2021
DOI: 10.2214/ajr.21.26091
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CAR T-Cell Therapy: An Update for Radiologists

Abstract: The publication of this Accepted Manuscript is provided to give early visibility to the contents of the article, which will undergo additional copyediting, typesetting, and review before it is published in its final form. During the production process, errors may be discovered that could affect the content of the Accepted Manuscript. All legal disclaimers that apply to the journal pertain. The reader is cautioned to consult the definitive version of record before relying on the contents of this document.

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Cited by 24 publications
(20 citation statements)
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References 74 publications
(125 reference statements)
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“…In contrast, toxicities related to CAR-T cell therapy can be serious, as CAR-T cell therapy can cause cytokine release syndrome (CRS), immune effector cell-associated neurotoxicity syndrome (ICANS), or hemophagocytic lymphohistiocytosis/macrophage activation syndrome ( Table 5 ) [ 31 32 ]. The typical time for CRS is approximately 1–5 days after infusion, with an approximate incidence of 42%–100% and severe incidence in 0%–46% of patients.…”
Section: Imaging Biomarkers For Immunotherapymentioning
confidence: 99%
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“…In contrast, toxicities related to CAR-T cell therapy can be serious, as CAR-T cell therapy can cause cytokine release syndrome (CRS), immune effector cell-associated neurotoxicity syndrome (ICANS), or hemophagocytic lymphohistiocytosis/macrophage activation syndrome ( Table 5 ) [ 31 32 ]. The typical time for CRS is approximately 1–5 days after infusion, with an approximate incidence of 42%–100% and severe incidence in 0%–46% of patients.…”
Section: Imaging Biomarkers For Immunotherapymentioning
confidence: 99%
“…The typical time for CRS is approximately 1–5 days after infusion, with an approximate incidence of 42%–100% and severe incidence in 0%–46% of patients. ICAN usually occurs within 1–3 weeks after infusion and in 0%–50% of severe cases [ 32 33 ]. Although CRS and ICANS are usually concomitant and correlated, they rarely occur independently.…”
Section: Imaging Biomarkers For Immunotherapymentioning
confidence: 99%
“…The patient's T-cells are modified in vitro to express chimeric antigen receptors that can detect tumorspecific antigens. When these modified T-cells are reintroduced to the patient, they recognize the tumor cells and activate the body's immune system to attack these cells [24]. Positron emission tomography/CT (PET/CT) or Positron emission tomography/ magnetic resonance imaging (PET/MRI) is the preferred imaging modality to monitor CAR Tcell migration and response to treatment.…”
Section: Types Of Immunotherapymentioning
confidence: 99%
“…Brain CT and MRI are usually negative, however, they are essential to rule out other neurologic etiologies. Occasionally, brain MRI can show T2 and FLAIR hyperintensity, vasogenic edema, leptomeningeal enhancement, multifocal microhemorrhages, and cortical infarcts [24].…”
Section: Car-t Cell-associated Toxicitymentioning
confidence: 99%
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