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Frontline Risk-Adapted Optimization of Novel Targeted Immunotherapy Evaluation in High-Risk MCL (FRONTIER)

2026年4月28日 更新者:Miltenyi Biomedicine GmbH

Phase II Multicenter Trial of MB-CART2019.1 (Zamtocabtagene Autoleucel) Therapy as Frontline Consolidation for High-Risk Mantle Cell Lymphoma

FRONTIER 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 (MCL) participants

調査の概要

詳細な説明

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.

研究の種類

介入

入学 (推定)

52

段階

  • フェーズ2

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究連絡先のバックアップ

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

Inclusion Criteria:

  • Diagnosis of MCL requires histologic confirmation by either overexpression of cyclin D1 OR presence of t(11;14) (q13; q32) translocation

    1. 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.
    2. 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:

    1. High risk MIPI-c (as calculated by https://www.european-mcl.net/home/scores-mipi-mipi-c-19.html)
    2. Simplified MIPI high-risk ≥6.2
    3. TP53 mutation OR ≥50% TP53 expression by IHC
    4. Complex Karyotype [e.g. 3 or more cytogenetic abnormalities, excluding the presence or absence of t(11:14)]
    5. Ki67≥ 50%
    6. Blastoid or pleomorphic histology with Ki-67 ≥30%
    7. Leptomeningeal Disease at diagnosis
    8. 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:

    1. CD20 antibody alone does not count towards a cycle of treatment
    2. Induction cycles do not have to be identical
    3. For BTKis and/or lenalidomide a cycle is defined as 14-28 days and will be based on institutional treatment regimens.
    4. Intrathecal chemotherapy will not count towards a cycle of treatment
    5. 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:

    1. Adequately treated basal cell or squamous cell carcinoma (adequate wound healing is required prior to study entry)
    2. In situ carcinoma of the cervix or breast, treated curatively and without evidence of recurrence for at least 2 years prior to the study
    3. 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
    4. A primary malignancy which has been completely resected / treated with curative intent and in complete remission of ≥ 2 years
    5. 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

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:なし
  • 介入モデル:単一グループの割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:シングル、オープンラベル
リンパ除去化学療法
リンパ除去化学療法
chimeric antigen receptor T-cell (CAR-T) therapy

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Progression-free survival (PFS)
時間枠: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

二次結果の測定

結果測定
メジャーの説明
時間枠
Treatment Response
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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
時間枠:1 year post-infusion
Relapse/progression events will be determined per Lugano criteria.
1 year post-infusion
IEC Related Toxicities
時間枠: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)
時間枠: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

協力者と研究者

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出版物と役立つリンク

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便利なリンク

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年9月1日

一次修了 (推定)

2029年9月1日

研究の完了 (推定)

2030年3月1日

試験登録日

最初に提出

2026年4月28日

QC基準を満たした最初の提出物

2026年4月28日

最初の投稿 (実際)

2026年5月6日

学習記録の更新

投稿された最後の更新 (実際)

2026年5月6日

QC基準を満たした最後の更新が送信されました

2026年4月28日

最終確認日

2026年4月1日

詳しくは

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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