Article
作者: Blaney, Susan ; Baxter, Patricia ; Mei, Zhuyong ; Brenner, Malcolm K. ; Rooney, Cliona M ; Parikh, Kathan ; White, Mark ; Parsons, D. Williams ; Heslop, Helen E ; Blaney, Susan ; Stuckert, Austin ; Lin, Frank Y ; Baxter, Patricia ; Shum, Thomas ; Kinnear, Darryl ; Mehta, Birju ; Tat, Candise ; Aldave, Guillermo ; Thakkar, Sachin ; Shekar, Meghan ; Aldave, Guillermo ; Heslop, Helen E. ; Wang, Tao ; Anastas, Jamie ; Anastas, Jamie ; Scherer, Lauren ; Wang, Tao ; Wu, Meng-Fen ; Brenner, Malcolm K ; Grilley, Bambi ; Hicks, John ; Grilley, Bambi ; Hicks, John ; Rooney, Cliona M. ; Ruggieri, Lucia ; Lapteva, Natalia ; Lindsay, Holly B ; Malbari, Fatema ; Malbari, Fatema ; Zhang, Huimin ; Moeller, Karen ; Lin, Frank Y. ; Omer, Bilal ; Chintagumpala, Murali ; Moeller, Karen ; Omer, Bilal ; Chintagumpala, Murali ; Lindsay, Holly B. ; Roy, Angshumoy ; Parsons, D Williams ; Blessing, Melissa M. ; Roy, Angshumoy ; Major, Angela
PURPOSE:T cells modified with chimeric antigen receptors (CARTs) have demonstrated efficacy for hematologic malignancies; however, benefit for patients with CNS tumors has been limited. To enhance T cell activity against GD2+ CNS malignancies, we modified GD2-directed CART cells (GD2.CARTs) with a constitutively active interleukin (IL)-7 receptor (C7R-GD2.CARTs).
METHODS:
Patients age 1-21 years with H3K27-altered diffuse midline glioma (DMG) or other recurrent GD2-expressing CNS tumors were eligible for this phase I trial (ClinicalTrials.gov identifier:
NCT04099797
). All subjects received standard-of-care adjuvant radiation therapy or chemotherapy before study enrollment. The first treatment cohort received GD2.CARTs alone (1 × 10
7
cells/m
2
), and subsequent cohorts received C7R-GD2.CARTs at two dose levels (1 × 10
7
cells/m
2
; 3 × 10
7
cells/m
2
). Standard lymphodepletion with cyclophosphamide and fludarabine was included at all dose levels.
RESULTS:
Eleven patients (age 4-18 years) received therapy without dose-limiting toxicity. The GD2.CART cohort did not experience toxicity, but had disease progression after brief improvement of residual neurologic deficits (≤3 weeks). The C7R-GD2.CART cohort developed grade 1 tumor inflammation–associated neurotoxicity in seven of eight (88%) cases, controllable with anakinra. Cytokine release syndrome was observed in six of eight (75%, grade 1 in all but one patient) and associated with increased circulating IL-6 and IP-10 (
P
< .05). Patients receiving C7R-GD2.CARTs experienced temporary improvement from baseline neurologic deficits (range, 2 to >12 months), and seven of eight (88%) remained eligible for additional treatment cycles (range 2-4 cycles). Partial responses by iRANO criteria were observed in two of seven (29%) patients with DMG treated by C7R-GD2.CARTs.
CONCLUSION:Intravenous GD2.CARTs with and without C7R were well tolerated. Patients treated with C7R-GD2.CARTs exhibited transient improvement of neurologic deficits and increased circulating cytokines/chemokines. Treatment with C7R-GD2.CARTs represents a novel approach warranting further investigation for children with these incurable CNS cancers.