Abstract

Over the past decade, chimeric antigen receptor (CAR) T-cell therapy has significantly improved the outlook for many patients with relapsed and/or refractory B-cell malignancies. The use of CAR T-cell therapy and other therapeutic immune effector cells will likely continue to expand with the development of other targets and use in solid tumors. Although these therapies have shown significant promise in the treatment of some malignancies, they can be associated with unique toxicities including cytokine release syndrome and immune effector cell-associated neurotoxicity syndrome which can be fatal if not identified early and treated appropriately. An understanding of how best to manage the toxicities associated with CAR T-cell therapy is continually evolving. Institutions providing CAR T-cell therapy have undergone changes in infrastructure and staffing models in order to safely care for patients receiving this novel therapy. As members of a multi-disciplinary health care team, advanced practice providers play significant roles in caring for this patient population and must be well-versed in the recognition, grading, and appropriate management of CAR T-cell therapy-related toxicities as these providers care for patients in multiple settings across the continuum of care.

Highlights

  • Chimeric Antigen Receptor (CAR) T-cell therapy is an adoptive cell therapy that has dramatically improved outcomes in some patients with relapsed or refractory B-cell malignancies

  • This review will include a focused discussion regarding risk factors, differential diagnoses, and guidelines for grading cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS), as well as long-term and late effects of chimeric antigen receptor (CAR) T-cell therapy and ways Advanced practice providers (APPs) contribute to providing optimal care

  • Karschnia et al found that decreased platelets at the time of CAR T-cell infusion correlated with an increased grade of ICANS, possibly indicating that heavily pre-treated patients tend to have an increased risk of treatment-related adverse events [38]

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Summary

INTRODUCTION

Chimeric Antigen Receptor (CAR) T-cell therapy is an adoptive cell therapy that has dramatically improved outcomes in some patients with relapsed or refractory B-cell malignancies. This review will include a focused discussion regarding risk factors, differential diagnoses, and guidelines for grading cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS), as well as long-term and late effects of CAR T-cell therapy and ways APPs contribute to providing optimal care. Karschnia et al found that decreased platelets at the time of CAR T-cell infusion correlated with an increased grade of ICANS, possibly indicating that heavily pre-treated patients tend to have an increased risk of treatment-related adverse events [38]. This finding may act as a future biomarker of blood-brain barrier disturbance which could suggest a pathogenesis of ICANS [38]. For patients who develop frequent viral infections and have low levels of immunoglobulin G, monthly infusions of intravenous immunoglobulin G

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