» Articles » PMID: 35222045

Real World Data in Health Technology Assessment of Complex Health Technologies

Overview
Journal Front Pharmacol
Date 2022 Feb 28
PMID 35222045
Authors
Affiliations
Soon will be listed here.
Abstract

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 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.

Citing Articles

From Vision to Reality: The EU's Pharmaceutical Reforms and the Path to Improved Access.

Main C, Schafer C, Kanavos P Pharmacoecon Open. 2025; .

PMID: 39862340 DOI: 10.1007/s41669-024-00556-w.


Use of transportability methods for real-world evidence generation: a review of current applications.

Levy N, Arena P, Jemielita T, Mt-Isa S, McElwee S, Lenis D J Comp Eff Res. 2024; 13(11):e240064.

PMID: 39364567 PMC: 11542082. DOI: 10.57264/cer-2024-0064.


The potential role of real-world evidence in Centers for Medicare & Medicaid Services' future price negotiations: Recommendations for a robust framework.

Jaksa A, Arena P J Manag Care Spec Pharm. 2024; 30(6):604-607.

PMID: 38824624 PMC: 11145000. DOI: 10.18553/jmcp.2024.30.6.604.


Suitability of the Current Health Technology Assessment of Innovative Artificial Intelligence-Based Medical Devices: Scoping Literature Review.

Farah L, Borget I, Martelli N, Vallee A J Med Internet Res. 2024; 26:e51514.

PMID: 38739911 PMC: 11130781. DOI: 10.2196/51514.


Cross-sectional analysis of use of real-world data in single technology appraisals of oncological medicine by the National Institute for Health and Care Excellence in 2011-2021.

Kang J, Cairns J BMJ Open. 2024; 14(3):e077297.

PMID: 38485485 PMC: 10941141. DOI: 10.1136/bmjopen-2023-077297.


References
1.
Collins R, Bowman L, Landray M, Peto R . The Magic of Randomization versus the Myth of Real-World Evidence. N Engl J Med. 2020; 382(7):674-678. DOI: 10.1056/NEJMsb1901642. View

2.
Kesselheim A, Wang B, Franklin J, Darrow J . Trends in utilization of FDA expedited drug development and approval programs, 1987-2014: cohort study. BMJ. 2015; 351:h4633. PMC: 4580726. DOI: 10.1136/bmj.h4633. View

3.
Makady A, van Veelen A, Jonsson P, Moseley O, dAndon A, de Boer A . Using Real-World Data in Health Technology Assessment (HTA) Practice: A Comparative Study of Five HTA Agencies. Pharmacoeconomics. 2017; 36(3):359-368. PMC: 5834594. DOI: 10.1007/s40273-017-0596-z. View

4.
Justo N, Espinoza M, Ratto B, Nicholson M, Rosselli D, Ovcinnikova O . Real-World Evidence in Healthcare Decision Making: Global Trends and Case Studies From Latin America. Value Health. 2019; 22(6):739-749. DOI: 10.1016/j.jval.2019.01.014. View

5.
Vreman R, Naci H, Goettsch W, Mantel-Teeuwisse A, Schneeweiss S, Leufkens H . Decision Making Under Uncertainty: Comparing Regulatory and Health Technology Assessment Reviews of Medicines in the United States and Europe. Clin Pharmacol Ther. 2020; 108(2):350-357. PMC: 7484915. DOI: 10.1002/cpt.1835. View