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Utilization of anonymization techniques to create an external control arm for clinical trial data
BACKGROUND: Subject-level real-world data (RWD) collected during daily healthcare practices are increasingly used in medical research to assess questions that cannot be addressed in the context of a randomized controlled trial (RCT). A novel application of RWD arises from the need to create external...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10625188/ https://www.ncbi.nlm.nih.gov/pubmed/37925415 http://dx.doi.org/10.1186/s12874-023-02082-5 |
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author | Mehtälä, Juha Ali, Mehreen Miettinen, Timo Partanen, Liisa Laapas, Kaisa Niemelä, Petri T. Khorlo, Igor Ström, Sanna Kurki, Samu Vapalahti, Jarno Abdelgawwad, Khaled Leinonen, Jussi V. |
author_facet | Mehtälä, Juha Ali, Mehreen Miettinen, Timo Partanen, Liisa Laapas, Kaisa Niemelä, Petri T. Khorlo, Igor Ström, Sanna Kurki, Samu Vapalahti, Jarno Abdelgawwad, Khaled Leinonen, Jussi V. |
author_sort | Mehtälä, Juha |
collection | PubMed |
description | BACKGROUND: Subject-level real-world data (RWD) collected during daily healthcare practices are increasingly used in medical research to assess questions that cannot be addressed in the context of a randomized controlled trial (RCT). A novel application of RWD arises from the need to create external control arms (ECAs) for single-arm RCTs. In the analysis of ECAs against RCT data, there is an evident need to manage and analyze RCT data and RWD in the same technical environment. In the Nordic countries, legal requirements may require that the original subject-level data be anonymized, i.e., modified so that the risk to identify any individual is minimal. The aim of this study was to conduct initial exploration on how well pseudonymized and anonymized RWD perform in the creation of an ECA for an RCT. METHODS: This was a hybrid observational cohort study using clinical data from the control arm of the completed randomized phase II clinical trial (PACIFIC-AF) and RWD cohort from Finnish healthcare data sources. The initial pseudonymized RWD were anonymized within the (k, ε)-anonymity framework (a model for protecting individuals against identification). Propensity score matching and weighting methods were applied to the anonymized and pseudonymized RWD, to balance potential confounders against the RCT data. Descriptive statistics for the potential confounders and overall survival analyses were conducted prior to and after matching and weighting, using both the pseudonymized and anonymized RWD sets. RESULTS: Anonymization affected the baseline characteristics of potential confounders only marginally. The greatest difference was in the prevalence of chronic obstructive pulmonary disease (4.6% vs. 5.4% in the pseudonymized compared to the anonymized data, respectively). Moreover, the overall survival changed in anonymization by only 8% (95% CI 4–22%). Both the pseudonymized and anonymized RWD were able to produce matched ECAs for the RCT data. Anonymization after matching impacted overall survival analysis by 22% (95% CI -21–87%). CONCLUSIONS: Anonymization may be a viable technique for cases where flexible data transfer and sharing are required. As anonymization necessarily affects some aspects of the original data, further research and careful consideration of anonymization strategies are needed. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12874-023-02082-5. |
format | Online Article Text |
id | pubmed-10625188 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-106251882023-11-05 Utilization of anonymization techniques to create an external control arm for clinical trial data Mehtälä, Juha Ali, Mehreen Miettinen, Timo Partanen, Liisa Laapas, Kaisa Niemelä, Petri T. Khorlo, Igor Ström, Sanna Kurki, Samu Vapalahti, Jarno Abdelgawwad, Khaled Leinonen, Jussi V. BMC Med Res Methodol Research BACKGROUND: Subject-level real-world data (RWD) collected during daily healthcare practices are increasingly used in medical research to assess questions that cannot be addressed in the context of a randomized controlled trial (RCT). A novel application of RWD arises from the need to create external control arms (ECAs) for single-arm RCTs. In the analysis of ECAs against RCT data, there is an evident need to manage and analyze RCT data and RWD in the same technical environment. In the Nordic countries, legal requirements may require that the original subject-level data be anonymized, i.e., modified so that the risk to identify any individual is minimal. The aim of this study was to conduct initial exploration on how well pseudonymized and anonymized RWD perform in the creation of an ECA for an RCT. METHODS: This was a hybrid observational cohort study using clinical data from the control arm of the completed randomized phase II clinical trial (PACIFIC-AF) and RWD cohort from Finnish healthcare data sources. The initial pseudonymized RWD were anonymized within the (k, ε)-anonymity framework (a model for protecting individuals against identification). Propensity score matching and weighting methods were applied to the anonymized and pseudonymized RWD, to balance potential confounders against the RCT data. Descriptive statistics for the potential confounders and overall survival analyses were conducted prior to and after matching and weighting, using both the pseudonymized and anonymized RWD sets. RESULTS: Anonymization affected the baseline characteristics of potential confounders only marginally. The greatest difference was in the prevalence of chronic obstructive pulmonary disease (4.6% vs. 5.4% in the pseudonymized compared to the anonymized data, respectively). Moreover, the overall survival changed in anonymization by only 8% (95% CI 4–22%). Both the pseudonymized and anonymized RWD were able to produce matched ECAs for the RCT data. Anonymization after matching impacted overall survival analysis by 22% (95% CI -21–87%). CONCLUSIONS: Anonymization may be a viable technique for cases where flexible data transfer and sharing are required. As anonymization necessarily affects some aspects of the original data, further research and careful consideration of anonymization strategies are needed. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12874-023-02082-5. BioMed Central 2023-11-04 /pmc/articles/PMC10625188/ /pubmed/37925415 http://dx.doi.org/10.1186/s12874-023-02082-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Mehtälä, Juha Ali, Mehreen Miettinen, Timo Partanen, Liisa Laapas, Kaisa Niemelä, Petri T. Khorlo, Igor Ström, Sanna Kurki, Samu Vapalahti, Jarno Abdelgawwad, Khaled Leinonen, Jussi V. Utilization of anonymization techniques to create an external control arm for clinical trial data |
title | Utilization of anonymization techniques to create an external control arm for clinical trial data |
title_full | Utilization of anonymization techniques to create an external control arm for clinical trial data |
title_fullStr | Utilization of anonymization techniques to create an external control arm for clinical trial data |
title_full_unstemmed | Utilization of anonymization techniques to create an external control arm for clinical trial data |
title_short | Utilization of anonymization techniques to create an external control arm for clinical trial data |
title_sort | utilization of anonymization techniques to create an external control arm for clinical trial data |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10625188/ https://www.ncbi.nlm.nih.gov/pubmed/37925415 http://dx.doi.org/10.1186/s12874-023-02082-5 |
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