Safety and efficacy of selinexor in relapsed or refractory multiple myeloma and Waldenstrom macroglobulinemia

Author:

Chen Christine12,Siegel David3,Gutierrez Martin3,Jacoby Meagan4,Hofmeister Craig C.5ORCID,Gabrail Nashat6,Baz Rachid7ORCID,Mau-Sorensen Morten8,Berdeja Jesus G.9,Savona Michael10ORCID,Savoie Lynn11,Trudel Suzanne12,Areethamsirikul Nuchanan12,Unger T. J.12,Rashal Tami12,Hanke Tim12,Kauffman Michael12,Shacham Sharon12,Reece Donna12

Affiliation:

1. Division of Medical Oncology & Hematology, Princess Margaret Cancer Centre, Toronto, ON, Canada;

2. The University of Toronto, Toronto, ON, Canada;

3. Department of Hematology, John Theurer Cancer Center, Hackensack, NJ;

4. Siteman Cancer Center, Washington University in Saint Louis, Saint Louis, MO;

5. Department of Internal Medicine, Division of Hematology, The Ohio State University, Columbus, OH;

6. Gabrail Cancer Institute, Canton, OH;

7. Department of Malignant Hematology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL;

8. Department of Oncology, Rigshospitalet, Copenhagen, Denmark;

9. Blood Cancer Research Program, Sarah Cannon Research Institute, Nashville, TN;

10. Division of Hematology & Oncology, Vanderbilt-Ingram Cancer Center/Vanderbilt University Medical Center, Nashville, TN;

11. Tom Baker Cancer Centre Division of Hematology, University of Calgary, Calgary, AB, Canada; and

12. Karyopharm Therapeutics Inc, Newton, MA

Abstract

Key Points Selinexor is an oral XPO1 inhibitor with antimyeloma activity. The RP2D is 45 mg/m2 (80 mg) selinexor plus 20 mg dexamethasone given twice weekly.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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