Scientific article
English

Addition of the nuclear export inhibitor selinexor to standard intensive treatment for elderly patients with acute myeloid leukemia and high risk myelodysplastic syndrome

Published inLeukemia, vol. 36, no. 9, p. 2189-2195
Publication date2022-09
First online date2022-07-22
Abstract

Treatment results of AML in elderly patients are unsatisfactory. In an open label randomized phase II study, we investigated whether addition of the XPO1 inhibitor selinexor to intensive chemotherapy would improve outcome in this population. 102 AML patients > 65 years of age (median 69 (65-80)) were randomly assigned to standard chemotherapy (3 + 7) with or without oral selinexor 60 mg twice weekly (both arms n = 51), days 1-24. In the second cycle, cytarabine 1000 mg/m2twice daily, days 1-6 with or without selinexor was given. CR/CRi rates were significantly higher in the control arm than in the investigational arm (80% (95% C.I. 69-91%) vs. 59% (45-72%; p = 0.018), respectively). At 18 months, event-free survival was 45% for the control arm versus 26% for the investigational arm (Cox-p = 0.012) and overall survival 58% vs. 33%, respectively (p = 0.009). AML and infectious complications accounted for an increased death rate in the investigational arm. Irrespective of treatment, MRD status after two cycles appeared to be correlated with survival. We conclude that the addition of selinexor to standard chemotherapy does negatively affect the therapeutic outcome of elderly AML patients. (Netherlands Trial Registry number NL5748 (NTR5902), www.trialregister.nl ).

Keywords
  • Active Transport, Cell Nucleus
  • Aged
  • Antineoplastic Combined Chemotherapy Protocols
  • Cytarabine
  • Humans
  • Hydrazines
  • Leukemia, Myeloid, Acute
  • Myelodysplastic Syndromes
  • Triazoles
Citation (ISO format)
JANSSEN, J J W M et al. Addition of the nuclear export inhibitor selinexor to standard intensive treatment for elderly patients with acute myeloid leukemia and high risk myelodysplastic syndrome. In: Leukemia, 2022, vol. 36, n° 9, p. 2189–2195. doi: 10.1038/s41375-022-01657-3
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Article (Published version)
accessLevelRestricted
Identifiers
Additional URL for this publicationhttps://www.nature.com/articles/s41375-022-01657-3
Journal ISSN0887-6924
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9downloads

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