TY - JOUR
T1 - GD2-CART01 for Relapsed or Refractory High-Risk Neuroblastoma
AU - Del, Bufalo F.
AU - De, Angelis B.
AU - Caruana, I.
AU - Del, Baldo G.
AU - De, Ioris M. A.
AU - Serra, A.
AU - Mastronuzzi, Angela
AU - Cefalo, M. G.
AU - Pagliara, D.
AU - Amicucci, M.
AU - Li, Pira G.
AU - Leone, G.
AU - Bertaina, V.
AU - Sinibaldi, M.
AU - Di, Cecca S.
AU - Guercio, M.
AU - Abbaszadeh, Z.
AU - Iaffaldano, L.
AU - Gunetti, M.
AU - Iacovelli, S.
AU - Bugianesi, R.
AU - Macchia, S.
AU - Algeri, M.
AU - Merli, P.
AU - Galaverna, F.
AU - Abbas, R.
AU - Garganese, M. C.
AU - Villani, M. F.
AU - Colafati, G. S.
AU - Bonetti, F.
AU - Rabusin, M.
AU - Perruccio, K.
AU - Folsi, V.
AU - Quintarelli, C.
AU - Locatelli, Franco
PY - 2023
Y1 - 2023
N2 - Background: 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. Methods: 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). Results: 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. Conclusions: 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.).
AB - Background: 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. Methods: 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). Results: 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. Conclusions: 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.).
KW - CAR T GD2
KW - neuroblastoma
KW - CAR T GD2
KW - neuroblastoma
UR - https://publicatt.unicatt.it/handle/10807/233287
UR - https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85151776363&origin=inward
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85151776363&origin=inward
U2 - 10.1056/NEJMoa2210859
DO - 10.1056/NEJMoa2210859
M3 - Article
SN - 0028-4793
VL - 388
SP - 1284
EP - 1295
JO - THE NEW ENGLAND JOURNAL OF MEDICINE
JF - THE NEW ENGLAND JOURNAL OF MEDICINE
IS - 14
ER -