# Health care resources and costs associated with delivering gene therapy for hemophilia in clinical practice

**Authors:** Diaz M. Prameyllawati, Caroline M.A. Mussert, Martijn A.H. Oude Voshaar, Hester F. Lingsma, Marjon H. Cnossen, Michiel Coppens, Karina Meijer, Paul R. van der Valk, Frank W.G. Leebeek, Renske M.T. ten Ham

PMC · DOI: 10.1016/j.rpth.2025.103275 · Research and Practice in Thrombosis and Haemostasis · 2025-12-02

## TL;DR

This study estimates the healthcare resources and costs of delivering gene therapy for hemophilia in real-world clinical settings.

## Contribution

The study provides the first real-world cost estimates for hemophilia gene therapy delivery using a bottom-up microcosting approach.

## Key findings

- Estimated total costs for hemophilia A and B gene therapy delivery are €28,696 and €20,511 per individual, respectively.
- Resource use includes personnel time, hospital visits, laboratory tests, and medical consumables.

## Abstract

The debate around the cost-effectiveness of gene therapy for hemophilia has largely centered on its price (€1-€3.5 million per individual). While previous studies have explored care organization for gene therapy delivery, none have evaluated the potential resource utilization and associated costs in a real-world setting.

This study aimed to estimate the health care resources and costs of delivering gene therapy for hemophilia in clinical practice.

We conducted a bottom-up microcosting study and constructed a process map outlining each step of care. Data on resource use were obtained from clinical trial protocols and translated to reflect real-world clinical practice through semistructured interviews. Dutch unit costs were assigned to each resource, and mean total costs per individual were calculated for hemophilia A and B. Sensitivity analyses were performed to assess the potential range of consumed resources and costs.

In clinical practice, delivering gene therapy for hemophilia is expected to require resources such as personnel time, hospital visits, laboratory tests, liver function assessments, drugs, hospital facilities, medical consumables, and office equipment. The estimated total cost for an eligible individual without liver function abnormalities, covering screening, pretreatment preparation, administration, and first-year follow-up, is €28,696 (€20,873-€48,973) for hemophilia A and €20,511 (€18,175-€36,310) for hemophilia B.

Delivery of hemophilia gene therapy requires significant resources, incurs substantial costs, and demands additional organizational infrastructure within treatment facilities. These findings may aid stakeholders to better plan implementation of these innovative therapies into clinical practice, as well as inform economic evaluations and reimbursement discussions.

•Implementing gene therapy for hemophilia in clinical practice may incur notable delivery costs.•This microcosting study combined trial data with expert interviews to estimate delivery costs.•Estimated delivery costs on average: €28,696 (hemophilia A) and €20,511 (hemophilia B).•Our findings inform clinical implementation, economic evaluations, and reimbursement discussions.

Implementing gene therapy for hemophilia in clinical practice may incur notable delivery costs.

This microcosting study combined trial data with expert interviews to estimate delivery costs.

Estimated delivery costs on average: €28,696 (hemophilia A) and €20,511 (hemophilia B).

Our findings inform clinical implementation, economic evaluations, and reimbursement discussions.

## Linked entities

- **Diseases:** hemophilia (MONDO:0018660)

## Full-text entities

- **Diseases:** liver function abnormalities (MESH:D056486), hemophilia A and B. (MESH:D002836), hemophilia (MESH:D006467)

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12800355/full.md

## References

49 references — full list in the complete paper: https://tomesphere.com/paper/PMC12800355/full.md

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Source: https://tomesphere.com/paper/PMC12800355