# Antibiotic Use Before CAR-T Treatment Is Associated with Inferior Outcomes in DLBCL Lymphoma Patients

**Authors:** Anja Bullegas, Inna Shaforostova, Katja Seipel, Marie-Noëlle Kronig, Henning Nilius, Ulrike Bacher, Thomas Pabst

PMC · DOI: 10.3390/biomedicines14020298 · Biomedicines · 2026-01-29

## TL;DR

Using antibiotics before CAR-T treatment in lymphoma patients is linked to worse survival outcomes, possibly due to changes in gut bacteria.

## Contribution

This study identifies antibiotic use before CAR-T therapy as a potential factor affecting treatment outcomes in DLBCL patients.

## Key findings

- Patients who used antibiotics before CAR-T had significantly worse progression-free and overall survival.
- Multiple antibiotic courses and shorter intervals before CAR-T were associated with poorer outcomes.
- The study suggests antibiotic-induced gut microbiome changes may impact CAR-T efficacy.

## Abstract

Background/Objectives: CAR-T-cell therapy has become a key treatment for relapsed or refractory hematologic malignancies such as diffuse large B-cell lymphoma (r/r DLBCL), although patient outcomes differ considerably. The intestinal microbiome has been proposed as an important factor influencing CAR-T-cell therapy efficacy; accordingly, antibiotic exposure, which may induce dysbiosis, has been associated with inferior outcomes after CAR-T-cell therapy. Methods: We retrospectively analyzed clinical data from 140 patients to assess the impact of infection-related antibiotic therapy prior to CAR-T-cell therapy, stratifying them into two cohorts: 67 patients with previous antibiotic exposure and 73 without exposure. Results: Patients exposed to antibiotics prior to CAR-T therapy had significantly reduced progression-free survival (p = 0.016) and overall survival (p = 0.002) compared to those without exposure. Multiple antibiotic courses and shorter intervals between the last antibiotic treatment and CAR-T-cell therapy were linked to poorer outcomes. Conclusions: Our data suggest that pre-CAR-T-cell-therapy antibiotic exposure is associated with inferior outcomes, although it remains unclear whether this effect is causal or reflects underlying patient comorbidities. These findings highlight the need for further studies investigating the role of antibiotic-induced dysbiosis on CAR-T-cell therapy efficacy.

## Linked entities

- **Diseases:** diffuse large B-cell lymphoma (MONDO:0018905), DLBCL (MONDO:0018905)

## Full-text entities

- **Genes:** CD19 (CD19 molecule) [NCBI Gene 930] {aka B4, CVID3}, CXADRP1 (CXADR pseudogene 1) [NCBI Gene 653108] {aka CAR, CXADRP}
- **Diseases:** irritable bowel disease (MESH:D043183), CRS (MESH:D000080424), DLBCL Lymphoma (MESH:D008223), hypogammaglobulinemia (MESH:D000361), infarctions (MESH:D007238), cardiac arrhythmias (MESH:D001145), B-cell lymphoma (MESH:D016393), heart failure (MESH:D006333), myocardial (MESH:D009202), DLBCL (MESH:D016403), hematologic malignancies (MESH:D019337), infectious (MESH:D003141), chronic infections (MESH:D000088562), injury to (MESH:D014947), inflammation (MESH:D007249), thrombosis (MESH:D013927), Helicobacter pylori (MESH:D016481), hematological diseases (MESH:D006402), hypertension (MESH:D006973), Deaths (MESH:D003643), PD (MESH:D010300), coronary heart disease (MESH:D003327), ICANS (MESH:C000722498), Cardiovascular diseases (MESH:D002318), neurotoxicity (MESH:D020258), infection (MESH:D007239), dysbiosis (MESH:D064806), Gastrointestinal diseases (MESH:D005767), tumor (MESH:D009369), toxicities (MESH:D064420)
- **Chemicals:** fluconazole (MESH:D015725), steroids (MESH:D013256), valaciclovir (MESH:D000077483), cefepime (MESH:D000077723), meropenem (MESH:D000077731), acetate (MESH:D000085), SCFAs (MESH:D005232), pentanoate (MESH:D014631), Lisocabtagene maraleucel (-), T (MESH:D014316), Tocilizumab (MESH:C502936), piperacillin-tazobactam (MESH:D000077725)
- **Species:** gut metagenome (species) [taxon 749906], Clostridia (class) [taxon 186801], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12937898/full.md

## References

23 references — full list in the complete paper: https://tomesphere.com/paper/PMC12937898/full.md

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Source: https://tomesphere.com/paper/PMC12937898