# Refractory Epstein-Barr Virus-Negative Diffuse Large B-Cell Lymphoma Post-Transplant Lymphoproliferative Disorder in a Renal Transplant Patient Treated With Bispecific Antibody Therapy

**Authors:** Austin Frisch, Bobby Se, Eric Martin, Haresh Mani, Stephen Medlin, Zartash Gul

PMC · DOI: 10.14740/jmc5186 · Journal of Medical Cases · 2025-10-10

## TL;DR

A renal transplant patient with refractory EBV-negative lymphoma was treated with bispecific antibody therapy, but the outcome was poor, highlighting the need for better treatment options.

## Contribution

This case study explores bispecific antibody therapy as a potential novel treatment for refractory EBV-negative PTLD.

## Key findings

- Bispecific antibody therapy was used as a fourth-line treatment for refractory EBV-negative PTLD.
- The patient experienced multiple hospitalizations and eventually opted for hospice care.
- The case highlights the limited success of current therapies and the need for novel treatment strategies.

## Abstract

Post-transplant lymphoproliferative disorder (PTLD) is a rare disorder that can occur in both stem cell and organ transplant recipients. Most cases of PTLD arise from Epstein-Barr virus (EBV)-induced oncogenesis but it can be EBV-negative. The treatment algorithm involves reduction in immunosuppression combined with anti-CD20 antibody treatment followed by chemotherapy. Despite this, mortality is still high, and many patients have refractory disease. Refractory PTLD is challenging to treat, and the data on treatment are limited. Both stem cell transplant and chimeric antigen receptor T-cell (CAR-T) therapies have been described in case reports and small reviews, but success has been limited. Hence, there is a need for novel therapies and clinical trials to formulate better treatment plans. Here, we present a complex case of refractory EBV-negative PTLD that progressed on third-line treatment. Given the patient’s limited options, glofitamab, a bispecific antibody therapy, was initiated in attempt to bridge to CAR-T therapy. Unfortunately, the patient encountered multiple hospitalizations and eventually elected for hospice care not long after initiation of this fourth-line regimen began. Herein, we detail the diagnosis and treatment options for EBV-negative refractory PTLD with an in-depth literature review that highlights bispecific antibodies as a potential novel therapy.

## Linked entities

- **Diseases:** Post-Transplant Lymphoproliferative Disorder (MONDO:0019088)

## Full-text entities

- **Genes:** KRT20 (keratin 20) [NCBI Gene 54474] {aka CD20, CK-20, CK20, K20, KRT21}
- **Diseases:** PTLD (MESH:D008232), Large B-Cell Lymphoma Post-Transplant Lymphoproliferative Disorder (MESH:D016393)
- **Chemicals:** glofitamab (MESH:C000720108), CAR-T (-)
- **Species:** Homo sapiens (human, species) [taxon 9606], human gammaherpesvirus 4 (Epstein Barr virus, no rank) [taxon 10376]

## Full text

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## Figures

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## References

23 references — full list in the complete paper: https://tomesphere.com/paper/PMC12758035/full.md

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Source: https://tomesphere.com/paper/PMC12758035