https://doi.org/10.55788/24d4d50c
Luspatercept has been shown to improve erythropoiesis and increase platelet and neutrophil counts in patients with LR-MDS [1,2]. Dr Matteo Della Porta (Humanitas Cancer Centre Milan, Italy) presented the results of an interim analysis of the phase 3 COMMANDS trial (NCT03682536), which compared luspatercept with ESAs in ESA-naïve participants with transfusion-dependent LR-MDS [3]. The study randomised 356 participants 1:1 to luspatercept or epoetin alfa for the treatment of anaemia. The primary endpoint was red blood cell transfusion independence for at least 12 weeks during the 24-week treatment period with a concurrent mean haemoglobin increase of at least 1.5 g/dL.
Luspatercept outperformed epoetin alfa for the primary endpoint: 58.5% of the participants in the experimental arm achieved the primary endpoint versus 31.2% in the control arm (P<0.0001). All subgroup analyses favoured treatment with luspatercept over epoetin alfa, except for the subgroup of participants without ring sideroblasts. Dr Della Porta highlighted the results of an exploratory analysis where participants with SF3B1, SF3B1a, ASXL1, and TET2 mutations were likely to benefit significantly more from luspatercept than from epoetin alfa.
The treatment discontinuation rate was 44% in the luspatercept and 60% in the epoetin alfa arm. Lack of efficacy was the main reason for treatment discontinuation in the luspatercept (15.7%) and epoetin alfa arm (32.4%). Finally, treatment-emergent adverse events were balanced between the two arms, including low rates of progression to acute myeloid leukaemia.
- Fenaux P, et al. N Eng J Med. 2020;382:140–151
- Garcia-Manero G, et al. 2022;139(4):624–629
- Della Porta MG, et al. Luspatercept versus epoetin alfa for treatment of anemia in ESA-naïve lower-risk myelodysplastic syndromes patients requiring RBC transfusions: data from the phase 3 COMMANDS study. Plenary abstracts session, EHA 2023 Annual Congress, 8─11 June, Frankfurt, Germany.
Copyright ©2023 Medicom Medical Publishers
Posted on
Previous Article
« REVIVE: Rusfertide meets the primary endpoint in PV Next Article
Letter from the Editor »
« REVIVE: Rusfertide meets the primary endpoint in PV Next Article
Letter from the Editor »
Table of Contents: EHA 2023
Featured articles
Multiple Myeloma
Can we combine teclistamab and nirogacestat for the treatment of RRMM?
Encouraging results for low-dose belantamab mafodotin plus nirogacestat in patients with RRMM
CARTITUDE-4: Cilta-cel meets expectations in lenalidomide-refractory MM
Lymphoma
Radiotherapy or not in patients with PMBCL after immunochemotherapy?
Durable responses for loncastuximab tesirine in relapsed/refractory DLBCL
Zandelisib promising in relapsed/refractory indolent B-cell NHL
Promising data for epcoritamab plus R-CHOP in untreated DLBCL
Non-Malignant Haematology
Investigational agent OMS906 performs well in PNH
Robust platelet responses with cevidoplenib in ITP
Leukaemia
QuANTUM-First: Updated results on quizartinib in AML with FLT3-ITD
Promising data for ziftomenib in relapsed/refractory NPM1-mutated AML
MRD-positive patients with FLT3-ITD AML may benefit from post-transplant gilteritinib
Deep responses with asciminib in CML-CP
QUIWI: First results suggest a clinical benefit of quizartinib in AML
Miscellaneous
COMMANDS trial: A paradigm shift in LR-MDS-associated anaemia
REVIVE: Rusfertide meets the primary endpoint in PV
Mapping healthy HPSC variations to diagnose haematopoietic abnormalities
High risk of death for individuals with C282Y/C282Y hereditary haemochromatosis and diabetes
Related Articles
February 18, 2021
“Strongly consider an SGLT2-inhibitor in most T2DM patients”
February 26, 2020
New guidelines on the prevention of cardiovascular conditions
January 29, 2024
Pemafibrate reduces microvascular complications of PAD and T2D
© 2024 Medicom Medical Publishers. All rights reserved. Terms and Conditions | Privacy Policy
HEAD OFFICE
Laarderhoogtweg 25
1101 EB Amsterdam
The Netherlands
T: +31 85 4012 560
E: publishers@medicom-publishers.com