Evidence map›Paper›PMID 40419286›Full record

Trial reportBritish journal of haematology2026

Comparability of external and internal control patients for the prospective randomized HOVON-103 trial in older AML patients.

Sjoerd J F Hermans, Jurjen Versluis, Erik D van Werkhoven, Yvette van Norden, Jeroen J W M Janssen, Gerwin A Huls, Thomas Pabst, Dimitri A Breems, Elizabeth Berkx, Avinash G Dinmohamed and 15 more

Abstract readRandomized Controlled TrialComparative StudyMulticenter Study
In one paragraph

Trial report in British journal of haematology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Trial
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

25 authors.

Sjoerd J F HermansErasmus University Medical Center Cancer Institute, Rotterdam, The Netherlands.ORCID https://orcid.org/0000-0002-3906-4584
Jurjen VersluisErasmus University Medical Center Cancer Institute, Rotterdam, The Netherlands.
Erik D van WerkhovenErasmus University Medical Center Cancer Institute, Rotterdam, The Netherlands.
Yvette van NordenErasmus University Medical Center Cancer Institute, Rotterdam, The Netherlands.
Jeroen J W M JanssenDepartment of Haematology, University Medical Centre Nijmegen, Nijmegen, The Netherlands.
Gerwin A HulsDepartment of Hematology, University Medical Center Groningen (UMCG), Groningen, The Netherlands.
Thomas PabstDepartment of Medical Oncology, Inselspital, Bern University Hospital, Bern, Switzerland.ORCID https://orcid.org/0000-0002-6055-5257
Dimitri A BreemsZiekenhuis Netwerk Antwerpen, Antwerp, Belgium.
Elizabeth BerkxDepartment of Research and Development, Netherlands Comprehensive Cancer Organization (IKNL), Utrecht, The Netherlands.
Avinash G DinmohamedDepartment of Research and Development, Netherlands Comprehensive Cancer Organization (IKNL), Utrecht, The Netherlands.ORCID https://orcid.org/0000-0002-4767-6716
Peter C HuijgensDepartment of Research and Development, Netherlands Comprehensive Cancer Organization (IKNL), Utrecht, The Netherlands.
Eric SträngDepartment of Hematology, Oncology, Tumor Immunology, Charité University Medicine, Berlin, Germany.
Jesús María Hernández RivasServicio de Hematología, Hospital Universitario de Salamanca, Universidad de Salamanca, Salamanca, Spain.
Marta SobasDepartment of Hematology, Blood Neoplasms, and Bone Marrow Transplantation, Wroclaw Medical University, Wroclaw, Poland.ORCID https://orcid.org/0000-0003-0781-8668
Rosa Ayala DiazHematology Department, Hospital 12 de Octubre (i+12), Centro Nacional de Investigaciones Oncológicas (CNIO), Complutense University, Madrid, Spain.ORCID https://orcid.org/0000-0002-2699-8353
Joaquin Martinez LopezHematology Department, Hospital 12 de Octubre (i+12), Centro Nacional de Investigaciones Oncológicas (CNIO), Complutense University, Madrid, Spain.ORCID https://orcid.org/0000-0001-5904-0902
Klaus H MetzelerDepartment of Hematology, Cellular Therapy, Hemostaseology and Infectious Diseases, University Medical Center Leipzig, Leipzig, Germany.ORCID https://orcid.org/0000-0003-3920-7490
Torsten HaferlachMLL Munich Leukemia Laboratory, Munich, Germany.
Christian ThiedeDepartment of Medicine I, University Hospital Carl Gustav Carus, Dresden, Germany.ORCID https://orcid.org/0000-0003-1241-2048
Carin A Uyl-de GrootErasmus School of Health Policy & Management, Erasmus University Rotterdam, Rotterdam, The Netherlands.
Lars BullingerDepartment of Hematology, Oncology, and Cancer Immunology, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Bob LöwenbergErasmus University Medical Center Cancer Institute, Rotterdam, The Netherlands.
Gert J OssenkoppeleDepartment of Hematology, Cancer Center Amsterdam, Amsterdam University Medical Centers, Vrije Universiteit University Medical Center, Amsterdam, The Netherlands.
Francesco PignattiOncology and Hematology Office, European Medicines Agency, Amsterdam, The Netherlands.
Jan J CornelissenErasmus University Medical Center Cancer Institute, Rotterdam, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsLeukemia, Myeloid, AcuteAgedAged, 80 and overFemaleHumansMaleProspective StudiesRegistriesacute myeloid leukaemiaclinical trialsexternal control armexternal controlsnon‐randomized studiesreal‐world data

Identifiers

PMID40419286
PMCPMC12819094

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.