TY - JOUR
T1 - Comparability of external and internal control patients for the prospective randomized HOVON-103 trial in older AML patients
AU - Hermans, Sjoerd J.F.
AU - Versluis, Jurjen
AU - van Werkhoven, Erik D.
AU - van Norden, Yvette
AU - Janssen, Jeroen J.W.M.
AU - Huls, Gerwin A.
AU - Pabst, Thomas
AU - Breems, Dimitri A.
AU - Berkx, Elizabeth
AU - Dinmohamed, Avinash G.
AU - Huijgens, Peter C.
AU - Sträng, Eric
AU - Hernández Rivas, Jesús María
AU - Sobas, Marta
AU - Ayala Diaz, Rosa
AU - Martinez Lopez, Joaquin
AU - Metzeler, Klaus H.
AU - Haferlach, Torsten
AU - Thiede, Christian
AU - Uyl-de Groot, Carin A.
AU - Bullinger, Lars
AU - Löwenberg, Bob
AU - Ossenkoppele, Gert J.
AU - Pignatti, Francesco
AU - Cornelissen, Jan J.
N1 - Publisher Copyright:
© 2025 The Author(s). British Journal of Haematology published by British Society for Haematology and John Wiley & Sons Ltd.
PY - 2025/5/26
Y1 - 2025/5/26
N2 - Real-world data (RWD) previously contributed to post-marketing regulatory decision-making, but are currently also considered as external controls to single-arm trials. The use of RWD control data may be compromised by methodological issues, urging validation of RWD control cohorts. Two external control cohorts of newly diagnosed acute myeloid leukaemia patients, one registered by the HARMONY Alliance (HA) and one by the Netherlands Cancer Registry (NCR), were compared to the control arm of the randomized HOVON-103 trial (H103 controls). All patients, aged >65 years with a WHO performance score of 0–2 (or missing), received standard induction chemotherapy. 1:1 propensity score calliper matching (PSM) was applied to improve comparability, and overall (OS) and relapse-free survival (RFS) were assessed. Fewer data elements were available in external cohorts compared to H103 controls, specifically in the NCR cohort. Baseline characteristics of the external cohorts differed from H103 controls; missing data were also more frequent and predominantly concerned WHO performance score. After PSM, HA patients demonstrated non-significantly different OS and RFS to H103 controls at 2 years (26 ± 4% vs. 31 ± 5%, p = 0.59; 24 ± 5% vs. 30 ± 6%, p = 0.52), while NCR patients had 12% lower OS (28 ± 4% vs. 40 ± 4%, p = 0.21). Validation of external control cohorts is needed before incorporating RWD control data into comparative analyses, as missing data, specifically comorbidities, and residual confounding may limit comparability.
AB - Real-world data (RWD) previously contributed to post-marketing regulatory decision-making, but are currently also considered as external controls to single-arm trials. The use of RWD control data may be compromised by methodological issues, urging validation of RWD control cohorts. Two external control cohorts of newly diagnosed acute myeloid leukaemia patients, one registered by the HARMONY Alliance (HA) and one by the Netherlands Cancer Registry (NCR), were compared to the control arm of the randomized HOVON-103 trial (H103 controls). All patients, aged >65 years with a WHO performance score of 0–2 (or missing), received standard induction chemotherapy. 1:1 propensity score calliper matching (PSM) was applied to improve comparability, and overall (OS) and relapse-free survival (RFS) were assessed. Fewer data elements were available in external cohorts compared to H103 controls, specifically in the NCR cohort. Baseline characteristics of the external cohorts differed from H103 controls; missing data were also more frequent and predominantly concerned WHO performance score. After PSM, HA patients demonstrated non-significantly different OS and RFS to H103 controls at 2 years (26 ± 4% vs. 31 ± 5%, p = 0.59; 24 ± 5% vs. 30 ± 6%, p = 0.52), while NCR patients had 12% lower OS (28 ± 4% vs. 40 ± 4%, p = 0.21). Validation of external control cohorts is needed before incorporating RWD control data into comparative analyses, as missing data, specifically comorbidities, and residual confounding may limit comparability.
UR - http://www.scopus.com/inward/record.url?scp=105006711845&partnerID=8YFLogxK
U2 - 10.1111/bjh.20185
DO - 10.1111/bjh.20185
M3 - Article
C2 - 40419286
AN - SCOPUS:105006711845
SN - 0007-1048
JO - British Journal of Haematology
JF - British Journal of Haematology
M1 - bjh.20185
ER -