Clinicogenetic risk models predict early progression of follicular lymphoma after first-line immunochemotherapy

Author:

Jurinovic Vindi12,Kridel Robert3,Staiger Annette M.45,Szczepanowski Monika6,Horn Heike45,Dreyling Martin H.1,Rosenwald Andreas7,Ott German4,Klapper Wolfram6,Zelenetz Andrew D.8,Barr Paul M.9,Friedberg Jonathan W.9,Ansell Stephen10,Sehn Laurie H.3,Connors Joseph M.3,Gascoyne Randy D.3,Hiddemann Wolfgang111,Unterhalt Michael1,Weinstock David M.12,Weigert Oliver111

Affiliation:

1. Medical Department III, University Hospital of the Ludwig Maximilians University Munich, Munich, Germany;

2. Institute for Medical Informatics, Biometry and Epidemiology, Ludwig Maximilians University Munich, Munich, Germany;

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

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

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

6. Hematopathology Section, University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany;

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

8. Department of Medicine, Memorial Sloan Kettering Cancer Center, and Weill Medical College of Cornell University, New York, NY;

9. Wilmot Cancer Institute, University of Rochester, Rochester NY;

10. Division of Hematology, Mayo Clinic, Rochester, MN;

11. German Cancer Consortium and German Cancer Research Center, Heidelberg, Germany; and

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

Abstract

Key Points The posttreatment end point progression of FL within 24 months (POD24) is strongly associated with OS. A pretreatment clinicogenetic risk model (m7-FLIPI) predicts POD24 and OS and identifies the smallest subgroup with highest unmet need.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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