Oral Selinexor–Dexamethasone for Triple-Class Refractory Multiple Myeloma

Ajai Chari(Tisch Hospital), Dan T. Vogl(Tisch Hospital), Maria Gavriatopoulou(National and Kapodistrian University of Athens), Ajay K. Nooka(Emory University), Andrew J. Yee(Massachusetts General Hospital), Carol Ann Huff(Johns Hopkins University), Philippe Moreau(Tisch Hospital), David Dingli(Mayo Clinic in Arizona), Craig E. Cole(University of Michigan), Sagar Lonial(Emory University), Meletios Α. Dimopoulos(National and Kapodistrian University of Athens), A. Keith Stewart(Tisch Hospital), Joshua Richter(Hackensack University Medical Center), Ravi Vij(Washington University in St. Louis), Sascha A. Tuchman(University of North Carolina at Chapel Hill), Marc S. Raab(Heidelberg University), Katja Weisel(Universität Hamburg), Michel Delforge(Tisch Hospital), Robert F. Cornell(Tisch Hospital), David Kaminetzky(NYU Langone Health), James E. Hoffman(University of Miami), Luciano J. Costa(University of Alabama at Birmingham), Terri L. Parker(Yale University), Moshe Levy(Baylor University Medical Center), Martin Schreder(Universitätsklinikum Würzburg), Nathalie Meuleman(Université Libre de Bruxelles), Laurent Frenzel(Hôpital Necker-Enfants Malades), Mohamad Mohty(Sorbonne Université), Sylvain Choquet(Sorbonne Université), Gary J. Schiller(University of California, Los Angeles), Raymond L. Comenzo(Tufts Medical Center), Monika Engelhardt(University of Freiburg), Thomas Illmer(Tisch Hospital), Philip Vlummens(Ghent University Hospital), Chantal Doyen(Tisch Hospital), Thierry Façon(Tisch Hospital), Lionel Karlin(Hôpital Lyon Sud), Aurore Perrot(Centre Hospitalier Régional et Universitaire de Nancy), Klaus Podar(Tisch Hospital), Michael Kauffman(Tisch Hospital), Sharon Shacham(Tisch Hospital), Lingling Li(Tisch Hospital), Shijie Tang(Tisch Hospital), Carla Picklesimer(Tisch Hospital), Jean‐Richard Saint‐Martin(Tisch Hospital), Marsha Crochiere(Tisch Hospital), Hua Chang(Tisch Hospital), Samir Parekh(Tisch Hospital), Yosef Landesman(Tisch Hospital), Jatin J. Shah(Tisch Hospital), Paul G. Richardson(Dana-Farber Cancer Institute), Sundar Jagannath(Tisch Hospital)
New England Journal of Medicine
August 21, 2019
Cited by 669Open Access
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Abstract

BACKGROUND: Selinexor, a selective inhibitor of nuclear export compound that blocks exportin 1 (XPO1) and forces nuclear accumulation and activation of tumor suppressor proteins, inhibits nuclear factor κB, and reduces oncoprotein messenger RNA translation, is a potential novel treatment for myeloma that is refractory to current therapeutic options. METHODS: We administered oral selinexor (80 mg) plus dexamethasone (20 mg) twice weekly to patients with myeloma who had previous exposure to bortezomib, carfilzomib, lenalidomide, pomalidomide, daratumumab, and an alkylating agent and had disease refractory to at least one proteasome inhibitor, one immunomodulatory agent, and daratumumab (triple-class refractory). The primary end point was overall response, defined as a partial response or better, with response assessed by an independent review committee. Clinical benefit, defined as a minimal response or better, was a secondary end point. RESULTS: A total of 122 patients in the United States and Europe were included in the modified intention-to-treat population (primary analysis), and 123 were included in the safety population. The median age was 65 years, and the median number of previous regimens was 7; a total of 53% of the patients had high-risk cytogenetic abnormalities. A partial response or better was observed in 26% of patients (95% confidence interval, 19 to 35), including two stringent complete responses; 39% of patients had a minimal response or better. The median duration of response was 4.4 months, median progression-free survival was 3.7 months, and median overall survival was 8.6 months. Fatigue, nausea, and decreased appetite were common and were typically grade 1 or 2 (grade 3 events were noted in up to 25% of patients, and no grade 4 events were reported). Thrombocytopenia occurred in 73% of the patients (grade 3 in 25% and grade 4 in 33%). Thrombocytopenia led to bleeding events of grade 3 or higher in 6 patients. CONCLUSIONS: Selinexor-dexamethasone resulted in objective treatment responses in patients with myeloma refractory to currently available therapies. (Funded by Karyopharm Therapeutics; STORM ClinicalTrials.gov number, NCT02336815.).


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