A Real‐World Data‐Based Analysis of Prognostic Indices as Part of Trial Eligibility Criteria in Diffuse Large B‐Cell Lymphoma Patients

Author:

Jelicic Jelena1ORCID,Juul‐Jensen Karen1,Bukumiric Zoran2,Runason Simonsen Mikkel34,Roost Clausen Michael5ORCID,Ludvigsen Al‐Mashhadi Ahmed36,Schou Pedersen Robert7,Bjørn Poulsen Christian89,Ortved Gang Anne910,Brown Peter910,El‐Galaly Tarec Christoffer13101112,Stauffer Larsen Thomas113

Affiliation:

1. Department of Hematology Odense University Hospital Odense Denmark

2. Institute for Medical Statistics and Informatics University of Belgrade, Faculty of Medicine Belgrade Serbia

3. Department of Hematology, Clinical Cancer Research Center Aalborg University Hospital Aalborg Denmark

4. Department of Mathematical Sciences Aalborg University Aalborg Denmark

5. Department of Hematology Vejle Hospital, Sygehus Lillebaelt Vejle Denmark

6. Department of Hematology Aarhus University Hospital Aarhus Denmark

7. Department of Hematology Regional Hospital Gødstrup Denmark

8. Department of Hematology Zealand University Hospital Roskilde Denmark

9. Department of Clinical Medicine University of Copenhagen Denmark

10. Department of Hematology Copenhagen University Hospital, Rigshospitalet Denmark

11. Clinical Epidemiology Division Karolinska Institutet Stockholm Sweden

12. Department of Medicine Solna Karolinska Institutet Stockholm Sweden

13. Department of Clinical Research University of Southern Denmark Odense Denmark

Abstract

ABSTRACTObjectivesRecent front‐line clinical trials used the International Prognostic Index (IPI) to identify trial‐eligible patients with newly diagnosed diffuse large B‐cell lymphoma (DLBCL). However, many IPI‐like variants with improved accuracy have been developed over the years for rituximab‐treated patients.MethodsWe assessed the impact of International Prognostic Indices on patient enrolment in clinical trials, aiming to exclude low‐risk IPI patients based on POLARIX/EPCORE DLBCL‐2 trial criteria.ResultsWe identified 2877 patients in the Danish Lymphoma Registry who would have been eligible for the POLARIX trial if patients with IPI 0–1 scores were included. IPI and NCCN‐IPI assigned 33.3% and 11.9% of patients to the low‐risk group, respectively. Shorter 5‐year overall survival (91.4% vs. 97.5%), higher relapse rate (9.9% vs. 4.4%), and more deaths (16.1% vs. 4.4%) occurred in the low‐risk IPI group compared with low‐risk NCCN‐IPI group. Analyzed models failed to identify true high‐risk patients with poor prognosis. Similar results were found in the confirmatory cohort developed based on EPCORE DLBCL‐2 trial eligibility criteria.ConclusionTrue low‐risk patients are more optimal identified by NCCN‐IPI and should be excluded from front‐line clinical trials due to their excellent prognosis. However, additional high‐risk factors besides clinical prognostic models need to be considered when selecting trial‐eligible patients.

Publisher

Wiley

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