It is with great pleasure to introduce this peer-reviewed ASH 2022 Medicom Conference Report. It again was organized as a hybrid meeting, a format that currently is available for most medical conferences.
The ASH annual meeting, now held in New Orleans, is a great event to which everyone is looking forward. It offers the opportunity to get informed in benign as well as malignant haematology. Basic, translational, and clinical topics were covered in a wonderful programme. From this years’ ASH meeting we selected a number of interesting abstracts that will most likely change your daily practice now or in the near future. The abstracts are summarised in a way that the information is easy to digest in a rather short time.
The rapidly evolving field of immunotherapy, including bispecific antibody and CAR T-cell treatment applied in a variety of haematological malignancies, got a lot of attention. Gene therapy is emerging, resulting in new treatments for haemoglobinopathies and haemophilia. The further deciphering of the molecular basis of benign and malignant disease by al kind of new technologies is striking.
Treatment of acute myeloid leukemia, a disease in which no new developments emerged for a long time, is rapidly changing with the development of new effective targeted treatments and successful maintenance treatment. Especially in the patients unfit for intensive chemotherapy, new avenues are opened. But also in the other malignant and non-malignant haematological diseases, new drugs are rapidly developed and approved by the regulatory authorities. Measurable residual disease becomes an important surrogate endpoint for outcome in many heamatological malignancies and helps to inform treatment.
You will find snapshots of all these new developments in this report. I can imagine that these are helpful in your daily practice and I am certain that you will enjoy.
Gert Ossenkoppele
Biography
Gert Ossenkoppele was appointed in 2003 as professor of Hematology at the VU University Medical Center in Amsterdam. He obtained his doctorate of medicine at that same University in 1977. He is board certified in Hematology and Internal medicine (1984). The title of his PhD thesis (1990) was: ”Differentiation induction in AML”. Gert Ossenkoppele has authored over 450 publications in peer-reviewed journals and is invited speaker at many national and international scientific meetings. His research interests is mainly translational and include the (stem cell) biology of AML, leukemic stem cell target discovery, immunotherapy and measurable residual disease (MRD) detection using flow cytometry to inform treatment of AML. He is PI of national and international clinical trials in myeloid malignancies. He is reviewer on a regular basis for many high impact hematological journals (Blood, Leukemia, Haematologica, JAMA Oncology, Lancet Oncology NEJM). He chairs the AML working party of HOVON (Dutch-Belgian Hematology Trial Group) and recently stepped down as vice-chair of the HOVON Executive Board. He is a lead participant of the AML Work package of the European LeukemiaNet(ELN) as well as a board member of the ELN foundation. He co-leads the AML WP of HARMONY. He rotated of as board member of the European Hematology Association and was very recently appointed as vice-chair of the EHA Educational Committee. He just rotated off as chair of the AML Scientific working group of EHA and is now a member of this group. He is member of the Global and EU steering committee of the AMLGlobalPortal an educational portal for hematologists (www.amlglobalportal.com). He chairs the institutional DSMB of his University. He has now because of retirement an honorary position as hematologist at the Amsterdam University Medical Center.
Conflicts of Interest
Prof. Gert Ossenkoppele received research support from Novartis, J&J and BMS-Celgene. He functions as a consultant for J&J, Daiichi-Sanyko, BMS-Celgene, Servier, and Roche. Lastly, he is a member of the advisory boards of Novartis, Pfizer, Abbvie, J&J, Daiichi-Sanyko, BMS-Celgene, AGIOS, Amgen, Astellas, Roche, Jazz pharmaceuticals, and Merus.
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Table of Contents: ASH 2022
Featured articles
Acute Lymphoblastic Leukaemia
Blinatumomab candidate for standard-of-care in newly diagnosed B-ALL
High-dose methotrexate or standard interim maintenance in young patients with ALL?
Acute Myeloid Leukaemia
Excellent results for triplet regimen in FLT3-mutated AML
MRD by qPCR prognostic of outcomes in venetoclax-treated NPM1-mutated AML
Promising results for triplet therapy with magrolimab in AML
Should we use intensive chemotherapy prior to allo-HCT in relapsed/refractory AML?
Chronic Leukaemia
Zanubrutinib wins battle of BTK inhibitors in relapsed or refractory CLL/SLL
Ibrutinib plus venetoclax displays long-term benefits in CLL
Multiple Myeloma
Talquetamab further investigated in heavily pre-treated MM after promising phase 2 data
Promising results of elranatamab for MM in phase 2 MagnetisMM-3 trial
Deep and durable responses for quadruple therapy in smouldering MM
Ultra-sensitive MRD assessment in MM with BloodFlow
CAR-Hematotox score proves useful in relapsed/refractory MM
Head-to-head: VMP versus Rd in transplant-ineligible MM
Lymphoma
Ibrutinib added to ASCT improves clinical outcomes in mantle cell lymphoma
High-dose chemotherapy plus ASCT superior to standard immuno-chemotherapy in primary CNS lymphoma
Odronextamab has considerable anti-tumour effects in relapsed/refractory diffuse large B-cell lymphoma and follicular lymphoma
Excellent results for AFM13-complexed NK cells in CD30-positive lymphoma
CAR-Hematotox score predicts toxicity, infections, and clinical outcomes in MCL
Myeloproliferative Neoplasms
Efgartigimod successful in immune thrombocytopenia
INCA033989: novel investigational agent for CALR-mutated MPN
Ruxolitinib mediates clonal evolution of RAS pathway mutations in MPN
Immune Thrombocytopenia
Long-term risk for haematologic disease in persistent, isolated mild thrombocytopenia
Various Topics
C1 inhibitor deficiency linked to thrombosis
Durable responses to gene therapy in haemophilia A
Long-term benefits from beti-cel in transfusion-dependent β-thalassaemia
Neutrodiet: non-restricted diet is the preferred option after SCT
Iptacopan offers solution for patients with PNH and residual anaemia after standard-of-care
Novel therapy may replace standard-of-care prophylaxis for GVHD
LMWH does not result in higher live birth rates in women with inherited thrombophilia
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