Guideline-based strategies to identify severe cytokine release syndrome in COVID-19 and cancer immunotherapy using large-scale electronic health records. [PDF]
Robert PA +7 more
europepmc +1 more source
The Immuno-oncology-Induced Cytokine Release Syndrome Patient Diary: A Content-Valid, Patient-Reported Outcome Measure. [PDF]
Wells ET +9 more
europepmc +1 more source
Digital Biomarkers of Cytokine Release Syndrome: Scoping Review and Ontology Development of the Role and Relevance of Digital Measures Using a Mixed Methods Approach. [PDF]
Medberry CJ +24 more
europepmc +1 more source
A Case Report of Sustained Cytokine Release Syndrome Due to Glofitamab and Literature Review. [PDF]
Yang J, Shen Q, Ke X, Liu W, Yang P.
europepmc +1 more source
Machine learning-based predictive model for high- grade cytokine release syndrome in chimeric antigen receptor T-cell therapy. [PDF]
Yu X +10 more
europepmc +1 more source
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Druggable Targets in Cytokine Release Syndromes
Clinical Cancer Research, 2023Summary Bispecific T-cell engagers and chimeric antigen receptor T cells share the problem of eliciting acute systemic inflammation episodes known as cytokine release syndrome. Knowledge on the sequential waves of cytokines that can be neutralized with clinically available agents is crucial to prevent or treat this condition without ...
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Cytokine Release Syndrome Biology and Management
The Cancer Journal, 2021Abstract The successful application of chimeric antigen receptor (CAR) T cells for the treatment of relapsed and refractory B-cell malignancies has ushered in a new frontier for the immunotherapy of cancer. Despite its successes, CAR T-cell therapy presents several challenges.
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Infectious Disease Clinics of North America, 2022Both cytokine release syndrome (CRS) and sepsis are clinical syndromes rather than distinct diseases and share considerable overlap. It can often be challenging to distinguish between the two, but it is important given the availability of targeted treatment options.
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Nature Medicine, 2018Complete leukemic responses to chimeric antigen receptor–modified T cells are invariably accompanied by severe toxicity. Recently developed animal models allow mechanistic dissection and prevention of toxicity without loss of therapeutic benefit.
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