In this episode (12.15), Medicom’s correspondent covers 6 presentations from the annual meeting of the European Hematology Association (EHA 2023), held from 8-11 June, in Frankfurt, Germany.
The topics discussed are:
- COMMANDS trial: Paradigm shift in LR-MDS-associated anaemia
Luspatercept was superior to epoetin alfa in treating anaemia in erythropoiesis-stimulating agent (ESA)-naïve patients with transfusion-dependent lower-risk myelodysplastic syndromes. The safety profile of luspatercept was manageable and predictable. - CARTITUDE-4: cilta-cel meets expectations in lenalidomide-refractory MM
Cilta-cel was superior to standard-of-care in patients with lenalidomide-refractory multiple myeloma (MM), results from the phase 3 CARTITUDE-4 trial showed. According to the authors, cilta-cel has the potential to become the new standard-of-care for patients with lenalidomide-refractory MM after a first relapse - Good results for zandelisib in relapsed/refractory indolent B-cell NHL
Zandelisib displayed a high response rate in heavily pre-treated patients with relapsed/refractory indolent B-cell non-Hodgkin’s lymphoma, including patients with poor prognoses. The safety analysis revealed a low rate of grade ≥ 3 adverse events of special interest. - Promising data for zitomenib in relapsed/refractory NPM1-mutated AML
Ziftomenib displayed encouraging clinical activity in a heavily pre-treated population of patients with relapsed/refractory NPM1-mutated acute myeloid leukaemia. The agent was well-tolerated and the lack of predicted adverse drug-drug interactions suggests that ziftomenib could be explored in combination with other agents. - REVIVE: rusfertide meets primary endpoint in PV
Compared to placebo, rusfertide was associated with improved response rates in patients with polycythaemia vera (PV). The drug met all the efficacy endpoints, was well-tolerated, and is currently being investigated in the phase 3 VERIFY trial. - Investigational agent performs well in PNH
The MASP-3 inhibitor OMS906 appeared safe and displayed encouraging signs of efficacy in the interim analysis of a phase 1b trial involving patients with treatment-naïve paroxysmal nocturnal haemoglobinuria (PNH). Several trials are underway to further evaluate this agent in the PNH population.
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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
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