TY - JOUR
T1 - Real World Data in Health Technology Assessment of Complex Health Technologies
AU - Hogervorst, Milou A
AU - Pontén, Johan
AU - Vreman, Rick A
AU - Mantel-Teeuwisse, Aukje K
AU - Goettsch, Wim G
N1 - Funding Information:
This research was performed as part of the HTx project. The project has received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement No 825162. This dissemination reflects only the author’s view and the Commission is not responsible for any use that may be made of the information it contains.
Funding Information:
Data were collected through dissemination of a questionnaire. This strategy allowed us to gain insight in daily practice in HTA organizations. The questions on RWD were combined with questions informing additional deliverables in the HTx project, all focusing on complex treatments. The HTx project is a Horizon 2020 project supported by the European Union lasting for 5 years from January 2019, with the aim to create a framework for the Next Generation HTA to support patient-centered, societally oriented, real-time decision-making on access to and reimbursement for health technologies throughout Europe (HTx, 2020). The broad definition for RWD that we used was ‘all routinely collected data on patients that are not RCTs’ (Makady et al., 2017b). A full description of the methods on the questionnaire’s development, validation and dissemination is published in an earlier study (Hogervorst et al., 2021).
Publisher Copyright:
Copyright © 2022 Hogervorst, Pontén, Vreman, Mantel-Teeuwisse and Goettsch.
PY - 2022/2/10
Y1 - 2022/2/10
N2 - The available evidence on relative effectiveness and risks of new health technologies is often limited at the time of health technology assessment (HTA). Additionally, a wide variety in real-world data (RWD) policies exist among HTA organizations. This study assessed which challenges, related to the increasingly complex nature of new health technologies, make the acceptance of RWD most likely. A questionnaire was disseminated among 33 EUnetHTA member HTA organizations. The questions focused on accepted data sources, circumstances that allowed for RWD acceptance and barriers to acceptance. The questionnaire was validated and tested for reliability by an expert panel, and pilot-tested before dissemination
via LimeSurvey. Twenty-two HTA organizations completed the questionnaire (67%). All reported accepting randomized clinical trials. The most accepted RWD source were patient registries (19/22, 86%), the least accepted were editorials and expert opinions (8/22, 36%). With orphan treatments or companion diagnostics, organizations tended to be most likely to accept RWD sources, 4.3-3.2 on a 5-point Likert scale, respectively. Additional circumstances were reported to accept RWD (e.g., a high disease burden). The two most important barriers to accepting RWD were lacking necessary RWD sources and existing policy structures. European HTA organizations seem positive toward the (wider) use of RWD in HTA of complex therapies. Expanding the use of patient registries could be potentially useful, as a large share of the organizations already accepts this source. However, many barriers still exist to the widespread use of RWD. Our results can be used to prioritize circumstances in which RWD might be accepted.
AB - The available evidence on relative effectiveness and risks of new health technologies is often limited at the time of health technology assessment (HTA). Additionally, a wide variety in real-world data (RWD) policies exist among HTA organizations. This study assessed which challenges, related to the increasingly complex nature of new health technologies, make the acceptance of RWD most likely. A questionnaire was disseminated among 33 EUnetHTA member HTA organizations. The questions focused on accepted data sources, circumstances that allowed for RWD acceptance and barriers to acceptance. The questionnaire was validated and tested for reliability by an expert panel, and pilot-tested before dissemination
via LimeSurvey. Twenty-two HTA organizations completed the questionnaire (67%). All reported accepting randomized clinical trials. The most accepted RWD source were patient registries (19/22, 86%), the least accepted were editorials and expert opinions (8/22, 36%). With orphan treatments or companion diagnostics, organizations tended to be most likely to accept RWD sources, 4.3-3.2 on a 5-point Likert scale, respectively. Additional circumstances were reported to accept RWD (e.g., a high disease burden). The two most important barriers to accepting RWD were lacking necessary RWD sources and existing policy structures. European HTA organizations seem positive toward the (wider) use of RWD in HTA of complex therapies. Expanding the use of patient registries could be potentially useful, as a large share of the organizations already accepts this source. However, many barriers still exist to the widespread use of RWD. Our results can be used to prioritize circumstances in which RWD might be accepted.
KW - Europe
KW - complex health technologies
KW - health technology assessment
KW - questionnaire
KW - real-world data
UR - http://www.scopus.com/inward/record.url?scp=85125300527&partnerID=8YFLogxK
U2 - 10.3389/fphar.2022.837302
DO - 10.3389/fphar.2022.837302
M3 - Article
C2 - 35222045
SN - 1663-9812
VL - 13
SP - 1
EP - 9
JO - Frontiers in Pharmacology
JF - Frontiers in Pharmacology
M1 - 837302
ER -