Dr Annoek Broers (Erasmus MC Cancer Institute, the Netherlands) presented the study [1]. She noted that GVHD is the major cause of morbidity and mortality after allogeneic haematopoietic stem cell transplantation. Thus, HOVON-96 investigators developed a multicentre, randomised, prospective trial to compare post-transplantation cyclophosphamide with conventional immunosuppression in patients qualifying for allogeneic haematopoietic stem cell transplantation using grafts from HLA-matched siblings and unrelated donors.
HOVON-96 randomly assigned 160 patients 1:2 to either conventional immunosuppression with cyclosporine from days -3 to +180 plus mycophenolic acid from days 0 to +84 or post-transplantation cyclophosphamide with cyclosporine from days +5 to +70 plus cyclophosphamide at 50 mg/kg on days +3 and +4. The composite of GVHD-free/relapse-free survival was defined as the absence of acute GVHD grade 3-4 and chronic GVHD requiring systemic immunosuppression, plus disease relapse and death. The median follow-up was 38.7 months.
Transplantation was completed by 151 patients with high-risk haematologic malignancies and a related or unrelated donor with a 10 of 10 HLA match. Myeloablative conditioning was performed in 2 patients. The donor type was matched related in 31% and matched unrelated in 69% of patients. Transplants were derived from peripheral blood in 97% of patients and consisted of a median 6.14 x 106/kg CD34-positive cells/kg and a median 230 x 106/kg CD3-positive T cells. Baseline characteristics were comparable between the arms.
The composite endpoint, GVHD-free/relapse-free survival, was 22% with conventional prophylaxis compared with 45% with post-transplant cyclophosphamide—a 50% reduction in risk (P=0.001). Furthermore, post-transplantation cyclophosphamide versus conventional immunosuppression reduced the incidence of acute grades 2-4 GVHD: 32% versus 48% (P=0.014), respectively. Similarly, researchers reported reduced incidence of chronic GVHD: 19% versus 50% (P=0.001), respectively. However, no differences were observed in non-relapse mortality (P=0.54), progression-free survival (P=0.67) or overall survival (P=0.63).
Grade 3 or 4 adverse events were observed in 60% of the experimental arm and 42% of the conventional arm. There were more infections with cyclophosphamide (41% vs 21%, respectively) and neutropenic fever (25% vs 15%, respectively). Cardiac toxicity was rare, seen in just 1 patient (1%) in the cyclophosphamide arm and 2 patients (4%) in the conventional arm. There were also 2 graft failures, 1 in each arm.
1. De Jong CN, et al. Abstract 1, ASH 2019, 7-10 December, Oralando, USA.
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Table of Contents: ASH 2019
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Late-Breaking Abstracts
Likely new standard of care: Blinatumomab for children with relapsed B-ALL
Pivotal phase 3 trial in cold agglutinin disease: sutimlimab can stop haemolysis
Oral azacitidine improves overall survival in patients with AML in remission
BCL11A as a novel target in gene therapy for sickle cell disease
Adding daratumumab to carfilzomib/dexamethasone prolongs PFS and OS in R/R MM
Long-term data of ropeginterferon alpha-2b in polycythaemia vera
Anti-CD70 is safe with hypomethylating agents in AML
MRD assessment to guide pre-emptive treatment decisions
Luspatercept effective for myelofibrosis-associated anaemia
Arsenic, ATRA, and ascorbic acid in acute promyelocytic leukaemia maintenance
Updated results ECOG-ACRIN E2906: decitabine maintenance after alloSCT
Sickle Cell Disease
Arginine supplements help against sickle cell disease pain
Abatacept prevents graft-versus-host disease in sickle cell patients after alloSCT
Plenary Scientific Session
HOVON-96: Better outcomes with cyclophosphamide after transplantation
Erythroferrone and skeletal changes associated with thalassaemia
Experimental model for limitations of haematopoietic stem cells propagation
Mosunetuzumab: complete remissions in non-Hodgkin lymphoma
Inclusive Medicine
Socioeconomic disparities and survival in paediatric AML
Oral selinexor/pomalidomide/dexamethasone shows activity in heavily pre-treated multiple myeloma
CAR T-cell therapy successful in older non-Hodgkin’s lymphoma patients
Mild renal impairment in African Americans does not affect OS in AML
ALCYONE: New overall survival results for myeloma
Venous Thromboembolism
Rivaroxaban is safe and effective for paediatric venous thromboembolism
Aspirin plus DOAC is not better than a DOAC alone
20-Year follow-up of imatinib in chronic myeloid leukaemia after failure with interferon
CAR T and Beyond
BCMA-targeted CAR T therapy yields 100% response in relapsed/refractory MM
Anti-BCMA/anti-CD38 in refractory multiple myeloma
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