Old Pathogens-New Patient Types: Infections in a CAR T-Cell Recipient. Could It Get Any More Complicated?
Monica Melchio, Joshua A Hill, Maunank Shah, Dionysios Neofytos, Massimiliano Gambella, Anna Maria Raiola, Emanuele Delfino, Elisa Balletto, et al. (11 authors)
Transplant infectious disease : an official journal of the Transplantation Society · 2025-01
Abstract
The case discussed involves a 41-year-old Italian man who was a candidate for chimeric antigen receptor T-cell therapy (CAR-T) for mediastinal diffuse large B-cell lymphoma. His CAR-T treatment was postponed several times due to prolonged relapsing COVID-19 and new onset of pulmonary Mycobacterium tuberculosis diseases. After 11 weeks of antimycobacterial treatment, CAR T-cell therapy was performed, but complicated by cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS). Two months after CAR-T, the patient developed invasive pulmonary aspergillosis due to A. fumigatus. He was successfully treated with a 6-month course of antitubercular therapy and an 8-month course of antifungal therapy with isavuconazole. Lobectomy was performed due to episodes of severe hemoptysis. The challenging issues of diagnosis, choice, and management of treatments, including drug-drug interactions and length of therapy, are discussed.
MeSH terms
- Humans
- Male
- Adult
- Immunotherapy, Adoptive
- COVID-19
- Lymphoma, Large B-Cell, Diffuse
- Cytokine Release Syndrome
- SARS-CoV-2
- Receptors, Chimeric Antigen
- Invasive Pulmonary Aspergillosis
- Antifungal Agents
- Aspergillus fumigatus
- Triazoles
- Tuberculosis, Pulmonary
- Nitriles
- Mediastinal Neoplasms
- Pyridines
- Neurotoxicity Syndromes
- Antitubercular Agents