL-DH/TH makes up 8% of de novo DLBCL, with HGBL-DH/TH with BCL2 rearrangement being a GCB phenomenon. Restricting FISH testing to tumors with dual protein expression and GCB subtype results in testing <15% of tumors, but missing ∼35% of HGBL-DH/TH.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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