Your browser doesn't support javascript.
loading
Need for standardization of cytokine profiling in CAR T cell therapy.
Biery, D Nathan; Turicek, David P; Diorio, Caroline; Schroeder, Brett A; Shah, Nirali N.
Affiliation
  • Biery DN; Pediatric Oncology Branch, Center for Cancer Research (CCR), National Cancer Institute (NCI), NIH, Bethesda, MD, USA; George Washington University School of Medicine, Washington, DC, USA.
  • Turicek DP; Pediatric Oncology Branch, Center for Cancer Research (CCR), National Cancer Institute (NCI), NIH, Bethesda, MD, USA; Division of Biology and Biomedical Sciences, Washington University, St. Louis, MO, USA.
  • Diorio C; Division of Oncology, Center for Childhood Cancer Research, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Schroeder BA; Department of Hematology and Medical Oncology, CCR, NCI, NIH, Bethesda, MD, USA.
  • Shah NN; Pediatric Oncology Branch, Center for Cancer Research (CCR), National Cancer Institute (NCI), NIH, Bethesda, MD, USA. Electronic address: nirali.shah@nih.gov.
Mol Ther ; 32(9): 2979-2983, 2024 Sep 04.
Article in En | MEDLINE | ID: mdl-38532629
ABSTRACT
With expansion of chimeric antigen receptor (CAR) T cell therapy and broader utilization of anti-cytokine directed therapeutics for toxicity mitigation, the routine assessment of cytokines may enhance understanding of toxicity profiles, guide therapeutic interventions, and facilitate cross-trial comparisons. As specific cytokine elevations can correlate with and provide insights into CARcell toxicity, mitigation strategies, and response, we explored the reporting of cytokine detection methods and assessed for the correlation of cytokines to cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS) across clinical trials. In this analysis, we reviewed 21 clinical trials across 60 manuscripts that featured a US Food and Drug Administration-approved CARcell construct or one of its predecessors. We highlight substantial variability and limited reporting of cytokine measurement platforms and panels used across CARcell clinical trials. Specifically, across 60 publications, 28 (46.7%) did not report any cytokine data, representing 6 of 21 (28.6%) clinical trials. In the 15 trials reporting cytokine data, at least 4 different platforms were used. Furthermore, correlation of cytokines with ICANS, CRS, and CRS severity was limited. Considering the fundamental role of cytokines in CARcell toxicity, our manuscript supports the need to establish standardization of cytokine measurements as a key biomarker essential to improving outcomes of CARcell therapy.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Clinical Trials as Topic / Cytokines / Immunotherapy, Adoptive / Receptors, Chimeric Antigen / Cytokine Release Syndrome Limits: Humans Language: En Journal: Mol Ther Journal subject: BIOLOGIA MOLECULAR / TERAPEUTICA Year: 2024 Document type: Article Affiliation country: United States Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Clinical Trials as Topic / Cytokines / Immunotherapy, Adoptive / Receptors, Chimeric Antigen / Cytokine Release Syndrome Limits: Humans Language: En Journal: Mol Ther Journal subject: BIOLOGIA MOLECULAR / TERAPEUTICA Year: 2024 Document type: Article Affiliation country: United States Country of publication: United States