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Venous Thromboembolism in Children: The Rivaroxaban Experience
Luca Spiezia1, Elena Campello1, Daniela Tormene1
1General Internal Medicine and Thrombotic and Haemorrhagic Diseases Unit, Department of Medicine, Padova University School of Medicine, Padova, Italy.
Insights
Pediatric venous thromboembolism (VTE) management is challenging. Rivaroxaban oral suspension offers a safe and effective oral treatment option for children, supported by robust clinical trial data.
Area of Science:
- Pediatric Hematology
- Pharmacology and Therapeutics
- Clinical Trial Research
Background:
- Pediatric venous thromboembolism (VTE) incidence has significantly increased.
- Current VTE treatments in children involve cumbersome parenteral medications and frequent blood tests.
- There is a need for safe, effective, and orally administered anticoagulants for pediatric use.
Purpose of the Study:
- To evaluate the efficacy and safety of rivaroxaban oral suspension in pediatric patients.
- To establish appropriate dosing schedules for rivaroxaban in children using pharmacokinetic modeling.
- To review the clinical evidence supporting rivaroxaban use in various pediatric VTE scenarios.
Main Methods:
- Development of a physiologically based pharmacokinetic model incorporating pediatric growth and maturation.
- Conduct of a comprehensive investigational program including Phase I, II, and III clinical trials.
- The Phase III EINSTEIN JUNIOR trial enrolled 500 pediatric patients (birth to <18 years).
Main Results:
- Rivaroxaban demonstrated efficacy and safety profiles comparable to adult studies in the pediatric population.
- Dosing regimens were established to be equivalent to the adult 20 mg dose.
- Results support rivaroxaban's use for preventing recurrent VTE and managing major bleeding in children.
Conclusions:
- Rivaroxaban oral suspension is a safe and effective oral treatment for pediatric VTE.
- Clinical evidence supports its use across diverse pediatric patient populations and vascular beds.
- Rivaroxaban offers a beneficial alternative to traditional parenteral anticoagulants in children.
Abstract:
The incidence of venous thromboembolism (VTE) in the pediatric population has increased more than 10-fold in the last 20 years, as a consequence of the advancement of resuscitation and surgical techniques and the global increase in life expectancy of children suffering from chronic pathologies. Monitoring anticoagulant therapy to achieve outcomes within the target range in childhood VTE, parenteral administration of medications, and frequent blood tests in children are often cumbersome. Availability of safe and effective oral agents with pediatric data to support use would be of clear benefit. A physiologically based pharmacokinetic model was developed to estimate the appropriate dosing schedule for rivaroxaban in children. This incorporated growth/maturation and variability in anthropometrics (e.g., body height, weight, and body mass index), anatomy (e.g., organ weight), physiology (e.g., blood flow rates), metabolism and excretion. Rivaroxaban use in pediatric population underwent a complete investigational program, consisting mainly of one phase I pharmacokinetics/pharmacodynamics trial, three phase II trials, one phase III trial. The phase III trial enrolled 500 patients from birth to <18 years and documented the efficacy and safety of rivaroxaban regimens at dose equivalent to the adult 20 mg dose for the prevention of fatal or symptomatic nonfatal recurrent VTE and major bleeding versus heparin or vitamin K antagonists. Results were similar to those in rivaroxaban studies in adults. The efficacy and safety of rivaroxaban in children reported in the EINSTEIN JUNIOR trial provide further support to previous trials in adults (EINSTEIN Program), which demonstrate a favorable profile for the use of rivaroxaban for the management of VTE in challenging patient populations. Other clinical evidence contributing to the use of rivaroxaban among different risk groups in pediatric VTE population confirms the consistency with principal trial. Our review aims to describe the rationale for using rivaroxaban oral suspension in clinical practice and to summarize its multiple indications in each vascular bed (e.g., cerebral venous thrombosis, symptomatic or asymptomatic central venous catheter-associated thrombosis), etiology, and patients setting.
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