Survival among patients with relapsed/refractory diffuse large B cell lymphoma treated with single-agent selinexor in the SADAL study.
DLBCL
Exportin-1
SINE compounds
Selinexor
Journal
Journal of hematology & oncology
ISSN: 1756-8722
Titre abrégé: J Hematol Oncol
Pays: England
ID NLM: 101468937
Informations de publication
Date de publication:
16 07 2021
16 07 2021
Historique:
received:
20
04
2021
accepted:
01
07
2021
entrez:
17
7
2021
pubmed:
18
7
2021
medline:
3
11
2021
Statut:
epublish
Résumé
Patients with RR DLBCL who have received ≥ 2 lines of therapy have limited treatment options and an expected overall survival (OS) of < 6 months. The SADAL study evaluated single-agent oral selinexor in patients with RR DLBCL and demonstrated an overall response rate (ORR) of 29.1% with median duration of response (DOR) of 9.3 months. The analyses described here evaluated a number of subpopulations in order to understand how response correlates with survival outcomes in order to identify patients who could most optimally benefit from selinexor treatment. Median age was 67 years; 44.8% of patients were ≥ 70 years of age. The median OS was 9.0 months (95% CI 6.2, 13.7) at a median follow-up of 14.8 months. The median OS was not reached in patients with a CR or PR, while patients who did not respond have a median OS of 4.9 months (p < 0.0001). Patients < 70 years had an OS of 11.1 months compared with 7.8 months in patients ≥ 70 years. Among patients with or without prior ASCT, the median OS was 10.9 and 7.8 months, respectively. Among patients with disease refractory to the most recent DLBCL treatment regimen, the median OS was 7.0 months compared with 11.1 months for disease not refractory to the most recent treatment. In a patient population in which survival is expected to be < 6 months, treatment with single-agent oral selinexor was associated with a median survival of 9 months. Increased median OS observed in patients responding to selinexor was consistent across subgroups regardless of age, prior ASCT therapy, or refractory status. Randomized studies of selinexor in combination with a variety of other anti-DLBCL agents are planned. This trial was registered at ClinicalTrials.gov (NCT02227251) on August 28, 2014. https://clinicaltrials.gov/ct2/show/NCT02227251 .
Identifiants
pubmed: 34271963
doi: 10.1186/s13045-021-01122-1
pii: 10.1186/s13045-021-01122-1
pmc: PMC8283921
doi:
Substances chimiques
Hydrazines
0
Triazoles
0
selinexor
31TZ62FO8F
Banques de données
ClinicalTrials.gov
['NCT02227251']
Types de publication
Clinical Trial
Letter
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
111Informations de copyright
© 2021. The Author(s).
Références
Blood. 2012 Nov 29;120(23):4621-34
pubmed: 23034282
Leuk Lymphoma. 2021 Apr;62(4):828-836
pubmed: 33274677
Acta Oncol. 2015 Jun;54(6):916-23
pubmed: 25519707
Clin Cancer Res. 2021 Jun 15;27(12):3307-3316
pubmed: 33785483
Semin Cancer Biol. 2014 Aug;27:74-86
pubmed: 24755012
Cancer Commun (Lond). 2021 Mar;41(3):229-239
pubmed: 33482051
Am J Hematol. 2013 Oct;88(10):890-4
pubmed: 23813874
Hematol Oncol. 2021 Feb 13;:
pubmed: 33583077
Ann Oncol. 2015 Jun;26(6):1058-1068
pubmed: 25635006
Lancet Oncol. 2020 Jul;21(7):978-988
pubmed: 32511983
Lancet Haematol. 2020 Jul;7(7):e511-e522
pubmed: 32589977