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Table 1 Summary of reported CD19-negative relapse in trials of anti-CD19 CAR-T cells for B-ALL

From: New development in CAR-T cell therapy

Treating institute

Patient populations

Construct (scFv-Hinge-TM-CD-SD)

Gene transfer method

Conditioning therapy

Infused cell dose

Responses observed

Reported relapse

MSKCC [26]

Adult

33

32 evaluable for response

SJ25C1-CD28-CD3ζ

Retrovirus

Cy or Cy/Flu

1–3 × 106 CAR+ T cells/kg

CR: 29/32 (91%)

14 relapse with 2 CD19− relapse

Upenn [24]

Pediatric and young adult

59

FMC63-CD8α-4-1BB-CD3ζ

Lentivirus

Investigator’s choice

107–108 cells/kg with a transduction efficiency of 2.3–45%

CR: 55/59 (93%)

20 relapse with 13 CD19− relapse

NCI [25]

Young adult

38

FMC63-CD28-CD3ζ

Retrovirus

Cy/Flu or FLAG or IE

1 or 3 × 106 CAR+ T cells/kg

CR: 23/38 (61%)

2 CD19− relapse

FHCRC [5]

Adult

30

29 evaluable for response

FMC63-IgG4

CD28-4-1BB-CD3ζ

Lentivirus

Cy ± etoposide or Cy/Flu

2 × 105 or 2 × 106 or 2 × 107 CAR+ T cells/kg

(1:1 CD4+:CD8+)

CR: 27/29 (93%)

9 relapse with 2 CD19− relapse

  1. MSKCC Memorial Sloan Kettering Cancer Center, Upenn University of Pennsylvania, NCI US National Cancer Institute, FHCRC Fred Hutchinson Cancer Research Center, scFv single-chain variable fragment, B-ALL B cell acute lymphoblastic leukemia, Cy cyclophosphamide, Flu fludarabine, FIAG fludarabine + Ara-c + G-CSF, IE ifosfamide/etoposide, CR complete remission, CAR-T chimeric antigen receptor-modified T cell