Anti-GD2 CAR T Cells in Pediatric Patients Affected by High Risk and/or Relapsed/Refractory Neuroblastoma or Other GD2-positive Solid Tumors
Phase I/II Study of Anti-GD2 Chimeric Antigen Receptor-Expressing T Cells in Pediatric Patients Affected by High Risk and/or Relapsed/Refractory Neuroblastoma or Other GD2-positive Solid Tumors
The purpose of this study is to test the safety and efficacy of GD2-CART01, a CAR T cell treatment targeting GD2 in paediatric or young adult patients with High Risk and/or relapsed/refractory Neuroblastoma.
A small exploratory cohort of patients with GD2-positive tumors other than Neuroblastoma has also been included.
Aperçu de l'étude
Statut
Statut
Les conditions
Les conditions
Intervention / Traitement
Intervention / Traitement
Description détaillée
The study will consist of 2 phases, a Phase I or dose escalation phase and a Phase II or expansion phase. Paediatric or young adult patients with relapsed High Risk and/or relapsed/refractory Neuroblastoma will be enrolled in the study.
After completion of the phase I portion of the study, a small cohort of patients with GD2-positive tumors other than Neuroblastoma has also been included.
Eligible patients will undergo leukapheresis in order to harvest T cells, which will be manufactured to obtain the autologous CAR T product GD2-CART01, a GD2-targeting CAR T product. Briefly, the patients will be treated with a lymphodepleting regimen containing conventional chemotherapic agents and subsequently will receive a single infusion of GD2-CART01. Moreover, the product contains a suicide gene safety switch (namely inducible Caspase 9): in case of relevant toxicities, the patient will receive the dimerizing agent in order to activate the apoptotic pathway in the infused T cells.
After infusion of CAR T cells, the patients will enter a 5-year active follow-up period.
Type d'étude
Type d'étude
Inscription (Estimé)
Inscription
Phase
Phase
- Phase 2
- La phase 1
Contacts et emplacements
Lieux d'étude
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-
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Roma, Italie
- Ospedale Pediatrico Bambino Gesù
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Critères de participation
Critère d'éligibilité
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
Phase I The patient must meet the following eligibility inclusion criteria to be enrolled to receive treatment in the Phase I study.
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Diagnosis of NBL that have been treated with frontline therapy and is judged to be incurable, based upon the following criteria:
- Relapse after first-line treatment, proved by a positive 123-I-mMIBG-scan
- Persistence/progression of disease after the initiation of the upfront treatment
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Patients must have measurable or evaluable disease at the time of treatment enrollment, as shown by bone marrow biopsy/aspirate, US or CT/MRI scan or by 123-I-mMIBG scan.
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Recover from the toxic effect of previous chemotherapies: grade 4 and or 3 non-hematologic toxicities must have resolved to grade ≤2; if some effects of the therapies have become chronic (i.e. treatment associated thrombocytopenia), the patient must be clinically stable, according to the opinion of the treating physicians, and meet all other eligibility criteria.
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Age: 12 months -18 years.
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Voluntary informed consent is given. For subjects < 18 years old their legal guardian must give informed consent. Pediatric subjects will be included in age appropriate discussion and verbal assent will be obtained for those greater than or equal to 12 years of age, when appropriate.
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Clinical performance status: Patients > 16 years of age: Karnofsky greater than or equal to 60%; Patients less than or equal to 16 years of age: Lansky scale greater than or equal to 60%.
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Patients of child-bearing or child-fathering potential must be willing to practice birth control from the time of enrollment on this study and for four months after receiving the preparative regimen.
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Females of child-bearing potential must have a negative pregnancy test because of the potentially dangerous effects on the fetus.
Phase II
The patient must meet the following eligibility inclusion criteria to be enrolled to receive treatment in the Phase II study.
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Diagnosis of NBL that have been treated with frontline therapy and is judged to be incurable, based upon the following criteria:
- Relapse after first-line treatment, proved by a positive MIBG-scan
- Persistence/progression of disease after the initiation of the upfront treatment
OR
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Diagnosis of extremely High Risk NBL at high risk of relapse, defined by stage III/IV and Myc-N amplification, at the end of the first-line treatment according to the Standard of Care, even if NED.
OR
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Diagnosis of GD2+ tumors other than Neuroblastoma, considered incurable with conventional treatments by the treating physician.
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Patients with relapsed/refractory disease must have measurable or evaluable disease at the time of treatment enrollment, as shown by bone marrow biopsy/aspirate, US or CT/MRI scan or by MIBG-scan.
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Recover from the toxic effect of previous chemotherapies: grade 4 and or 3 non-hematologic toxicities must have resolved to grade ≤2; if some effects of the therapies have become chronic (i.e. treatment associated thrombocytopenia), the patient must be clinically stable, according to the opinion of the treating physicians, and meet all other eligibility criteria.
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Age: 12 months - 18 years.
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Voluntary informed consent is given. For subjects < 18 years old their legal guardian must give informed consent. Pediatric subjects will be included in age appropriate discussion and verbal assent will be obtained for those greater than or equal to 12 years of age, when appropriate.
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Clinical performance status: Patients > 16 years of age: Karnofsky greater than or equal to 60%; Patients less than or equal to 16 years of age: Lansky scale greater than or equal to 60%.
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Patients of child-bearing or child-fathering potential must be willing to practice birth control from the time of enrollment on this study and for four months after receiving the preparative regimen.
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Females of child-bearing potential must have a negative pregnancy test because of the potentially dangerous effects on the fetus
Exclusion Criteria:
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Pregnant or lactating women
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Severe, uncontrolled active intercurrent infections
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Active hepatitis B or hepatitis C infection
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HIV infection
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Rapidly progressive disease with life-expectancy < 6 weeks
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History of grade 3 or 4 hypersensitivity to murine protein-containing products
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Hepatic function: Inadequate liver function defined as total bilirubin > 4x upper limit of normal (ULN) or transaminase (ALT and AST) > 6 x ULN based on age and laboratory specific normal ranges
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Renal function: serum creatinine > 3x ULN for age.
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Blood oxygen saturation < 90%.
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Cardiac function: Left ventricular ejection fraction lower than 45% by ECHO.
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Marrow function: ANC lower than 500/mm3 and/or platelets lower than 20.000 (not reached by transfusion).
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Congestive heart failure, cardiac arrhythmia, psychiatric illness, or social situations that would limit compliance with study requirements or in the opinion of the PI would pose an unacceptable risk to the subject.
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Untreated CNS metastasis; patients with previous CNS tumor involvement that has been treated and is stable for at least 6 weeks following completion of therapy are eligible.
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Concurrent or recent prior therapies, before infusion:
- Systemic steroids (at a dose equivalent to or greater 2 mg/kg prednisone) in the 2 weeks before infusion. Recent or current use of inhaled/topical/non-absorbable steroids is not exclusionary.
- Systemic chemotherapy in the 2 weeks preceding infusion.
- Immunosuppressive agents less than or equal to 30 days.
- Radiation therapy must have been completed at least 3 weeks prior to enrollment.
- I131-MIBG therapy must have been completes at least 6 weeks prior to enrollment
- Anti-GD2 murine monoclonal antibody (ch14.18 antibody) in the 2 weeks preceding infusion
- Other anti-neoplastic investigational agents currently or within 30 days prior to start of protocol therapy;
- Exceptions:
- Subjects receiving steroid therapy at physiologic replacement doses only are allowed provided there has been no increase in dose for at least 2 weeks prior to starting apheresis
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Patient-derived GD2-CART01 production failure.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: N / A
- Modèle interventionnel: Affectation à un seul groupe
- Masquage: Aucun (étiquette ouverte)
Nombre de bras
Armes et Interventions
Groupe de participants / BrasGroupe de participants / Bras |
Intervention / TraitementIntervention / Traitement |
|---|---|
|
Expérimental: GD2-CART01
After a lymphodepleting regimen the patients will receive 1.0 to 10.0 x 10⁶/kg GD2 Chimeric Antigen Receptor (CAR) positive T cells. |
Following a lymphodepleting treatment with conventional chemotherapy, patients will be treated with 1.0 to 10.0 x 10⁶/kg GD2 Chimeric Antigen Receptor (CAR) positive T cells as a single dose. |
Que mesure l'étude ?
Principaux critères de jugement
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Phase I - Identification of the dose limiting toxicity (DLT)
Délai: 4 weeks after T cell infusion
|
Toxicity will be assessed according to the NCI Common Terminology Criteria for Adverse Events (CTCAE) scale, version 4 and the number of patients experiencing DLT will be evaluated |
4 weeks after T cell infusion
|
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Phase II - Antitumor effect
Délai: Up to 6 months after T cell infusion
|
Assessment of Best Overall Response (BOR) |
Up to 6 months after T cell infusion
|
Mesures de résultats secondaires
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Temps de progression (TTP)
Délai: Jusqu'à 5 ans après la perfusion de lymphocytes T
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Jusqu'à 5 ans après la perfusion de lymphocytes T
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|
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Survie sans événement (EFS)
Délai: Jusqu'à 5 ans après la perfusion de lymphocytes T
|
Jusqu'à 5 ans après la perfusion de lymphocytes T
|
|
|
Survie globale (SG)
Délai: Jusqu'à 5 ans après la perfusion de lymphocytes T
|
Jusqu'à 5 ans après la perfusion de lymphocytes T
|
|
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In vivo persistence/expansion of infused CAR T cell
Délai: UP to 5 years
|
Detection of infused CAR T cell in the peripheral and bone marrow blood |
UP to 5 years
|
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Serum cytokine profiling
Délai: First 2 weeks after T cell infusion
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Assessment of the seric cytokines profile |
First 2 weeks after T cell infusion
|
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Disease outcome according to INRC vs irRC
Délai: Up to 5 years
|
Tumor response assessment through the two different criteria |
Up to 5 years
|
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Elimination of CAR T cell through iC9 in case of toxicity
Délai: Up to 15 years
|
Assessment of the kinetic of CAR T cell elimination after infusion of the dimerizer |
Up to 15 years
|
Collaborateurs et enquêteurs
Parrainer
Parrainer
Publications et liens utiles
Publications générales
- Tumino N, Weber G, Besi F, Del Bufalo F, Bertaina V, Paci P, Quatrini L, Antonucci L, Sinibaldi M, Quintarelli C, Maggi E, De Angelis B, Locatelli F, Moretta L, Vacca P, Caruana I. Polymorphonuclear myeloid-derived suppressor cells impair the anti-tumor efficacy of GD2.CAR T-cells in patients with neuroblastoma. J Hematol Oncol. 2021 Nov 12;14(1):191. doi: 10.1186/s13045-021-01193-0.
- Locatelli F, Pagliara D, De Ioris MA, Becilli M, Del Baldo G, Serra A, Mastronuzzi A, Cefalo MG, Li Pira G, Leone G, Bertaina V, Fabozzi F, Di Nardo M, Rosignoli C, D'Andrea ML, Crocoli A, Vennarini S, Sinibaldi M, Di Cecca S, Guercio M, Iaffaldano L, Lucarelli B, Algeri M, Merli P, Colafati GS, De Angelis B, Quintarelli C, Del Bufalo F. GD2-targeting CAR T cells in high-risk neuroblastoma: a phase 1/2 trial. Nat Med. 2025 Nov;31(11):3689-3699. doi: 10.1038/s41591-025-03874-6. Epub 2025 Aug 21.
- Yeku OO, Longo DL. CAR T Cells for Neuroblastoma. N Engl J Med. 2023 Apr 6;388(14):1328-1331. doi: 10.1056/NEJMe2300317. No abstract available.
- Del Bufalo F, De Angelis B, Caruana I, Del Baldo G, De Ioris MA, Serra A, Mastronuzzi A, Cefalo MG, Pagliara D, Amicucci M, Li Pira G, Leone G, Bertaina V, Sinibaldi M, Di Cecca S, Guercio M, Abbaszadeh Z, Iaffaldano L, Gunetti M, Iacovelli S, Bugianesi R, Macchia S, Algeri M, Merli P, Galaverna F, Abbas R, Garganese MC, Villani MF, Colafati GS, Bonetti F, Rabusin M, Perruccio K, Folsi V, Quintarelli C, Locatelli F; Precision Medicine Team-IRCCS Ospedale Pediatrico Bambino Gesu. GD2-CART01 for Relapsed or Refractory High-Risk Neuroblastoma. N Engl J Med. 2023 Apr 6;388(14):1284-1295. doi: 10.1056/NEJMoa2210859.
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Début de l'étude
Achèvement primaire (Estimé)
Achèvement primaire
Achèvement de l'étude (Estimé)
Achèvement de l'étude
Dates d'inscription aux études
Première soumission
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Première publication
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour publiée
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
- Tumeurs
- Tumeurs par type histologique
- Tumeurs, glandulaires et épithéliales
- Tumeurs, neuroépithéliales
- Tumeurs neuroectodermiques
- Tumeurs, cellules germinales et embryonnaires
- Tumeurs, tissu nerveux
- Tumeurs, tissus conjonctifs et mous
- Tumeurs neuroectodermiques, primitives, périphériques
- Tumeurs neuroectodermiques primitives
- Tumeurs, tissu osseux
- Tumeurs, tissu conjonctif
- Neuroblastome
- Sarcome d'Ewing
- Sarcome
- Ostéosarcome
Autres numéros d'identification d'étude
Autres numéros d'identification d'étude
- GD2CAR01
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Informations sur les médicaments et les dispositifs, documents d'étude
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