A structured approach for data collection and visualization of the International Childhood Cancer Core Outcomes

<h2>Abstract</h2><h3>Background</h3> Insight into clinically relevant outcomes for children with cancer is crucial for improving treatment and follow-up strategies. The International Childhood Cancer Core Outcome Project developed a harmonized core outcome set, involving patients and providers across all types of childhood cancer. <h3>Objective</h3> This paper highlights the strategy used at the Princess Máxima Center for pediatric oncology for the collection and visualization of the International Childhood Cancer Core Outcomes. <h3>Project phases</h3> In phase 1, we created an overview of data elements related to patient data, cancer diagnosis, and outcomes, and mapped them to openEHR archetypes to optimize data processing. To classify cancer diagnosis according to the predefined 17 tumor subgroups, the International Classification of Childhood Cancer, Third Edition (ICCC-3) was used. In phase 2, we defined a data processing plan to extract these data elements from Electronic Health Records (EHR) and additional existing data sources. In phase 3, we designed a reporting dashboard to visualize results for healthcare professionals. <h3>Future perspectives and considerations</h3> Local plans include further automation of data processing, unlocking missing data sources, and adding treatment data. Having a dedicated team and using openEHR with other data (coding) standards facilitates the process and future benchmarking opportunities. <h3>Conclusion</h3> Developing a structured approach for data collection and visualization of the International Childhood Cancer Core Outcomes is an extensive process involving multiple steps. We describe our strategy to facilitate the monitoring of improvements in quality of care in childhood cancer centers and allow future benchmarking of the quality of care.

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Publication Details

Journal
EJC Paediatric Oncology
Published
2025-05-09
DOI
https://doi.org/10.1016/j.ejcped.2025.100239
Primary Topic
Childhood Cancer Survivors' Quality of Life
Type
article
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article

A structured approach for data collection and visualization of the International Childhood Cancer Core Outcomes

Renée L. Mulder, Jaap G. den Hartogh, Miranda P. Dierselhuis, Max M. van Noesel et al.
EJC Paediatric Oncology
Childhood Cancer Survivors' Quality of Life
article

A structured approach for data collection and visualization of the International Childhood Cancer Core Outcomes

Renée L. Mulder, Jaap G. den Hartogh, Miranda P. Dierselhuis, Max M. van Noesel, Melissa Vincent, Hans Merks, Annelies M. C. Mavinkurve‐Groothuis, Bianca F. Goemans, Katja M. J. Heitink‐Pollé, H. Josef Vormoor, Harm van Tinteren, Jop C. Teepen, Marita Partanen, Marry M. van den Heuvel‐Eibrink, Dannis G. van Vuurden, Lisethe Meijer, Martha A. Grootenhuis, Marc H. W. A. Wijnen, Rebecca J. van Kalsbeek, Eelco W. Hoving, Caroline A. Lindemans, Sabine Plasschaert, Hanneke M. van Santen, Ellen Kilsdonk, R.J. Riezebos, Femke K. Aarsen, Elizabeth A. M. Feijen, Leontien C.M. Kremer, N. Franke, Martine van Grotel, Antoinette Y. Schouten-Meeteren, D.W.G.D. Oomen, Wouter J.W. Kollen, Margriet van der Heiden‐van der Loo, József Zsíros, Raphaële R. L. van Litsenburg, Cor van den Bos, Friederike A. G. Meyer‐Wentrup, Melissa M. Hudson, Válerie de Haas, Rob Pieters, Mathew J. Ehrhardt, M.J.R.J. Bouts, L.H. Grundeken
article en

Abstract

<h2>Abstract</h2><h3>Background</h3> Insight into clinically relevant outcomes for children with cancer is crucial for improving treatment and follow-up strategies. The International Childhood Cancer Core Outcome Project developed a harmonized core outcome set, involving patients and providers across all types of childhood cancer. <h3>Objective</h3> This paper highlights the strategy used at the Princess Máxima Center for pediatric oncology for the collection and visualization of the International Childhood Cancer Core Outcomes. <h3>Project phases</h3> In phase 1, we created an overview of data elements related to patient data, cancer diagnosis, and outcomes, and mapped them to openEHR archetypes to optimize data processing. To classify cancer diagnosis according to the predefined 17 tumor subgroups, the International Classification of Childhood Cancer, Third Edition (ICCC-3) was used. In phase 2, we defined a data processing plan to extract these data elements from Electronic Health Records (EHR) and additional existing data sources. In phase 3, we designed a reporting dashboard to visualize results for healthcare professionals. <h3>Future perspectives and considerations</h3> Local plans include further automation of data processing, unlocking missing data sources, and adding treatment data. Having a dedicated team and using openEHR with other data (coding) standards facilitates the process and future benchmarking opportunities. <h3>Conclusion</h3> Developing a structured approach for data collection and visualization of the International Childhood Cancer Core Outcomes is an extensive process involving multiple steps. We describe our strategy to facilitate the monitoring of improvements in quality of care in childhood cancer centers and allow future benchmarking of the quality of care.

EJC Paediatric OncologyVol. 5
St. Jude Children's Research Hospital (US), Stichting Kinderoncologie Nederland (NL), Princess Máxima Center (NL), CURE Childhood Cancer (US)
Openalex Percentile: Top 86%
Childhood Cancer Survivors' Quality of Life
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