Cancers (Oct 2022)

Timely Leukapheresis May Interfere with the “Fitness” of Lymphocytes Collected for CAR-T Treatment in High Risk DLBCL Patients

  • Mirko Farina,
  • Marco Chiarini,
  • Camillo Almici,
  • Eugenia Accorsi Buttini,
  • Francesco Zuccalà,
  • Simone Piva,
  • Irene Volonghi,
  • Loris Poli,
  • Simona Bernardi,
  • Federica Colnaghi,
  • Federica Re,
  • Alessandro Leoni,
  • Nicola Polverelli,
  • Alessandro Turra,
  • Enrico Morello,
  • Anna Galvagni,
  • Daniele Moratto,
  • Duilio Brugnoni,
  • Chiara Cattaneo,
  • Emilio Ferrari,
  • Andrea Bianchetti,
  • Michele Malagola,
  • Alessandro Re,
  • Domenico Russo

DOI
https://doi.org/10.3390/cancers14215276
Journal volume & issue
Vol. 14, no. 21
p. 5276

Abstract

Read online

The development of chimeric antigen receptor (CAR)-T cell therapy has revolutionized the treatment of hematological diseases. However, approximately 60% of patients relapse after CAR-T cell therapy, and no clear cause for this failure has been identified. The objective of the Bio-CAR-T BS study (ClinicalTrials.gov: NCT05366569) is to improve our understanding of the lymphocyte harvest to maximize the quality of the CAR-T cell product. Of the 14 patients enrolled, 11 were diagnosed with DLBCL, 2 with PMBCL, and 1 with ALL. Five of 11 DLBCL patients met the criteria for “pre-emptive” Lymphocytes-apheresis (being at high risk of second relapse), and 6 were included in the standard-of-care Lymphocytes-apheresis group. Previous autologous stem cell transplantation (ASCT) and age were significantly different between the two groups. At the time of Lymphocyte-apheresis, patients in the “pre-emptive” group had more “fit” lymphocytes (higher CD4+/CD8+ ratio; higher naïve T cells levels) compared with standard group, probably due to the impact of ASCT. At the same time, also being older than 60 years results in a more “exhausted” lymphocyte profile. Overall, “pre-emptive” Ly-apheresis in DLBCL patients at high risk of relapse appears to be feasible and may allow the timely collection of “fit” lymphocytes for CAR-T cell manufacturing.

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