Table 3 Clinical trials of CAR T-cell therapy in recurrent GB.

From: Immunotherapy for recurrent glioblastoma: practical insights and challenging prospects

Trials

No.

Delivery routes

Target

Molecular characteristic

Toxicity

Phase

Results

NCT00730613

3

IC

IL13Rα2

NA

No grade 3 or higher

I

1 pt with reduced IL13Rα2 expression;

1 pt with an increment of TNV

NCT01109095

17

IV

Her2

NA

No dose-limiting toxic effects

I

1 pt with PR > 9 m;

7pts with SD for 8w to 29 m;

3pts with SD for 24-29 m; mOS: 24.5 m

NCT02442297

28

IC

Her2

NA

NA

I

NA

NCT02208362

1

IC then IV

IL13Rα2

MGMT non met

IDH1 WT

No grade 3 or higher

I

Regression of all tumors;

increment of cytokines and immune cells;

clinical response for 7.5 m

NCT02209376

10

IV

EGFRvIII

MGMT non met

No off-tumor toxicity or cytokine release syndrome

I

1 pt with SD > 18 m; mOS:251days

increment of inhibitory molecules and Treg

NCT02844062

20

IC

EGFRvIII

NA

NA

I

NA

NCT02937844

20

IV

Anti-PD-L1 CSR T cells

NA

NA

I

NA

NCT03170141

20

IV or IC

EGFRvIII

NA

NA

I

NA

NCT03389230

42

IT

HER2-CD3ζ-CD19t

NA

NA

I

NA

NCT03283631

24

IC

EGFRvIII

NA

NA

I

NA

NCT04045847

31

IC

CD147

NA

NA

I

NA

NCT04385173

12

IT

CD276

NA

NA

I

NA

NCT04077866

40

IT

CD276

NA

NA

I/II

NA

NCT04214392

36

IV

CD28-CD3ζ-CD19t

MMP2+

NA

I

NA

NCT04077866

100

IC

B7-H3

NA

No off-tumor toxicity

II

Effectively control tumor growth

  1. IC infusions into tumor cavity, IV intravenous, IT intratumoral or intracerebroventricular injection.