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Cytokine release syndrome induced by immune checkpoint inhibitor treatment for uterine cervical cancer recurrence: A case report.

Authors :
Sekimata, Mao
Kinjo, Yasuyuki
Tohyama, Atsushi
Murakami, Midori
Hashiwaki, Sayumi
Saito, Yuma
Higami, Shota
Hagimoto, Marina
Taketomi, Ruka
Hoshino, Kaori
Harada, Hiroshi
Ueda, Taeko
Kurita, Tomoko
Matsuura, Yusuke
Yoshino, Kiyoshi
Source :
Oncology Letters. Jul2024, Vol. 28 Issue 1, pN.PAG-N.PAG. 1p.
Publication Year :
2024

Abstract

Cytokine release syndrome (CRS) is a systemic inflammatory condition caused by an excessive immune response and cytokine overproduction. CRS is a life-threatening condition that is often associated with chimeric antigen receptor T-cell therapy. Despite the increased use of immune checkpoint inhibitors (ICIs), ICI-induced CRS remains rare. The present study describes a case of CRS that occurred after the administration of ICIs for recurrent adenocarcinoma of the uterine cervix. A 49-year-old woman received paclitaxel, carboplatin and pembrolizumab for recurrent cervical adenocarcinoma. On day 27 of the third cycle, the patient was admitted with a fever and suspected pyelonephritis. The following day, hypotension, upper respiratory symptoms and myalgia of the extremities were noted, and the left ventricular ejection fraction (LVEF) was decreased to 20%. Multiorgan failure (MOF) occurred, and the patient received ventilator support and continuous hemodiafiltration. Rhabdomyolysis, pancreatitis, erythema multiforme and enteritis were observed. CRS was diagnosed based on elevated ferritin and IL-6 levels. Steroid pulse therapy was administered; however, the MOF did not improve and the anti-IL-6-receptor monoclonal antibody tocilizumab (TOC) was administered. Subsequently, the LVEF improved to 50%, and the patient was removed from the ventilator on day 4 and from the continuous hemodiafiltration unit on day 6 after TOC administration. The patient was discharged on day 21. In conclusion, considering that ICI-induced CRS is a rare but severe complication, fever and other systemic conditions following ICI administration should be monitored. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17921074
Volume :
28
Issue :
1
Database :
Academic Search Index
Journal :
Oncology Letters
Publication Type :
Academic Journal
Accession number :
177774761
Full Text :
https://doi.org/10.3892/ol.2024.14463