From the Journals

FVIII/W ratio may help predict relapse in hemophilia A


 

FROM HAEMOPHILIA

The FVIII/W (factor VIII:C/von Willebrand factor antigen) ratio appears to be a reliable biological marker to predict recovery and/or relapse in patients with acquired hemophilia A, according to a retrospective analysis.

Marc Trossaert, MD, PhD, of the CHU de Nantes, France, and colleagues conducted a retrospective analysis of 64 consecutive patients diagnosed with acquired hemophilia A over a period of 15 years (2000-2015). Data were obtained from institutional databases at the Toulouse and Nantes university hospitals in France.

Data collected included patient demographics, comorbidities, biological factors, and information related to immunosuppressive therapy. The findings of the study were published in Haemophilia.

To ascertain normal parameters and uses of the FVIII/W ratio, the team assessed FVIII:C and VWF:Ag levels of 40 healthy individuals and normal parameters of the ratio were defined using these levels.

Among the 64 patients with acquired hemophilia A who were enrolled in the study, 55 patients achieved complete remission. Of that group, 44 patients did not relapse. Researchers had follow-up data of at least 1 year for 22 of these patients. They found that the FVIII/W ratio remained within normal parameters for all 22 patients.

Researchers had follow-up data on 5 of the 11 patients who relapsed during the study period. For 4 of the patients, a decrease of FVIII/W ratio was the first indicator of relapse. In the fifth patient, an abnormal activated partial thromboplastin time (aPTT) displayed before the changes were observed in the FVIII/W ratio.

Dr. Trossaert and his colleagues acknowledged that a key limitation of the study was the retrospective design.

“We cannot eliminate the fact that in these patients less frequent testing may have influenced the chance of seeing a low FVIII/W ratio,” they wrote.

The biomarker now needs to be studied in larger cohorts, the researchers suggested.

No funding sources were reported. The authors reported having no conflicts of interest.

SOURCE: Trossaert M et al. Haemophilia. 2019 May 2. doi: 10.1111/hae.13752.

Recommended Reading

TTP death linked to elevated troponin and neurological signs
MDedge Hematology and Oncology
LentiGlobin reduces transfusion dependence in young thalassemia patients
MDedge Hematology and Oncology
Study identifies GI bleed risk factors in von Willebrand disease
MDedge Hematology and Oncology
New recommendations on immune tolerance induction in hemophilia A
MDedge Hematology and Oncology
Study finds lower quality of life for patients with hemophilia A
MDedge Hematology and Oncology
QOL concerns prompt second-line therapy in children with ITP
MDedge Hematology and Oncology
Peanut contamination risk prompts Promacta recall
MDedge Hematology and Oncology
Family history plays a large role in bleeding disorder diagnosis in women
MDedge Hematology and Oncology
Low-dose FVIII prophylaxis reduced bleeding in hemophilia A
MDedge Hematology and Oncology
Novel chromogenic assay looks accurate in hemophilia A diagnosis
MDedge Hematology and Oncology