Original Articles

Development of a shared decision-making tool for gene therapy in hemophilia A in Italy

Publisher's note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
Published: 22 June 2026
0
Views
0
Downloads

Authors

Background: Gene therapy offers a transformative treatment option for hemophilia A (HA) by restoring endogenous factor VIII production. Shared decision-making (SDM) is a collaborative process that allows patients and clinicians to weigh the risks and benefits of complex treatment options such as gene therapy. However, no SDM tools exist for the specific needs of Italian persons with HA.

Materials and Methods: An Expert Advisory Board comprising nine experts (including hematologists, a psychologist, a methodology expert, a linguist and patient advocacy group representatives) met three times between March and July 2024 to discuss gene therapy for HA in Italy, and develop an SDM tool to determine the suitability of gene therapy for HA.

Results: The resulting modular SDM tool allows for structured interactions between clinicians and patients, while remaining sensitive to each patient’s level of readiness and understanding. The tool includes three components: Role Definition, Agenda Alignment, and Intention Setting, with supporting materials to guide patient-clinician dialogue and various resources (questionnaires, brochures, and visual aids).

Conclusions: Despite requiring confirmation in further studies, this SDM tool may represent a useful component of patient-centered care for HA in the Italian healthcare setting.

Downloads

Download data is not yet available.

Citations

1. Berntorp E, Fischer K, Hart DP, et al. Haemophilia. Nat Rev Dis Primers 2021;7:45. DOI: https://doi.org/10.1038/s41572-021-00278-x
2. Iorio A, Stonebraker JS, Chambost H, et al. Establishing the prevalence and prevalence at birth of hemophilia in males: a meta-analytic approach using national registries. Ann Intern Med 2019;171:540-6. DOI: https://doi.org/10.7326/M19-1208
3. Valentino LA, Blanchette V, Negrier C, et al. Personalising haemophilia management with shared decision making. J Haem Pract 2021;8:69-79. DOI: https://doi.org/10.17225/jhp00178
4. O'Hara J, Hughes D, Camp C, et al. The cost of severe haemophilia in Europe: the CHESS study. Orphanet J Rare Dis 2017;12:106. DOI: https://doi.org/10.1186/s13023-017-0660-y
5. Hermans C, Gruel Y, Frenzel L, et al. How to translate and implement the current science of gene therapy into haemophilia care? Ther Adv Hematol 2023;14:20406207221145627. DOI: https://doi.org/10.1177/20406207221145627
6. Ozelo MC, Mahlangu J, Pasi KJ, et al. Valoctocogene roxaparvovec gene therapy for hemophilia A. N Engl J Med 2022;386:1013-25. DOI: https://doi.org/10.1056/NEJMoa2113708
7. European Medicines Agency. Roctavian: EPAR - Product Information. European Medicines Agency; 2022. Available from: https://www.ema.europa.eu/en/medicines/human/EPAR/roctavian (accessed: October 8, 2024).
8. Leavitt AD, Mahlangu J, Raheja P, et al. Durability of efficacy, safety, and quality of life 5 years after valoctocogene roxaparvovec gene transfer for severe hemophilia A: final phase 3 GENEr8-1 trial results. Res Practice Thrombosis Haemostasis 2026;10:103416. DOI: https://doi.org/10.1016/j.rpth.2026.103416
9. Elwyn G, Laitner S, Coulter A, et al. Implementing shared decision making in the NHS. BMJ 2010;341:c5146. DOI: https://doi.org/10.1136/bmj.c5146
10. Epstein RM, Gramling RE. What is shared in shared decision making? Complex decisions when the evidence is unclear. Med Care Res Rev 2013;70:94s-112s. DOI: https://doi.org/10.1177/1077558712459216
11. Wang M, Negrier C, Driessler F, et al. The hemophilia gene therapy patient journey: questions and answers for shared decision-making. Patient Prefer Adherence 2022;16:1439-47. DOI: https://doi.org/10.2147/PPA.S355627
12. Stiggelbout AM, Pieterse AH, De Haes JC. Shared decision making: concepts, evidence, and practice. Patient Educ Couns 2015;98:1172-9. DOI: https://doi.org/10.1016/j.pec.2015.06.022
13. Hughes TM, Merath K, Chen Q, et al. Association of shared decision-making on patient-reported health outcomes and healthcare utilization. Am J Surg 2018;216:7-12. DOI: https://doi.org/10.1016/j.amjsurg.2018.01.011
14. Anderson G, Rega ML, Casasanta D, et al. The association between patient activation and healthcare resources utilization: a systematic review and meta-analysis. Public Health 2022;210:134-41. DOI: https://doi.org/10.1016/j.puhe.2022.06.021
15. Muscat DM, Shepherd HL, Nutbeam D, et al. Health literacy and shared decision-making: exploring the relationship to enable meaningful patient engagement in healthcare. J Gen Intern Med 2021;36:521-4. DOI: https://doi.org/10.1007/s11606-020-05912-0
16. Athale A, Giguere A, Barbara A, et al. Developing a two-sided intervention to facilitate shared decision-making in haemophilia: decision boxes for clinicians and patient decision aids for patients. Haemophilia 2014;20:800-6. DOI: https://doi.org/10.1111/hae.12495
17. Lanzel AF, Soucie JM, Meeks SL, et al. Ethical decision making framework in previously untreated severe hemophilia A patients. Blood 2017;130:5583.
18. Hermans C, Noone D, Benson G, et al. Hemophilia treatment in 2021: choosing the"optimal" treatment using an integrative, patient-oriented approach to shared decision-making between patients and clinicians. Blood Rev 2022;52:100890. DOI: https://doi.org/10.1016/j.blre.2021.100890
19. Limjoco J, Thornburg CD. Development of a haemophilia A gene therapy shared decision-making tool for clinicians. Haemophilia 2023;29:1184-90. DOI: https://doi.org/10.1111/hae.14822
20. Di Minno G, Spadarella G, Maldonato NM, et al. Awareness of individual goals, preferences, and priorities of persons with severe congenital haemophilia A for a tailored shared decision-making approach to liver-directed gene therapy. A practical guideline. Blood Rev 2023;62:101118. DOI: https://doi.org/10.1016/j.blre.2023.101118
21. Meade L, Klaassen R, Sun HL, et al. Enhancing engagement to support shared decision-making within haemophilia. Haemophilia 2023;29:196-7.
22. Roberts JC, Richardson S, Miles ME, et al. The GOAL-Hēm journey: shared decision making and patient-centred outcomes. Haemophilia 2022;28:784-95. DOI: https://doi.org/10.1111/hae.14608
23. Coffin D, Skinner MW, Thornburg CD, et al. Development of the World Federation of Hemophilia Shared Decision-Making Tool. Haemophilia 2024;30:1298-308. DOI: https://doi.org/10.1111/hae.15100
24. Sun HL, Klaassen RJ, Anger DL, et al. Shared decision-making related to treatment of haemophilia: a scoping review of influential factors and available support tools. Haemophilia 2024;30:880-93. DOI: https://doi.org/10.1111/hae.15026
25. Di Minno G, Spadarella G, Calcaterra IL, et al. The evolving landscape of gene therapy for congenital severe hemophilia: a 2024 state of the art. Bleeding Thromb Vasc Biol 2024;3:144. DOI: https://doi.org/10.4081/btvb.2024.144
26. Pierce GF, Coffin D. The 1st WFH Gene Therapy Round Table: understanding the landscape and challenges of gene therapy for haemophilia around the world. Haemophilia 2019;25:189-94. DOI: https://doi.org/10.1111/hae.13673
27. Peyvandi F, Lillicrap D, Mahlangu J, et al. Hemophilia gene therapy knowledge and perceptions: results of an international survey. Res Pract Thromb Haemost 2020;4: 644-51. DOI: https://doi.org/10.1002/rth2.12326
28. Cutica I, Mortarino M, Garagiola I, et al. Knowledge and attitudes toward gene therapy of a cohort of Italian patients with hemophilia. J Thromb Haemost 2024;22:1001-8. DOI: https://doi.org/10.1016/j.jtha.2023.12.018
29. Solari A, Giordano A, Kasper J, et al. Role preferences of people with multiple sclerosis: image-revised, computerized self-administered version of the control preference scale. PLoS One 2013;8:e66127. DOI: https://doi.org/10.1371/journal.pone.0066127
30. Arnett GW, Worley CM, Jr. The Treatment Motivation Survey: defining patient motivation for treatment. Am J Orthod Dentofacial Orthop 1999;115:233-8. DOI: https://doi.org/10.1016/S0889-5406(99)70323-9
31. Shedden-Mora MC, Alberts J, Petrie KJ, et al. The Treatment Expectation Questionnaire (TEX-Q): validation of a generic multidimensional scale measuring patients' treatment expectations. PLoS One 2023;18:e0280472. DOI: https://doi.org/10.1371/journal.pone.0280472

Ethics Approval

GDM was a speaker or a member of a speaker bureau for BioMarin and CSL Behring; and was an ad-hoc speaker/consultant for BioMarin and CSL Behring. SBi and SBa have acted as consultants for BioMarin. EFG participated in speakers’ bureaus on behalf of a patient organization for BioMarin, CSL Behring, Novo Nordisk, Roche, and Sobi; participated in advisory boards on behalf of a patient organization for BioMarin, Pfizer, Roche, and Sobi; and participated in patient councils on behalf of a patient organization for BioMarin, Novo Nordisk, and Roche. MF has no competing interests to declare. MFM has acted as consultant and discus-sant for BioMarin, Novo Nordisk, Roche, and Sobi. MN has acted as consultant for Amgen, Bayer, CSL Behring, and Novo Nordisk; and received speaker fees from Amgen, Bayer, CSL Behring, Novartis, Novo Nordisk, Sanofi Genzyme, Sobi, and Takeda. RCS has acted as con-sultant for Bayer, Novo Nordisk, Roche, Sobi, and Takeda; and received speaker fees from Bayer, BioMarin, CSL Behring, Novo Nordisk, Kedrion, Roche, Sobi, and Takeda. GC received pay-ment or honoraria for lectures, presentations, speakers’ bureaus or educational events from Bi-oMarin, Bioviiix, CSL Behring, Kedrion, LFB, Novo Nordisk, Roche, Sanofi, Sobi, and Takeda, and participated on a Data Safety Monitoring Board or Advisory Board for Bayer, BioMarin, CSL Behring, Kedrion, LFB, Novo Nordisk, Pfizer, Roche, Sanofi, and Takeda

CRediT authorship contribution

GDM, SBi, SBa, and GC contributed to developing the manuscript concept and plan; EFG, MF, MFM, MN, and RCS contributed to manuscript writing and editing. All the au-thors read and approved the final version of the manuscript and agreed to be accountable for all aspects of the work. Artificial intelligence (AI)-assisted technologies were not used in the creation of the submitted work.

Supporting Agencies

This project, the development of the manuscript and the open access publishing fee were supported by BioMarin, without conditions.

How to Cite



1.
Di Minno G, Bigi S, Barello S, Ferri Grazzi E, Follino M, Mansueto MF, et al. Development of a shared decision-making tool for gene therapy in hemophilia A in Italy. Bleeding Thromb Vasc Biol [Internet]. 2026 Jun. 22 [cited 2026 Jun. 23];5(2). Available from: https://www.btvb.org/btvb/article/view/426

Most read articles by the same author(s)

1 2 > >>