Evolution of eligibility criteria for non-transplant randomized controlled trials in adults with acute myeloid leukemia.


Journal

Leukemia
ISSN: 1476-5551
Titre abrégé: Leukemia
Pays: England
ID NLM: 8704895

Informations de publication

Date de publication:
08 2022
Historique:
received: 09 05 2022
accepted: 27 05 2022
revised: 25 05 2022
pubmed: 7 6 2022
medline: 4 8 2022
entrez: 6 6 2022
Statut: ppublish

Résumé

Eligibility criteria for clinical trials are intended to select suitable study subjects but can limit trial participation and generalization of results. While reported for other cancers, non-enrollment rates and evolution of eligibility criteria over time have so far not been studied for randomized controlled trials (RCTs) involving adults with acute myeloid leukemia (AML). Among 3698 studies published between 2010 and 2020, including 447 involving prospective clinical trials, we identified 75 phase three RCTs testing non-transplant therapies for adults with AML. Only 31 studies (41%) provided information on non-enrollment; in these studies, the median non-enrollment rate was 23%, primarily attributed to restrictive eligibility criteria. In 95% of trials, eligibility criteria were reported with the total number per trial increasing over time (P < 0.001), particularly in industry-funded trials. A total of 27 eligibility criteria were used across trials, mostly concerning comorbidities or performance status, with eight of them becoming more common over time. The concordance with recent ASCO - Friends of Cancer Research eligibility criteria recommendations greatly varied, from 35% to 99%. Together, our analyses suggest that the ability to generalize results from non-transplant RCTs may be increasingly limited because of high non-enrollment rates and increasingly restrictive eligibility criteria.

Identifiants

pubmed: 35660798
doi: 10.1038/s41375-022-01624-y
pii: 10.1038/s41375-022-01624-y
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2002-2008

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer Nature Limited.

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Auteurs

Corentin Orvain (C)

Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Department of Medicine, Division of Hematology, University of Washington, Seattle, WA, USA.
Maladies du Sang, CHU d'Angers, Angers, France.
Fédération Hospitalo-Universitaire Grand-Ouest Acute Leukemia, FHU-GOAL, Angers, France.
Université d'Angers, Inserm UMR 1307, CNRS UMR 6075, Nantes Université, CRCI2NA, F-49000, Angers, France.

Megan Othus (M)

Public Health Sciences Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.

Gurleen Johal (G)

Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Department of Medicine, Division of Hematology, University of Washington, Seattle, WA, USA.

Mathilde Hunault-Berger (M)

Maladies du Sang, CHU d'Angers, Angers, France.
Fédération Hospitalo-Universitaire Grand-Ouest Acute Leukemia, FHU-GOAL, Angers, France.
Université d'Angers, Inserm UMR 1307, CNRS UMR 6075, Nantes Université, CRCI2NA, F-49000, Angers, France.

Frederick R Appelbaum (FR)

Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Department of Medicine, Division of Medical Oncology, University of Washington, Seattle, WA, USA.

Roland B Walter (RB)

Clinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA, USA. rwalter@fredhutch.org.
Department of Medicine, Division of Hematology, University of Washington, Seattle, WA, USA. rwalter@fredhutch.org.
Department of Laboratory Medicine & Pathology, University of Washington, Seattle, WA, USA. rwalter@fredhutch.org.
Department of Epidemiology, University of Washington, Seattle, WA, USA. rwalter@fredhutch.org.

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