Extracting Systemic Anticancer Treatment Lines from the Danish National Patient Registry for Solid Tumour Patients Treated in the North Denmark Region Between 2009 and 2019

被引:0
作者
Vesteghem, Charles [1 ,2 ,3 ,6 ,7 ]
Bogsted, Martin [1 ,2 ,3 ]
Cronin-Fenton, Deirdre [4 ]
Poulsen, Laurids Ostergaard [2 ,3 ,5 ]
机构
[1] Aalborg Univ Hosp, Ctr Clin Data Sci, Aalborg, Denmark
[2] Aalborg Univ Hosp, Aalborg, Denmark
[3] Aalborg Univ Hosp, Clin Canc Res Ctr, Aalborg, Denmark
[4] Aarhus Univ, Dept Clin Epidemiol, Dept Clin Med, Aarhus, Denmark
[5] Aalborg Univ Hosp, Dept Oncol, Aalborg, Denmark
[6] Aalborg Univ, Ctr Clin Data Sci, Selma Lagerlofs Vej 249, DK-9260 Gistrup, Denmark
[7] Aalborg Univ Hosp, Selma Lagerlofs Vej 249, DK-9260 Gistrup, Denmark
关键词
anticancer treatment; epidemiology; patient trajectory; Danish National Patient Register; treatment line; VALIDITY;
D O I
10.2147/CLEP.S442591
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background: Reconstructing patient treatment trajectories is important to generate real-world evidence for epidemiological studies. The Danish National Patient Registry (DNPR) contains information about drug prescriptions and could therefore be used to reconstruct treatment trajectories. We aimed to evaluate and enhance two existing methods to reconstruct systemic anticancer treatment trajectories. Methods: This study was based on data from 8738 consecutive patients with solid tumors treated in the North Denmark Region between 2009 and 2019. Two approaches found in the literature as well as two new approaches were applied to the DNPR data. All methods relied on time intervals between two consecutive drug administrations to determine if they belonged to the same treatment line. MedOnc, a local dataset from the Department of Oncology, Aalborg University Hospital was used as a reference. To evaluate the performance of each method, F1-scores were calculated after matching the lines identified in both datasets. We used three different matching strategies: stringent matching, loose matching, and matching based on line numbers, controlling for overfitting. Results: Overall, the two new approaches outperformed the simpler and best performing of the two existing methods, with F1-scores of 0.47 and 0.45 vs 0.44 for stringent matching and 0.84 and 0.83 vs 0.82 for loose matching. Nevertheless, only one of the new methods outperformed the existing simpler method when matching on the number of lines (0.73 vs 0.72). Large differences were seen by cancer site, especially for the stringent and line number matchings. Performances were relatively stable by calendar year. Conclusion: The high F1-scores for the new methods confirm that they should be generally preferred to reconstruct systemic anticancer treatment trajectories using the DNPR.
引用
收藏
页码:165 / 174
页数:10
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