Targetable genetic features of primary testicular and primary central nervous system lymphomas

Author:

Chapuy Bjoern1,Roemer Margaretha G. M.12,Stewart Chip3,Tan Yuxiang4,Abo Ryan P.5,Zhang Liye4,Dunford Andrew J.3,Meredith David M.6,Thorner Aaron R.5,Jordanova Ekaterina S.7,Liu Gang4,Feuerhake Friedrich8,Ducar Matthew D.5,Illerhaus Gerald9,Gusenleitner Daniel4,Linden Erica A.10,Sun Heather H.6,Homer Heather1,Aono Miyuki1,Pinkus Geraldine S.6,Ligon Azra H.6,Ligon Keith L.6,Ferry Judith A.11,Freeman Gordon J.1,van Hummelen Paul5,Golub Todd R.312,Getz Gad311,Rodig Scott J.6,de Jong Daphne2,Monti Stefano4,Shipp Margaret A.1

Affiliation:

1. Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA;

2. Department of Pathology, VU University Medical Center, Amsterdam, The Netherlands;

3. Broad Institute, Cambridge, MA;

4. Section of Computational Biomedicine, Boston University School of Medicine, Boston, MA;

5. Center for Cancer Genome Discovery, Dana-Farber Cancer Institute, Boston, MA;

6. Department of Pathology, Brigham and Women’s Hospital, Boston, MA;

7. Center of Gynaecologic Oncology, VU University Medical Center, Amsterdam, The Netherlands;

8. Department of Pathology, Hannover Medical School, Hannover, Germany;

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

10. Massachusetts General Hospital/North Shore Cancer Center, Danvers, MA;

11. Department of Pathology, Massachusetts General Hospital, Boston, MA; and

12. Department of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA

Abstract

Key Points PCNSLs and PTLs have a defining genetic signature that differs from other LBCLs and suggests rational targeted therapies. PCNSLs and PTLs frequently exhibit 9p24.1/PD-L1/PD-L2 copy number alterations and translocations, likely genetic bases of immune evasion.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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