CONGRESS HIGHLIGHTS

Highlights in thrombosis and Haemostasis

BJH - volume 13, issue 1, february 2022

C. Hermans MD, PhD

SUMMARY

New therapeutic developments in the field of haemophilia were highlighted at the ASH 2021 congress. These included the results of inhibition of antithrombin production via fitusiran for the prevention of bleeding events in haemophilia A and B patients with or without inhibitors, the success of emicizumab, a bispecific antibody that mimics the action of FVIII, in patients with moderate or mild haemophilia A, and finally the promising results of FVIII fused to the Fc fragment of the immunoglobulins as an agent for FVIII tolerance induction in patients with inhibitors. In the field of antithrombotics, a meta-analysis confirms the place of direct oral anticoagulants in cancer patients with thrombosis. Xarelto has demonstrated its value in patients with visceral venous thrombosis and a large study does not support the thrombogenicity of mRNA-based COVID vaccines.

(BELG J HEMATOL 2022;13(1):37-42)

Read more

Highlights in aggressive and indolent Lymphoma

BJH - volume 13, issue 1, february 2022

J. Blokken PhD, PharmD, T. Feys MBA, MSc

SUMMARY

During the 63rd annual meeting of ASH, again hundreds of interesting oral abstracts and poster presentations in the field of aggressive and indolent lymphoma were discussed. In this article, we will highlight some of the most promising data in the field of diffuse large B-cell lymphoma, classic Hodgkin lymphoma, enteropathy-associated T-cell lymphoma, mantle cell lymphoma and follicular lymphoma.

(BELG J HEMATOL 2022;13(1):29-36)

Read more

Highlights in myelodysplastic Syndromes

BJH - volume 13, issue 1, february 2022

B. Heyrman MD

SUMMARY

The first hybrid ASH meeting lived up to the expectation of bringing new data forward that will change the life of MDS patients. Implementation of NGS in daily practice has unveiled intimate information of the disease and is moving forward into risk scores. A new and better standard risk score will change our treatment approach thereby changing the outcome of our patients. For now, we are watching new molecules grow through different trial phases and becoming impatient to install them into daily practice in the near future. A summary of the most appealing data in the field of MDS is presented here.

(BELG J HEMATOL 2022;13(1):25-8)

Read more

Highlights in chronic myeloid leukaemia and myeloproliferative neoplasm

BJH - volume 13, issue 1, february 2022

D. Mazure MD

SUMMARY

As every year, ASH 2021 brought us updates on current practice, new insights and promising future treatments. I have tried to select the most relevant data from the educational sessions and oral and poster abstracts that can influence our current and near-future practice in chronic myeloid leukaemia (CML) and myeloproliferative neoplasm (MPN).

(BELG J HEMATOL 2022;13(1):17–24)

Read more

Highlights in chronic lymphocytic Leukaemia

BJH - volume 13, issue 1, february 2022

T. Feys MBA, MSc

SUMMARY

The research landscape in chronic lymphocytic leukaemia (CLL) anno 2022 puts a strong focus on the optimal treatment choice in the frontline setting. In this setting, targeted therapy options have largely replaced chemoimmunotherapy as standard of care. However, with this evolution comes a new question: which patient is best treated with a continuous treatment option and who benefits most from a time-limited treatment approach? During ASH 2021, results of several studies looking at both treatment strategies have been presented, further fuelling this debate. Despite the impressive improvements in the frontline setting, a large proportion of patients will eventually relapse or develop refractoriness to the available therapies. To address this medical need, researchers continue to develop new treatment modalities. In this light, ASH 2021 featured promising results with the novel BTK-inhibitor pirtobrutinib and provided a reassuring update of the ASCEN trial evaluating acalabrutinib in the relapsed/refractory setting.

(BELG J HEMATOL 2022;13(1):11–6)

Read more