Effect of pre-biopsy steroids on diagnostic yield in diffuse large B-cell lymphoma (DLBCL).

S Sathwik Madireddy (1Brown University, Providence, United States) K Kelly Pan (1Brown University, Department of Internal Medicine, Providence, United States) S Sovijja Pou (Brown University Health, Providence, RI) K Kaavya Mandi (Brown University Health, Providence, RI) H Huang Ding (Brown University Health, Providence, RI) A Alex Friefeld (Brown University Health, Providence, RI) C Christina Raker (Brown University Health, Providence, RI) R Ross Terada (10Alpert Medical School of Brown University, Department of Medicine, Providence, United States) C Charles J. Milrod (Brown University Health, Providence, RI) A Ari Pelcovits (1Brown University, Providence, United States)

Abstract

7072 Background: DLBCL is an aggressive lymphoma, and patients (pts) often require urgent steroid administration for symptom relief or organ compromise prevention. Steroids before biopsy are avoided due to concerns about diagnostic accuracy. This supposition remains underexplored, with limited evidence supporting this practice. Methods: A retrospective chart review of pts with a diagnosis of DLBCL at Brown University Health between 2015 and 2024 was conducted for baseline demographics, steroid administration within 30 days of first biopsy, type and dose of steroids, markers of disease severity, type of biopsy, and biopsy results. Exclusion criteria included relapsed/refractory DLBCL. Statistical analysis was conducted using Chi-square test, T-test, and logistic regression. Results: 365 pts met inclusion criteria, of whom 65 received steroids prior to their first biopsy. Both steroid-treated and steroid-naive pts had similar baseline demographics (age) and markers of disease severity (LDH, “Double HIT” status, IPI score, and Stage), (p > 0.05). Both groups had similar rates of diagnostic first biopsies (p > 0.05). After initial negative biopsies, similar rates of diagnostic repeat biopsies were observed. Neither group had a significant difference in treatment delay from initial negative biopsy to start of chemotherapy (p > 0.05). Logistic regression analysis showed no statistical significance in the relationship between total dose of steroids and the likelihood of a diagnostic biopsy result (p = 0.07). Type of biopsy influenced diagnostic yield: fine needle aspiration (n = 32) was inferior with 28% diagnostic biopsies compared with core needle, excisional or incisional biopsies (n = 284) at 88% (p < 0.001). Conclusions: No significant differences were observed in biopsy success rates or treatment delays between steroid-treated and steroid-naive patients. These results support the safe use of corticosteroids when clinically indicated. Notably, biopsy type, rather than steroid exposure, was the primary determinant of diagnostic success, with fine needle aspiration yielding significantly lower diagnostic rates. These findings reinforce the importance of biopsy selection and support corticosteroid use without compromising diagnostic accuracy. Characteristics Steroids-treated (n=65) Steroid-naive (n=283) P value Age (years), mean (95% CI) 67 (64 - 70) 67 (65 - 69) 0.805 Advanced Stage, proportion (95% CI) 64.15% 71.48% 0.286 LDH (U/L), mean (95% CI) 392 (297 - 487) 364 (315 - 413) 0.637 Percent “Double Hit” 13.85% 9.54% 0.304 Percent first biopsy diagnostic 86.67% 81.79% 0.219 Percent repeat biopsy diagnostic 87.50% 97.92% 0.116 Days from first negative biopsy to treatment, mean (95% CI) 39.5 (12.6 - 66.4) 50.7 (42.9 - 58.5) 0.327 Total steroid dose in prednisone equivalents (mg), mean (95% CI) 261 (193 - 329) 0 N/A Total days on steroids, mean (95% CI) 6.8 (4.5 - 9.1) 0 N/A

Article Details

Volume / Issue Vol. 43, Issue 16_suppl
Published June 01, 2025
Pages 7072-7072
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (10)

S

Sathwik Madireddy

1Brown University, Providence, United States

K

Kelly Pan

1Brown University, Department of Internal Medicine, Providence, United States

S

Sovijja Pou

Brown University Health, Providence, RI

K

Kaavya Mandi

Brown University Health, Providence, RI

H

Huang Ding

Brown University Health, Providence, RI

A

Alex Friefeld

Brown University Health, Providence, RI

C

Christina Raker

Brown University Health, Providence, RI

R

Ross Terada

10Alpert Medical School of Brown University, Department of Medicine, Providence, United States

C

Charles J. Milrod

Brown University Health, Providence, RI

A

Ari Pelcovits

1Brown University, Providence, United States