Abstract
We report a case of bilateral intraocular infiltration of DLBCL after CAR-T therapy. Retrospective case report. A 62-year-old Caucasian male with medical history of high-grade DLBCL presented with papillitis and vitritis upon completion of CAR-T therapy. Thorough infectious and diagnostic work-ups were performed. Diagnostic vitreous tap revealed intraocular lymphoma. The patient received external beam radiotherapy to both orbits with dramatic improvement in disc edema and vitritis. However, subsequent MRI showed development of intracranial metastatic disease, and the patient died within the same month. Atypical intraocular metastasis of DLBCL may occur following CAR-T therapy and may indicate secondary changes in immunosurveillance within immune-privileged sites such as the eye.
Overview
- The study focuses on a case report of a patient with high-grade DLBCL who developed bilateral intraocular infiltration after CAR-T therapy. The hypothesis being tested is whether CAR-T therapy can cause atypical intraocular metastasis of DLBCL. The methodology used for the experiment includes a retrospective case report of the patient's medical history, diagnostic work-ups, and treatment outcomes. The primary objective of the study is to describe the patient's clinical presentation, diagnostic work-up, and treatment outcomes, as well as to discuss the implications of this case for future research and clinical practice.
Comparative Analysis & Findings
- The study compares the patient's clinical presentation and treatment outcomes before and after CAR-T therapy. The patient developed bilateral intraocular infiltration of DLBCL after CAR-T therapy, which was diagnosed through a vitreous tap. The patient received external beam radiotherapy to both orbits, which resulted in improvement in disc edema and vitritis. However, subsequent MRI showed development of intracranial metastatic disease, and the patient died within the same month. The study's findings suggest that atypical intraocular metastasis of DLBCL may occur following CAR-T therapy and may indicate secondary changes in immunosurveillance within immune-privileged sites such as the eye.
Implications and Future Directions
- The study's findings highlight the potential risks and complications associated with CAR-T therapy, particularly in immune-privileged sites such as the eye. The study suggests that further research is needed to better understand the mechanisms underlying atypical intraocular metastasis of DLBCL following CAR-T therapy and to develop strategies to prevent or manage these complications. Possible future research directions include prospective studies to investigate the incidence and risk factors for atypical intraocular metastasis of DLBCL following CAR-T therapy, as well as studies to evaluate the efficacy and safety of different treatment approaches for this complication.