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GD2-CART01 for Relapsed or Refractory High-Risk Neuroblastoma

医学 神经母细胞瘤 耐火材料(行星科学) 免疫疗法 内科学 细胞因子释放综合征 临床试验 自杀基因 胃肠病学 嵌合抗原受体 外科 遗传增强 癌症 细胞培养 基因 物理 天体生物学 生物 化学 生物化学 遗传学
作者
Francesca Del Bufalo,Biagio De Angelis,Ignazio Caruana,Giada Del Baldo,Maria Antonietta De Ioris,Annalisa Serra,Angela Mastronuzzi,Maria Giuseppina Cefalo,Daria Pagliara,Matteo Amicucci,Giuseppina Li Pira,G Leone,Valentina Bertaina,Matilde Sinibaldi,Stefano Di Cecca,Marika Guercio,Zeinab Abbaszadeh,Laura Iaffaldano,Monica Gunetti,Stefano Iacovelli,Rossana Bugianesi,Stefania Macchia,Mattia Algeri,Pietro Merli,Federica Galaverna,Rachid Abbas,Maria Carmen Garganese,Maria Felicia Villani,Giovanna Stefania Colafati,F Bonetti,Marco Rabusin,Katia Perruccio,Veronica Folsi,Concetta Quintarelli,Franco Locatelli
出处
期刊:The New England Journal of Medicine [New England Journal of Medicine]
卷期号:388 (14): 1284-1295 被引量:122
标识
DOI:10.1056/nejmoa2210859
摘要

Immunotherapy with chimeric antigen receptor (CAR)-expressing T cells that target the disialoganglioside GD2 expressed on tumor cells may be a therapeutic option for patients with high-risk neuroblastoma.In an academic, phase 1-2 clinical trial, we enrolled patients (1 to 25 years of age) with relapsed or refractory, high-risk neuroblastoma in order to test autologous, third-generation GD2-CAR T cells expressing the inducible caspase 9 suicide gene (GD2-CART01).A total of 27 children with heavily pretreated neuroblastoma (12 with refractory disease, 14 with relapsed disease, and 1 with a complete response at the end of first-line therapy) were enrolled and received GD2-CART01. No failure to generate GD2-CART01 was observed. Three dose levels were tested (3-, 6-, and 10×106 CAR-positive T cells per kilogram of body weight) in the phase 1 portion of the trial, and no dose-limiting toxic effects were recorded; the recommended dose for the phase 2 portion of the trial was 10×106 CAR-positive T cells per kilogram. Cytokine release syndrome occurred in 20 of 27 patients (74%) and was mild in 19 of 20 (95%). In 1 patient, the suicide gene was activated, with rapid elimination of GD2-CART01. GD2-targeted CAR T cells expanded in vivo and were detectable in peripheral blood in 26 of 27 patients up to 30 months after infusion (median persistence, 3 months; range, 1 to 30). Seventeen children had a response to the treatment (overall response, 63%); 9 patients had a complete response, and 8 had a partial response. Among the patients who received the recommended dose, the 3-year overall survival and event-free survival were 60% and 36%, respectively.The use of GD2-CART01 was feasible and safe in treating high-risk neuroblastoma. Treatment-related toxic effects developed, and the activation of the suicide gene controlled side effects. GD2-CART01 may have a sustained antitumor effect. (Funded by the Italian Medicines Agency and others; ClinicalTrials.gov number, NCT03373097.).
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