Many patients with haematologic malignancies have underlying immune dysfunction and many are treated with chemo- and immunotherapies that are themselves profoundly immunosuppressive. In addition, patients with haematologic malignancies are often older and may have comorbidities, including hypertension and diabetes. Thus, they may be especially susceptible to complications of COVID-19, including hypercoagulability and thrombosis [1].
Prof. William A. Wood (University of North Carolina, USA) presented findings from the ASH Research Collaborative COVID-19 Registry for Hematology (www.ashrc.org), which were simultaneously published in Blood Advances [1,2]. This collaborative research hub was developed to study features and outcomes of COVID-19 in patients with underlying haematologic disorders, including haematologic malignancies. Prof. Wood presented data from 656 patients with haematologic malignancy from 74 sites worldwide who had been entered into the Registry. The most common malignancies were acute leukaemia (33%), non-Hodgkin lymphoma (27%), and myeloma or amyloidosis (16%). Most frequently observed symptoms included fever (73%), cough (67%), dyspnoea (50%), and fatigue (40%). COVID-19-directed therapies, such as hydroxychloroquine or azithromycin, were commonly used.
Overall mortality was 28%. Patients with an estimated prognosis of <12 months from the underlying haematologic malignancy at the time of COVID-19 diagnosis and those with relapsed or refractory disease were at higher risk of moderate-to-severe COVID-19 disease and death. In some cases, patients died after the decision not to be admitted to ICU in favour of a palliative approach.
This data supports the emerging consensus that patients with haematologic malignancies experience significant morbidity and mortality from COVID-19. However, based on their own data, Prof. Wood and colleagues see no reason to withhold intensive therapies from patients with underlying haematologic malignancies and favourable prognoses if aggressive supportive care is consistent with patient preferences.
Data collection for the ASH Research Collaborative COVID-19 Registry is ongoing and has been expanded to include non-malignant haematologic diseases. The Registry now supports batch data submissions from sites with high incidence of COVID-19.
- Wood WA, et al. Outcomes of Patients with Hematologic Malignancies and COVID-19 Infection: A Report from the ASH Research Collaborative Data Hub. 62nd ASH Annual Meeting, 5-8 December 2020. Abstract 215.
- Wood WA, et al. Blood Adv. 2020;4:5966-75.
Posted on
Previous Article
« Improved outcomes, but still substantial part experiences relapses Next Article
Allogeneic SARS-CoV-2-specific T cells to treat COVID-19 »
« Improved outcomes, but still substantial part experiences relapses Next Article
Allogeneic SARS-CoV-2-specific T cells to treat COVID-19 »
Table of Contents: ASH 2020
Featured articles
COVID-19
More complicated course of COVID-19 in leukaemia patients
Older age and imatinib treatment associated with COVID-19 mortality in CML
Allogeneic SARS-CoV-2-specific T cells to treat COVID-19
More severe COVID-19 outcomes for patients with haematologic malignancies
Acute Lymphoblastic Leukaemia
Improved outcomes, but still substantial part experiences relapses
Strong correlation between peripheral blood and bone marrow NGS MRD
Encouraging outcomes after autoHCT in patients with ALL
Acute Myeloid Leukaemia
Prognostic validity of AML composite model in predicting mortality
Venetoclax plus hypomethylating agents in favourable-risk AML
Encouraging clinical activity of decitabine plus ipilimumab in R/R or secondary MDS/AML
AML patients with specific mutations are unlikely to achieve MRD
Comparable outcomes with gilteritinib or quizartinib in R/R AML
First-in-class macrophage immune checkpoint inhibitor in AML
Bispecific DART® as salvage therapy for primary induction failure and early relapse
Gilteritinib in R/R AML patients priorly treated with midostaurin or sorafenib
Addition of venetoclax provides an effective, lower-intensity regimen
Chronic Leukaemia
Bosutinib effective and well tolerated in newly diagnosed CP-CML
Efficacy and safety of ponatinib in patients with CP-CML who failed second-generation TKIs
First-in-class STAMP inhibitor versus bosutinib in resistant or intolerant CML
PFS and ORR benefits of first-line ibrutinib-based treatment in CLL
Multiple Myeloma
Validation of MY-RADS response assessment category criteria
High symptom burden in transplant-ineligible patients with newly diagnosed MM
Added value of ixazomib to lenalidomide plus dexamethasone in transplant-ineligible newly diagnosed MM
Survival of transplant-eligible newly diagnosed MM in FORTE trial
Better survival with upfront autoSCT versus bortezomib-based intensification
Subcutaneous daratumumab plus pomalidomide and dexamethasone in R/R MM
Melflufen well tolerated with encouraging activity in heavily pretreated R/R MM
Initial data of FcRH5/CD3 T-cell-engaging bispecific antibody
Lymphoma
CD58 aberrations limit durable responses to CD19 CAR T-cell therapy
Anti-CD19 CAR T-cell therapy in relapsed/refractory indolent NHL
Myeloproliferative Neoplasms
MPN disease burden, quality of life, and treatment patterns
Interventions in JAK/STAT signalling pathway
Novel, orally available inhibitor of BCL-XL/BCL-2
New insights into genetics of MPN
Immune Thrombocytopenia
Mycophenolate efficacious and tolerable, even in elderly patients
First-in-class antibody sutimlimab selectively inhibits classical complement pathway
BTK inhibition provides clinically active and durable platelet response
Haemophilia, Sickle Cell Disease, Thalassaemia
First results from gene therapy trial in haemophilia B
Impact of haemophilia on children and their caregivers
Promising CRISPR gene editing results in β-thalassaemia and sickle cell disease
Erythroid maturation agent in patients with β-thalassaemia requiring regular RBC transfusions
Related Articles
February 18, 2021
First results from gene therapy trial in haemophilia B
February 18, 2021
New insights into genetics of MPN
© 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