Optimization of a flow cytometry test for routine monitoring of B cell maturation antigen targeted CAR in peripheral blood

Author:

Lee Won‐Ho1,Graham Charlotte E.12,Wiggin Hadley R.1,Nolan Hannah K.1,Graham Kiana J.1,Korell Felix12,Leick Mark B.12,Barselau Alexis L.1,Emmanuel‐Alejandro Estelle1,Trailor Michael A.1,Gildea Juliane M.1,Preffer Frederic3,Frigault Matthew J.12,Maus Marcela V.12,Gallagher Kathleen M. E.12

Affiliation:

1. Cellular Immunotherapy Program, Cancer Center Massachusetts General Hospital Boston Massachusetts USA

2. Department of Pathology and Department of Medicine Harvard Medical School Boston Massachusetts USA

3. Department of Pathology Massachusetts General Hospital Boston Massachusetts USA

Abstract

AbstractChimeric antigen receptor (CAR) modified T cell therapies targeting BCMA have displayed impressive activity in the treatment of multiple myeloma. There are currently two FDA licensed products, ciltacabtagene autoleucel and idecabtagene vicleucel, for treating relapsed and refractory disease. Although correlative analyses performed by product manufacturers have been reported in clinical trials, there are limited options for reliable BCMA CAR T detection assays for physicians and researchers looking to explore it as a biomarker for clinical outcome. Given the known association of CAR T cell expansion kinetics with toxicity and response, being able to quantify BCMA CAR T cells routinely and accurately in the blood of patients can serve as a valuable asset. Here, we optimized an accurate and sensitive flow cytometry test using a PE‐conjugated soluble BCMA protein, with a lower limit of quantitation of 0.19% of CD3+ T cells, suitable for use as a routine assay for monitoring the frequency of BCMA CAR T cells in the blood of patients receiving either ciltacabtagene autoleucel or idecabtagene vicleucel.

Publisher

Wiley

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1. Issue highlights—May 2024;Cytometry Part B: Clinical Cytometry;2024-05

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