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Dessau‐Arp, Andriette

Mayo Clinic

Hospital South West Jutland

Citations 2

Impact of Trial Eligibility Criteria on Outcomes of 1183 Patients With Follicular Lymphoma Treated in the Real‐World Setting
Bennedsen, Tine Litske , Simonsen, Mikkel Runason , Jensen, Paw , Josefsson, Pär, Khurana, Arushi , Clausen, Michael Roost , Dessau‐Arp, Andriette, Jørgensen, Jennifer Bøgh , Jørgensen, Judit , Larsen, Thomas Stauffer , Pedersen, Lars Møller , Jakobsen, Lasse Hjort , Joergensen, Judit Mészáros , Clausen, Michael Roost , Pedersen, Lars Møller , Jensen, Paw , Brown, Peter de Nully , Maurer, Matthew J. , El‐Galaly, Tarec Christoffer

European Journal of Haematology | January 9, 2025 | Volume: 114 | Issue: 5 | Pages: 832-839

10.1111/ejh.14373 Get It

ABSTRACTThe development of new first‐line treatments for patients with follicular lymphoma (FL) is becoming increasingly challenging due to already excellent survival outcomes. The present study investigated the outcomes of patients with FL who underwent contemporary first‐line therapies but would not have been eligible for inclusion in recent trials and explored how commonly used in/exclusion criteria impacted their survival outcomes. This study included adult patients diagnosed with FL in the period 2000–2018 registered in the Danish Lymphoma Registry. Through searches on ClinicalTrials.gov, four recent 1st line phase 3 randomized controlled trials with R‐Bendamustine, R‐CVP, and/or R‐CHOP as control or experimental arms were included. Inclusion and exclusion criteria for each trial were retrieved and categorized. Patients were then divided into trial‐eligible and ineligible groups according to blood test results correlated to organ function and ECOG performance score (PS). Survival outcomes were significantly worse among trial‐ineligible patients, with adjusted differences between trial‐eligible and ineligible patients of 12%–20% in five‐year overall survival (OS) overall. Inclusion criteria based on PS and renal function were the main drivers of OS differences. More inclusive trials will lead to faster recruitment and secure focus on developing medicines for the group of patients with the worst outcomes.