A randomised evaluation of low‐dose cytosine arabinoside plus lenalidomide versus single‐agent low‐dose cytosine arabinoside in older patients with acute myeloid leukaemia: Results from the LI‐1 trial

Author:

Copland Mhairi1ORCID,Ariti Cono23,Thomas Ian F.2,Upton Laura2,Sydenham Mia2,Mehta Priyanka4ORCID,Islam Shahid5,Kjeldsen Lars6,Burnett Alan K.1,Hills Robert K.7ORCID,Russell Nigel8ORCID,Dennis Mike9ORCID,

Affiliation:

1. Paul O'Gorman Leukaemia Research Centre, School of Cancer Sciences University of Glasgow Glasgow UK

2. Centre for Trials Research Cardiff University Cardiff UK

3. Oxon Epidemiology Madrid Spain

4. University Hospitals of Bristol and Weston NHS Trust Bristol UK

5. Department of Haematology Waikato Hospital Hamilton New Zealand

6. Rigshospitalet Copenhagen University Hospital Copenhagen Denmark

7. Nuffield Department of Population Health University of Oxford Oxford UK

8. Guy's and St Thomas' NHS Trust London UK

9. The Christie Manchester UK

Abstract

SummaryImproving outcomes for older patients with acute myeloid leukaemia remains an unmet need. As part of the LI‐1 trial, we evaluated lenalidomide (LEN) in combination with low‐dose cytosine arabinoside (LDAC) in patients aged >60 years unfit for intensive therapy and compared this to LDAC alone. Two hundred and two patients, randomised 1:1, were evaluable. Overall response rate (CR + CRi) was higher for LDAC + LEN versus LDAC (26% and 13.7% respectively p = 0.031). However, there was no difference in overall survival between the arms (14% and 11.5% at 2 years for LDAC + LEN and LDAC respectively). The addition of LEN was associated with increased toxicity and supportive care requirements.

Funder

Blood Cancer UK

Celgene

Publisher

Wiley

Subject

Hematology

Reference14 articles.

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