Underweight <scp>BMI</scp> Independently Predicts Inferior Survival in <scp>DLBCL</scp> Treated With R‐ <scp>CHOP</scp> : A Lymphoma Registry Study

OBJECTIVES: BMI may capture clinically relevant differences in host reserve and treatment vulnerability in diffuse large B-cell lymphoma (DLBCL). We evaluated the association between BMI and survival outcomes. METHODS: Adults with DLBCL receiving first-line R-CHOP chemoimmunotherapy from 2016 to 2026 were identified from the Lymphoma and Related Diseases Registry. BMI was analysed as underweight, normal weight/overweight, obese Class I and obese Class II/III. Overall survival (OS) and progression-free survival (PFS) were analysed using Kaplan-Meier and Cox models adjusted for International Prognostic Index (IPI) components, sex and cardiac history. RESULTS: Among 1600 patients, 43 (2.7%) were underweight, 303 (18.9%) had obese Class I BMI and 198 (12.4%) had obese Class II/III BMI. At median follow-up of 35.4 months, 342 deaths occurred, including 15 in underweight patients. OS differed by BMI category (log-rank p = 0.017), whereas PFS did not (log-rank p = 0.082). In complete-case multivariable analysis, underweight BMI remained associated with inferior OS (adjusted HR, 1.89; 95% CI, 1.06-3.37). Exploratory analyses did not identify chemotherapy exposure, including upfront dose reduction, or measured malnutrition/systemic illness markers that explained this association. CONCLUSIONS: Underweight BMI identified patients at increased risk of inferior survival, even after adjustment for IPI-based prognostic factors. Obese BMI categories were not associated with inferior survival.

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Journal
European Journal Of Haematology
Published
2026-08-18
DOI
https://doi.org/10.1111/ejh.70295
Primary Topic
Cancer Risks and Factors
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article

Underweight BMI Independently Predicts Inferior Survival in DLBCL Treated With R‐ CHOP : A Lymphoma Registry Study

Eliza A. Hawkes, Eliza Chung, Tasman Armytage, Denise Lee et al.
European Journal Of Haematology
Cancer Risks and Factors
article

Underweight BMI Independently Predicts Inferior Survival in DLBCL Treated With R‐ CHOP : A Lymphoma Registry Study

Eliza A. Hawkes, Eliza Chung, Tasman Armytage, Denise Lee, Erica M. Wood, Chan Yoon Cheah, Geoffrey Chong, Cameron Wellard, Yao Yao, Anna Johnston, Susan Morgan, Serif Sungur, Nada Hamad
article en

Abstract

OBJECTIVES: BMI may capture clinically relevant differences in host reserve and treatment vulnerability in diffuse large B-cell lymphoma (DLBCL). We evaluated the association between BMI and survival outcomes. METHODS: Adults with DLBCL receiving first-line R-CHOP chemoimmunotherapy from 2016 to 2026 were identified from the Lymphoma and Related Diseases Registry. BMI was analysed as underweight, normal weight/overweight, obese Class I and obese Class II/III. Overall survival (OS) and progression-free survival (PFS) were analysed using Kaplan-Meier and Cox models adjusted for International Prognostic Index (IPI) components, sex and cardiac history. RESULTS: Among 1600 patients, 43 (2.7%) were underweight, 303 (18.9%) had obese Class I BMI and 198 (12.4%) had obese Class II/III BMI. At median follow-up of 35.4 months, 342 deaths occurred, including 15 in underweight patients. OS differed by BMI category (log-rank p = 0.017), whereas PFS did not (log-rank p = 0.082). In complete-case multivariable analysis, underweight BMI remained associated with inferior OS (adjusted HR, 1.89; 95% CI, 1.06-3.37). Exploratory analyses did not identify chemotherapy exposure, including upfront dose reduction, or measured malnutrition/systemic illness markers that explained this association. CONCLUSIONS: Underweight BMI identified patients at increased risk of inferior survival, even after adjustment for IPI-based prognostic factors. Obese BMI categories were not associated with inferior survival.

European Journal Of Haematology
University of Tasmania (AU), The University of Western Australia (AU), Launceston General Hospital (AU), Austin Hospital (AU), Gosford Hospital (AU), Sir Charles Gairdner Hospital (AU), Royal Hobart Hospital (AU), St Vincent's Hospital Sydney (AU), Eastern Health (AU), Ballarat Health Services (AU), Calvary Mater Newcastle Hospital (AU), Olivia Newton-John Cancer Wellness & Research Centre (AU), Alfred Health (AU), Austin Health (AU), Olivia Newton-John Cancer Research Institute (AU), Monash University (AU)
Zero hunger
Openalex Percentile: Top 12%
Cancer Risks and Factors
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