- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07569965
Frontline Risk-Adapted Optimization of Novel Targeted Immunotherapy Evaluation in High-Risk MCL (FRONTIER)
Phase II Multicenter Trial of MB-CART2019.1 (Zamtocabtagene Autoleucel) Therapy as Frontline Consolidation for High-Risk Mantle Cell Lymphoma
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
This is a prospective, single arm, open label, multi-center, Phase II study of MB-CART2019.1 (Zamtocabtagene Autoleucel) therapy as frontline consolidation for high-risk Mantle Cell Lymphoma participants. Participants will be enrolled on the study after diagnosis and before the end of their second cycle of induction therapy.
Eligible patients will receive a single intravenous infusion of MB-CART2019.1 cells at a dose of 2.5x10^6 cells/kg following lymphodepleting chemotherapy. The goal is 52 participants in total who receive MB-CART2019.1 therapy. Additional participants may be screened, consented, registered, and treated in order to reach accrual goals. Participants will be followed on the trial for 1-year post-infusion. Assessment of survival annually through 15 years after infusion will be completed using the CIBMTR infrastructure.
Tipo di studio
Iscrizione (Stimato)
Fase
- Fase 2
Contatti e Sedi
Contatto studio
- Nome: Sadie Swift
- Numero di telefono: 617-218-0044
- Email: clinicaltrials@miltenyi.com
Backup dei contatti dello studio
- Nome: Erick Flores
- Numero di telefono: 617-218-0044
- Email: clinicaltrials@miltenyi.com
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
- Adulto
- Adulto più anziano
Accetta volontari sani
Descrizione
Inclusion Criteria:
Diagnosis of MCL requires histologic confirmation by either overexpression of cyclin D1 OR presence of t(11;14) (q13; q32) translocation
- Subject should have a tumor biopsy sample (at least 5 unstained slides of tissue or tissue block) available prior to MB-CART2019.1 infusion, preferably collected pre-induction.
- If archival tissue is not available, the patient may be enrolled after discussion with the protocol chair and/or protocol officer
High Risk Disease at diagnosis, defined as having at least ONE of the criteria below:
- High risk MIPI-c (as calculated by https://www.european-mcl.net/home/scores-mipi-mipi-c-19.html)
- Simplified MIPI high-risk ≥6.2
- TP53 mutation OR ≥50% TP53 expression by IHC
- Complex Karyotype [e.g. 3 or more cytogenetic abnormalities, excluding the presence or absence of t(11:14)]
- Ki67≥ 50%
- Blastoid or pleomorphic histology with Ki-67 ≥30%
- Leptomeningeal Disease at diagnosis
- NOTCH1 mutation
Received 2 cycles of appropriate systemic induction therapy, which includes a CD20 antibody +/- cytotoxic therapy +/- oral targeted therapy (e.g., BTKi, immunomodulatory imid drugs), with the following considerations:
- CD20 antibody alone does not count towards a cycle of treatment
- Induction cycles do not have to be identical
- For BTKis and/or lenalidomide a cycle is defined as 14-28 days and will be based on institutional treatment regimens.
- Intrathecal chemotherapy will not count towards a cycle of treatment
- Radiation therapy will not count towards a cycle of treatment
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 at screening. ECOG performance status of 2 at screening is allowed if the decrease in performance status is attributed to lymphoma
Disease response assessment of either complete response, partial response, or stable disease by Lugano 2014 criteria assessed by 18F-fluorodeoxyglucose (FDG)-positron emission tomography (PET)/computed tomography (CT) (preferred) or contrast enhanced CT scans including neck/chest/abdomen/pelvis [37] after 2 cycles of induction therapy. If the participant has history of CNS disease, then he/she must have no history of or active parenchymal disease on magnetic resonance imaging (MRI)
a. Leptomeningeal alone disease is allowable if it is not clinically progressive or worsening from baseline assessment
- A creatinine clearance (as estimated by direct urine collection, Chronic Kidney Disease Epidemiology Collaboration [CKD-EPI], or Cockcroft-Gault Equation or institutional standard) ≥ 45 mL/min
- Subjects of childbearing or child fathering potential must be willing to practice birth control from the time of enrollment on this study until the follow-up period of the study
Exclusion Criteria:
- Unable to give informed consent
- Any disease progression that occurs during the first 2 induction cycles
- A creatinine clearance (as estimated by direct urine collection, Chronic Kidney Disease Epidemiology Collaboration [CKD-EPI], or Cockcroft-Gault Equation or institutional standard) < 45 mL/min
- Cardiac ejection fraction (EF) < 45% as determined by an echocardiogram (ECHO) or Multigated Radionuclide Acquisition scan (MUGA) (if range is provided, the upper value of the range may be used for assessing eligibility)
- Resting O2 saturation < 92% on room air
- Serum alanine aminotransferase (ALT) / aspartate aminotransferase (AST) ≥ 5 times the Upper Limit of Normal (ULN) for age
- Total bilirubin >1.5 mg/dL, except in individuals with Gilbert's syndrome
- Absolute neutrophil count (ANC) < 1000/μL unless related to bone marrow infiltration by mantle cell lymphoma. No short-acting granulocyte colony-stimulating factor (G-CSF) use within 7 days of ANC evaluation
- Platelet count < 50,000/µL unless related to bone marrow infiltration or hypersplenism by mantle cell lymphoma. No transfusions within 7 days of assessment.
- Absolute CD3 count < 50/μL at screening
- Absolute lymphocyte count (ALC) < 100/μL within 7 days of apheresis
- Known history of infection with human immunodeficiency virus (HIV)
- Known active infection with hepatitis B (hepatitis B surface antigen [HBsAg] positive). If there is a history of treated hepatitis B, the viral load must be polymerase chain reaction (PCR) negative; antiviral prophylaxis is required if HBsAg negative and anti-hepatitis B core (HBc) positive
- Known active infection with hepatitis C virus (anti-HCV antibody positive). If patient has a positive hepatitis C antibody, the viral load must be undetectable per quantitative PCR and/or nucleic acid testing
- No seizure history within 6 months prior to enrollment
- Known history of cerebral vascular accident (CVA) within prior 12 months
- Known history or presence of autoimmune CNS disease, such as multiple sclerosis, optic neuritis or other immunologic /or inflammatory diseases
- Presence of active CNS disorder that, in the judgment of the investigator, may impair the ability to evaluate neurotoxicity
Uncontrolled bacterial, viral, or fungal infection at the time of enrollment.
a. Uncontrolled is defined as currently taking medication and with progression or no clinical improvement on adequate medical treatment
- Pregnant or breast-feeding woman
Previous or concurrent malignancy with the following exceptions:
- Adequately treated basal cell or squamous cell carcinoma (adequate wound healing is required prior to study entry)
- In situ carcinoma of the cervix or breast, treated curatively and without evidence of recurrence for at least 2 years prior to the study
- Adequately treated breast or prostate carcinoma on hormonal therapies such as Lupron or tamoxifen and in clinical remission of ≥ 2 years -or- low-grade untreated prostate cancer under observation
- A primary malignancy which has been completely resected / treated with curative intent and in complete remission of ≥ 2 years
- Subjects with prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with safety and efficacy assessment are eligible for this trial after discussion with protocol chair or protocol officer
- Severely immunocompromised participants e.g. due to current systemic treatment of non-neurologic autoimmune disease (e.g. Crohn's disease, rheumatoid arthritis, systemic lupus erythematosus)
- Medical condition requiring prolonged use of systemic corticosteroids equivalent to prednisone >10 mg/day.
- History of myocardial infarction, cardiac angioplasty or stenting, unstable angina, or other clinically significant cardiac disease within 6 months of enrollment
- For systemic therapy or radiation therapy, at least 2 weeks or 5 half-lives, whichever is shorter, must have elapsed at the time of scheduled leukapheresis
- BTKis can be continued through apheresis until one day prior to start of lymphodepletion
- Baseline neurologic deficits that would interfere with therapy or monitoring, determined using Immune Effector Cell-Associated Encephalopathy (ICE) Assessment at baseline
- History of severe immediate hypersensitivity reaction to any of the agents in this study
- Refusal or inability to participate in additional lentiviral gene therapy long-term follow-up (LTFU) protocol
- Prior CAR-T therapy for any indication or systemic gene-modifying therapy for B cell lymphoma
- Prior allogeneic stem cell transplant for any indication.
- Prior bispecific T cell engaging (BITE) antibodies for cancer therapy
- Prior T cell receptor-engineered T cell therapy
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: N / A
- Modello interventistico: Assegnazione di gruppo singolo
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Sperimentale: Etichetta singola aperta
|
Chemioterapia linfodepletiva
Chemioterapia linfodepletiva
chimeric antigen receptor T-cell (CAR-T) therapy
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Progression-free survival (PFS)
Lasso di tempo: 1 year post-infusion
|
The primary endpoint is PFS at 1-year following MB2019.1 CAR T cell infusion.
PFS is defined as the time interval from CAR T cell infusion until a PFS event occurs.
|
1 year post-infusion
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Treatment Response
Lasso di tempo: 1 year
|
Treatment response will be assessed using Lugano Criteria (Cheson et al, 2014).
Both best overall response and Day 90 response following CAR T cell infusion will be evaluated.
|
1 year
|
|
Overall Survival (OS)
Lasso di tempo: 1 year post-infusion
|
Events for OS include deaths from any cause.
OS is defined as the time interval from CAR T cell infusion until death.
|
1 year post-infusion
|
|
Duration of Complete Response (DOCR)
Lasso di tempo: 1 year post-infusion
|
DOCR is defined as the time from a participant's first achieving a CR until either a disease progression occurs per 2014 Lugano or IPCG criteria or death, whichever occurs first.
DOCR will be evaluated in the set of participants who achieve a CR.
|
1 year post-infusion
|
|
Non-relapse Mortality (NRM)
Lasso di tempo: 1 year post-infusion
|
Events for NRM include deaths without prior relapse/progression of the underlying malignancy.
Relapse/progression is treated as a competing risk for NRM.
|
1 year post-infusion
|
|
Relapse/progression
Lasso di tempo: 1 year post-infusion
|
Relapse/progression events will be determined per Lugano criteria.
|
1 year post-infusion
|
|
IEC Related Toxicities
Lasso di tempo: Up to 1 year post-infusion
|
CRS, ICANS, and IEC-HS will be determined per ASTCT criteria.
The incidence and severity of each of these toxicities within 28 days of CAR T cell infusion will be reported.
The incidence and severity of Grade 3 or higher ICANS occurring after Day 28 post-CAR T cell infusion will be reported.
|
Up to 1 year post-infusion
|
|
Event-free Survival (EFS)
Lasso di tempo: 1 year-post infusion
|
Events for EFS include clinical progression, additional anti-lymphoma treatment initiation (oral therapy, radiation) in the absence of clinical progression, and death.
EFS is defined as the time interval from CAR T cell infusion until an EFS event occurs.
|
1 year-post infusion
|
Collaboratori e investigatori
Pubblicazioni e link utili
Collegamenti utili
Studiare le date dei record
Studia le date principali
Inizio studio (Stimato)
Completamento primario (Stimato)
Completamento dello studio (Stimato)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
- Neoplasie
- Malattie del sistema immunitario
- Neoplasie per tipo istologico
- Malattie linfatiche
- Malattie linfoproliferative
- Disturbi immunoproliferativi
- Linfoma
- Malattie emiche e linfatiche
- Linfoma, cellule B
- Linfoma non Hodgkin
- Linfoma, cellule del mantello
- Prodotti chimici organici
- Idrocarburi
- Senape di fosforamide
- Composti di senape di azoto
- Composti di senape
- Idrocarburi, alogenati
- Fosforamidi
- Composti organofosfori
- Ciclofosfamide
- fludarabina
Altri numeri di identificazione dello studio
- PROJ112909
- U24HL138660 (Sovvenzione/contratto NIH degli Stati Uniti)
Piano per i dati dei singoli partecipanti (IPD)
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Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .