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Long-term outcome of imatinib 400 mg compared to imatinib 600 mg or imatinib 400 mg daily in combination with cytarabine or pegylated interferon alpha 2a for chronic myeloid leukaemia: results from the French SPIRIT phase III randomised trial.

Authors :
Guilhot F
Rigal-Huguet F
Guilhot J
Guerci-Bresler AP
Maloisel F
Rea D
Coiteux V
Gardembas M
Berthou C
Vekhoff A
Jourdan E
Berger M
Fouillard L
Alexis M
Legros L
Rousselot P
Delmer A
Lenain P
Escoffre Barbe M
Gyan E
Bulabois CE
Dubruille V
Joly B
Pollet B
Cony-Makhoul P
Johnson-Ansah H
Mercier M
Caillot D
Charbonnier A
Kiladjian JJ
Chapiro J
Penot A
Dorvaux V
Vaida I
Santagostino A
Roy L
Zerazhi H
Deconinck E
Maisonneuve H
Plantier I
Lebon D
Arkam Y
Cambier N
Ghomari K
Miclea JM
Glaisner S
Cayuela JM
Chomel JC
Muller M
Lhermitte L
Delord M
Preudhomme C
Etienne G
Mahon FX
Nicolini FE
Source :
Leukemia [Leukemia] 2021 Aug; Vol. 35 (8), pp. 2332-2345. Date of Electronic Publication: 2021 Jan 22.
Publication Year :
2021

Abstract

The STI571 prospective randomised trial (SPIRIT) French trial is a four-arm study comparing imatinib (IM) 400 mg versus IM 600 mg, IM 400 mg + cytarabine (AraC), and IM 400 mg + pegylated interferon alpha2a (PegIFN-α2a) for the front-line treatment of chronic-phase chronic myeloid leukaemia (CML). Long-term analyses included overall and progression-free survival, molecular responses to treatment, and severe adverse events. Starting in 2003, the trial included 787 evaluable patients. The median overall follow-up of the patients was 13.5 years (range 3 months to 16.7 years). Based on intention-to-treat analyses, at 15 years, overall and progression-free survival were similar across arms: 85%, 83%, 80%, and 82% and 84%, 87%, 79%, and 79% for the IM 400 mg (N = 223), IM 600 mg (N = 171), IM 400 mg + AraC (N = 172), and IM 400 mg + PegIFN-α2a (N = 221) arms, respectively. The rate of major molecular response at 12 months and deep molecular response (MR4) over time were significantly higher with the combination IM 400 mg + PegIFN-α2a than with IM 400 mg: p = 0.0001 and p = 0.0035, respectively. Progression to advanced phases and secondary malignancies were the most frequent causes of death. Toxicity was the main reason for stopping AraC or PegIFN-α2a treatment.<br /> (© 2021. The Author(s), under exclusive licence to Springer Nature Limited part of Springer Nature.)

Details

Language :
English
ISSN :
1476-5551
Volume :
35
Issue :
8
Database :
MEDLINE
Journal :
Leukemia
Publication Type :
Academic Journal
Accession number :
33483613
Full Text :
https://doi.org/10.1038/s41375-020-01117-w