Effects of an Initial Anti-CD19 CAR T-cell Therapy on Subsequent Anti-CD22 CAR T-cell Manufacturing and Clinical Outcomes in Patients with Relapsed/Refractory LBCL

  • Yi Jiun Su
  • , Anne Marijn Kramer
  • , Mark P. Hamilton
  • , Neha Agarwal
  • , Hrishikesh K. Srinagesh
  • , John H. Baird
  • , Bita Sahaf
  • , Adam Kuo
  • , Zachary J. Ehlinger
  • , Moksha H. Desai
  • , Skyler P. Rietberg
  • , Ramya Tunuguntla
  • , Shabnum Patel
  • , Harshini Chinnasamy
  • , Nikolaos Gkitsas-Long
  • , Dorota D. Klysz
  • , Annie Kathleen Brown
  • , Sushma Bharadwaj
  • , Saurabh Dahiya
  • , Melody Smith
  • Lori Muffly, Crystal L. Mackall, Zinaida Good, Steven A. Feldman, David B. Miklos, Matthew J. Frank*
*Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

1 Scopus citations

Abstract

Late leukapheresis (>6 months after CAR19) resulted in less residual CAR19, higher CAR22 CD4+ naïve T and TCM cells, less TEM cells, and higher CD8+ TCM cells, but similar clinical outcomes to those with early leukapheresis. CAR22 responses were associated with higher transduction efficiency and CD8+ TCM and less CD8+ TEM cells.

Original languageEnglish
Pages (from-to)733-747
Number of pages15
JournalCancer Discovery
Volume15
Issue number4
DOIs
StatePublished - 02 04 2025
Externally publishedYes

Bibliographical note

©2025 American Association for Cancer Research.

Keywords

  • Humans
  • Immunotherapy, Adoptive/methods
  • Antigens, CD19/immunology
  • Receptors, Chimeric Antigen/immunology
  • Sialic Acid Binding Ig-like Lectin 2/immunology
  • Male
  • Treatment Outcome
  • Female
  • Middle Aged
  • Receptors, Antigen, T-Cell
  • Leukemia, Lymphocytic, Chronic, B-Cell/therapy
  • Aged
  • Leukapheresis

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