Publications by authors named "J S H Curnow"

This perspective discusses the critical role of laboratory assessments in assessing factor VIII (FVIII) inhibitors. These are auto- and alloantibodies that can develop against both endogenous and exogenous FVIII, respectively. Assessment for inhibitors represents a key part of the management of both congenital hemophilia A (CHA), an inherited deficiency, and acquired hemophilia A (AHA), an autoimmune condition.

View Article and Find Full Text PDF
Article Synopsis
  • Von Willebrand disease (VWD) is the most common inherited bleeding disorder caused by issues with von Willebrand factor (VWF), often leading to misdiagnosis and improper management.
  • Treatment mainly involves replacing the deficient or defective VWF, with additional therapies tailored to specific patient needs, including new treatment options like FVIII replacement and antibody-based strategies.
  • The future of VWD treatment is expected to evolve significantly with personalized approaches, offering tailored therapies based on individual patient circumstances and treatment goals.
View Article and Find Full Text PDF
Article Synopsis
  • The NHL29 trial evaluated the effectiveness of combining ibrutinib with R-mini-CHOP chemotherapy in patients over 75 with newly diagnosed diffuse large B-cell lymphoma (DLBCL).
  • Results showed a 2-year overall survival rate of 68% and a progression-free survival rate of 60%, with an overall response rate of 76%.
  • Despite some serious adverse events, including infections and diarrhea, improvements in health-related quality of life were noted among responders, indicating the treatment's viability for elderly patients.
View Article and Find Full Text PDF

Measurable residual disease (MRD) is useful for prognostication and for monitoring response to treatment in patients with acute leukaemia. MRD by multiparametric flow cytometry (MFC-MRD) utilises the leukaemia-associated immunophenotype (LAIP) and difference from normal (DfN) strategies to identify the leukaemic clone. Difficulties arise when the LAIP overlaps with normal regeneration, there is clonal evolution, or when the abnormal clone population is exceptionally small e.

View Article and Find Full Text PDF

Background: High/intermediate-risk pulmonary embolism (PE) confers increased risk of cardiovascular morbidity and mortality. International guidelines recommend the formation of a PE response team (PERT) for PE management because of the complexity of risk stratification and emerging treatment options. However, there are currently no available Australian data regarding outcomes of PE managed through a PERT.

View Article and Find Full Text PDF