Age, Comorbidity Burden and Treatment Outcomes in Mature B-Cell Lymphoproliferative Disorders: A Real-World Study.
4 affiliations
- 1Faculty of Science and Medicine, University of Fribourg, Fribourg, Switzerland.
- 2CHUV Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.
- 3HFR Hôpital Fribourgeois, Villars-sur-Glâne, Switzerland.
- 4Department of Medical Oncology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Abstract
Introduction
Treatment decisions in older patients with mature B-cell lymphoproliferative disorders (MBLD) are frequently guided by chronological age and comorbidity burden, although their ability to predict clinically relevant outcomes remains uncertain.Methods
We conducted a retrospective real-world study including 172 patients with MBLD between 2016 and 2021, assessing the association of age and comorbidity burden (standardised using the Cumulative Illness Rating Scale for Geriatrics, CIRS-G score) with treatment intensity, toxicity, and clinical outcomes.Results
Treatment intensity decreased significantly with both age (p = 0.003) and CIRS-G score (p < 0.001). However, neither age nor CIRS-G score was associated with an increased rate of treatment-related toxic events. In contrast, older age was associated with worse overall survival and lower response rates (all p < 0.05), whereas CIRS-G score was not significantly associated with these outcomes. Similar associations between age and outcomes were observed in the DLBCL subgroup.Conclusion
In this real-world cohort of patients with MBLD, chronological age was more consistently associated with treatment patterns and clinical outcomes than comorbidity burden as measured by the CIRS-G score. These findings suggest that chronological age alone may not adequately capture the heterogeneity of older patients and support the use of more comprehensive assessments of frailty and functional status to inform treatment decisions.
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BibTeX
@article{nasrinfar2026comorbidity,
title = {{Age, Comorbidity Burden and Treatment Outcomes in Mature B-Cell Lymphoproliferative Disorders: A Real-World Study.}},
author = {Kevin Nasrinfar and Harrison Wildhaber and Rudolf Rohr and Gaëlle Rhyner Agocs and Urban Novak and Alessandra Curioni-Fontecedro and Vérène Dougoud-Chauvin},
journal = {Cancer medicine},
year = {2026},
month = nov,
doi = {10.1002/cam4.72460},
url = {https://europepmc.org/article/MED/42968459},
note = {CC BY-NC-ND},
}
RIS
TY - JOUR
TI - Age, Comorbidity Burden and Treatment Outcomes in Mature B-Cell Lymphoproliferative Disorders: A Real-World Study.
AU - Kevin Nasrinfar
AU - Harrison Wildhaber
AU - Rudolf Rohr
AU - Gaëlle Rhyner Agocs
AU - Urban Novak
AU - Alessandra Curioni-Fontecedro
AU - Vérène Dougoud-Chauvin
PY - 2026
DA - 2026/11/01
JO - Cancer medicine
DO - 10.1002/cam4.72460
UR - https://europepmc.org/article/MED/42968459
AB - Introduction Treatment decisions in older patients with mature B-cell lymphoproliferative disorders (MBLD) are frequently guided by chronological age and comorbidity burden, although their ability to predict clinically relevant outcomes remains uncertain.Methods We conducted a retrospective real-world study including 172 patients with MBLD between 2016 and 2021, assessing the association of age and comorbidity burden (standardised using the Cumulative Illness Rating Scale for Geriatrics, CIRS-G score) with treatment intensity, toxicity, and clinical outcomes.Results Treatment intensity decreased significantly with both age (p = 0.003) and CIRS-G score (p < 0.001). However, neither age nor CIRS-G score was associated with an increased rate of treatment-related toxic events. In contrast, older age was associated with worse overall survival and lower response rates (all p < 0.05), whereas CIRS-G score was not significantly associated with these outcomes. Similar associations between age and outcomes were observed in the DLBCL subgroup.Conclusion In this real-world cohort of patients with MBLD, chronological age was more consistently associated with treatment patterns and clinical outcomes than comorbidity burden as measured by the CIRS-G score. These findings suggest that chronological age alone may not adequately capture the heterogeneity of older patients and support the use of more comprehensive assessments of frailty and functional status to inform treatment decisions.
SN - 2045-7634
ER -