Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Immune checkpoint inhibitors (ICIs) have significantly improved the survival of patients with advanced tumors. However, immune-related adverse events (irAEs) caused by ICIs, especially high-grade irAEs, are of growing concern. High-grade multisystem irAEs due to toripalimab, a programmed cell death-1 (PD-1) inhibitor, have been rarely reported. Two patients with malignant metastatic tumors were treated with anti-PD-1 immunotherapy. However, both patients developed high-grade multisystem irAEs based on myocarditis, with chest discomfort and malaise as the main clinical manifestation. Both patients had an elevation of cardiac enzymes, abnormal electrocardiography and left ventricular wall motion. Patient 2 was also diagnosed with organizing pneumonia. Immunotherapy was suspended. High-dose intravenous methylprednisolone was immediately initiated. The patients' symptoms were significantly relieved in a short period of time. Immunosuppressants were discontinued at the 6th month follow-up in patient 1 without relapse. However, patient 2 was lost to follow up due to financial reasons. To the best of our knowledge, this is the first report regarding ICI-associated myocarditis-pneumonia due to toripalimab, indicating the significance of early recognition and management of high-grade multisystem irAEs in clinical practice.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9732722PMC
http://dx.doi.org/10.3389/fcvm.2022.1036603DOI Listing

Publication Analysis

Top Keywords

high-grade multisystem
12
multisystem iraes
12
immune-related adverse
8
adverse events
8
iraes
5
multisystem
4
multisystem immune-related
4
events toripalimab
4
toripalimab cases-based
4
cases-based review
4

Similar Publications

Lemierre's Syndrome Presenting with Multisystem Complications in a Child: A Case Report and Literature Review.

Reports (MDPI)

January 2025

Department of Pediatrics, College of Medicine, Qassim University, Buraydah 52571, Saudi Arabia.

Lemierre's syndrome, also known as the "forgotten disease", is a rare clinical syndrome of septic thrombophlebitis associated with morbidity and mortality. This study reports on a 6-year-old boy diagnosed with Lemierre's syndrome, providing an in-depth case analysis and a comprehensive review of the current literature on this uncommon condition. : A 6-year-old boy was admitted to the pediatric intensive care unit (PICU) with septic shock, presenting with a high-grade fever of 39.

View Article and Find Full Text PDF

Background: Abdominal solid organ (ASO) trauma of the spleen, kidney, and liver is common in children and often accompanies other traumatic injuries, posing significant clinical challenges. Non-operative management (NOM) is preferred according to current guidelines for both low- and high-grade lesions when hemodynamic stability is achievable. Aggressive surgical treatment can lead to chronic organ dysfunction, surgical related complications and long-term sequelae, while NOM failure may result in critical bleeding and multiorgan failure.

View Article and Find Full Text PDF

Objective: Ovarian cancers exhibit very heterogeneous genetic and genomic aberrations with various pathogenetic and prognostic values. Chromosome 22 abnormalities, including del(22q) and duplications, are genetic multisystemic disorders, most commonly affecting cardiovascular, immune, and gastrointestinal systems, while tumors are rarely reported.

Methods: In this case report, we described a patient with 22q11.

View Article and Find Full Text PDF

Loeys-Dietz syndrome (LDS) is a heritable connective tissue disorder with variable expressivity. It is a multisystemic condition mainly characterized by a propensity for arterial aneurysms and dissections, skeletal manifestations, hypertelorism, bifid uvula, craniosynostosis, and cutaneous features. While LDS has significant clinical overlap with other heritable connective tissue disorders such as Marfan syndrome, the ocular manifestations of LDS have not yet been well characterized.

View Article and Find Full Text PDF

Background: Sarcoidosis is a systemic inflammatory disease of unknown aetiology characterized by the formation of non-caseating granulomas. Cardiac involvement occurs in up to 30% of cases but only manifests clinically in 5%. In young patients presenting with high-grade atrioventricular block, infiltrative processes such as sarcoidosis should be considered in the differential diagnosis.

View Article and Find Full Text PDF