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The added value of multi-state modelling in a randomized controlled trial: The HOVON 102 study re-analyzed.

Authors :
Bakunina K
Putter H
Versluis J
Koster EAS
van der Holt B
Manz MG
Breems DA
Gjertsen BT
Cloos J
Valk PJM
Passweg J
Pabst T
Ossenkoppele GJ
Löwenberg B
Cornelissen JJ
de Wreede LC
Source :
Cancer medicine [Cancer Med] 2022 Feb; Vol. 11 (3), pp. 630-640. Date of Electronic Publication: 2021 Dec 24.
Publication Year :
2022

Abstract

Clofarabine is an active antileukemic drug for subgroups of patients with acute myeloid leukemia (AML). Multi-state models can provide additional insights to supplement the original intention-to-treat analysis of randomized controlled trials (RCT). We re-analyzed the HOVON102/SAKK30/09 phase III RCT for newly diagnosed AML patients, which randomized between standard induction chemotherapy with or without clofarabine. Using multi-state models, we evaluated the effects of induction chemotherapy outcomes (complete remission [CR], measurable residual disease [MRD]), and post-remission therapy with allogeneic stem cell transplantation [alloSCT] on relapse and death. Through the latter a consistent reduction in the hazard of relapse in the clofarabine arm compared to the standard arm was found, which occurred irrespective of MRD status or post-remission treatment with alloSCT, demonstrating a strong and persistent antileukemic effect of clofarabine. During the time period between achieving CR and possible post-remission treatment with alloSCT, non-relapse mortality was higher in patients receiving clofarabine. An overall net benefit of treatment with clofarabine was identified using the composite endpoint current leukemia-free survival (CLFS). In conclusion, these results enforce and extend the earlier reported beneficial effect of clofarabine in AML and show that multi-state models further detail the effect of treatment on competing and series of events.<br /> (© 2021 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
2045-7634
Volume :
11
Issue :
3
Database :
MEDLINE
Journal :
Cancer medicine
Publication Type :
Academic Journal
Accession number :
34953042
Full Text :
https://doi.org/10.1002/cam4.4392