Tumor lysis syndrome induced by tebentafusp

Author:

Ruf Theresa1,Leonhardt Anna1,Anz David2,Kunz Wolfgang G3,Röhrle Natascha2,Foerster Paul4,Tomsitz Dirk1,French Lars Einar15ORCID,Seegräber Marlene1,Heinzerling Lucie1ORCID

Affiliation:

1. Department of Dermatology & Allergy, University Hospital, LMU Munich, Munich, 80337, Germany

2. Department of Internal Medicine, University Hospital, LMU Munich, Munich, 80336, Germany

3. Department of Radiology, University Hospital, LMU Munich, Munich, 80336, Germany

4. Department of Ophthalmology, University Hospital, LMU Munich, Munich, 80336, Germany

5. Dr. Philip Frost Department of Dermatology & Cutaneous Surgery, University of Miami Miller School of Medicine, Miami, FL 33125, USA

Abstract

Tebentafusp, a bispecific T-cell receptor fusion protein directed against gp100 and CD3, can improve survival in patients with metastatic uveal melanoma and was recently approved for the treatment of HLA-A*02:01-positive uveal melanoma patients. Since tebentafusp often induces cytokine-release syndrome, doses must be escalated and patients monitored as inpatients after the first infusions. The occurrence of tumor lysis syndrome, a potentially life-threatening condition, after administration of a single dose of tebentafusp, is reported here. With adequate therapy, including the application of rasburicase, the patient made a full recovery. It is important to raise awareness of the adverse event profile of this new therapeutic approach among healthcare professionals to promptly recognize and treat side effects.

Publisher

Future Medicine Ltd

Subject

Oncology,Immunology,Immunology and Allergy

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