Nivolumab-induced systemic capillary leak syndrome as an ultra rare life-threatening phenomenon of late toxicity and intravenous immunoglobulin efficacy

Author:

Polishchuk Ilya1,Yakobson Alexander2,Zemel Melanie3,A Sharb Adam4,Shalata Walid2,Rosenberg Eli1,A Kian Tawfeek4,Alguayn Farouq4,Peled Nir2,Rouvinov Keren2,Alguayn Wafeek4,Kian Waleed2

Affiliation:

1. Internal Medicine Ward, Soroka Medical Center & Ben-Gurion University, Beer-Sheva, Israel

2. The Legacy Heritage Oncology Center & Dr Larry Norton Institute, Soroka Medical Center & Ben-Gurion University, Beer-Sheva, Israel

3. Medical School for International Health, Ben-Gurion University of The Negev, Beer-Sheva, Israel

4. Faculty of Health Sciences, Ben-Gurion University of The Negev, Beer-Sheva, Israel

Abstract

Systemic capillary leak syndrome (SCLS) is a life-threatening disease. It is characterized by severe capillary hyperpermeability to proteins resulting in hemoconcentration, hypoalbuminemia and hypovolemic shock. Its treatment remains supportive, and the prognosis is generally poor. We report on a 51-year old male with melanoma treated with nivolumab for 1 year. 1 month following the completion of the treatment, the patient presented with signs of hypovolemic shock, anasarca, hemoconcentration and hypoalbuminemia. After excluding other diseases, a diagnosis of nivolumab-induced systemic capillary leak syndrome was made. A high dose of intravenous steroid therapy was promptly initiated without any significant clinical improvement. Intravenous immunoglobulin therapy was then administered with normalization of blood pressure, hemoconcentration and complete resolution of anasarca. Intravenous immunoglobulin should be considered a first-line treatment option for this rare phenomenon.

Publisher

Future Medicine Ltd

Subject

Oncology,Immunology,Immunology and Allergy

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