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临床试验/NCT06172296
NCT06172296招募中3 期

A Phase 3 Study of Dinutuximab Added to Intensive Multimodal Therapy for Children With Newly Diagnosed High-Risk Neuroblastoma

National Cancer Institute (NCI)310 个研究点 分布在 1 个国家目标入组 478 人开始时间: 2024年4月19日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
招募中
入组人数
478
试验地点
310
主要终点
Event free survival (EFS)

研究概览

简要总结

This phase III trial tests how well the addition of dinutuximab to Induction chemotherapy along with standard of care surgical resection of the primary tumor, radiation, stem cell transplantation, and immunotherapy works for treating children with newly diagnosed high-risk neuroblastoma. Dinutuximab is a monoclonal antibody that binds to a molecule called GD2, which is found on the surface of neuroblastoma cells, but is not present on many healthy or normal cells in the body. When dinutuximab binds to the neuroblastoma cells, it helps signal the immune system to kill the tumor cells. This helps the cells of the immune system kill the cancer cells, this is a type of immunotherapy. When chemotherapy and immunotherapy are given together, during the same treatment cycle, it is called chemoimmunotherapy. This clinical trial randomly assigns patients to receive either standard chemotherapy and surgery or chemoimmunotherapy (chemotherapy plus dinutuximab) and surgery during Induction therapy. Chemotherapy drugs administered during Induction include, cyclophosphamide, topotecan, cisplatin, etoposide, vincristine, and doxorubicin. These drugs work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing or by stopping them from spreading. Upon completion of 5 cycles of Induction therapy, a disease evaluation is completed to determine how well the treatment worked. If the tumor responds to therapy, patients receive a tandem transplantation with stem cell rescue. If the tumor has little improvement or worsens, patients receive chemoimmunotherapy on Extended Induction. During Extended Induction, dinutuximab is given with irinotecan, temozolomide. Patients with a good response to therapy move on to Consolidation therapy, when very high doses of chemotherapy are given at two separate points to kill any remaining cancer cells. Following, transplant, radiation therapy is given to the site where the cancer originated (primary site) and to any other areas that are still active at the end of Induction. The final stage of therapy is Post-Consolidation. During Post-Consolidation, dinutuximab is given with isotretinoin, with the goal of maintaining the response achieved with the previous therapy. Adding dinutuximab to Induction chemotherapy along with standard of care surgical resection of the primary tumor, radiation, stem cell transplantation, and immunotherapy may be better at treating children with newly diagnosed high-risk neuroblastoma.

详细描述

PRIMARY OBJECTIVE:

I. To determine if the event-free survival (EFS) of patients with newly diagnosed high-risk neuroblastoma assigned to early chemoimmunotherapy during Induction differs from that of patients who are not assigned to treatment that includes early chemoimmunotherapy.

SECONDARY OBJECTIVES:

I. To determine if early chemoimmunotherapy during Induction therapy improves end of Induction (EOI) response rates and overall survival (OS) for patients with newly diagnosed high-risk neuroblastoma.

II. To determine response rates, EFS, and OS following an Extended Induction regimen with chemoimmunotherapy in patients with progressive disease or a poor response to Induction therapy.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
— 至 30 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Patients must be enrolled on APEC14B1 and have consented to testing through the Molecular Characterization Initiative (MCI), prior to enrollment on ANBL2131
  • ≤ 30 years at the time of initial diagnosis with high-risk disease
  • * Must have a diagnosis of neuroblastoma (NBL) or ganglioneuroblastoma (nodular) verified by tumor pathology analysis or demonstration of clumps of tumor cells in bone marrow with elevated urinary catecholamines
  • Newly diagnosed, high risk neuroblastoma (HRNBL) defined as one of the following:
  • Any age with International Neuroblastoma Risk Group (INRG) Stage L2, MS, or M and MYCN amplification
  • Age ≥ 547 days and INRG stage M regardless of biologic features (clinical MYCN testing not required prior to enrollment)
  • Any age initially diagnosed with INRG Stage L1 MYCN amplified NBL who have progressed to stage M without systemic chemotherapy
  • Age ≥ 547 days of age initially diagnosed with INRG Stage L1, L2, or MS who have progressed to stage M without systemic chemotherapy (clinical MYCN testing not required prior to enrollment)
  • Patients must have a body surface area (BSA) ≥ 0.25 m^2
  • No prior anti-cancer therapy except as outlined below:
  • Patients initially recognized to have high-risk disease treated with topotecan/cyclophosphamide initiated on an emergent basis and within allowed timing, and with consent
  • Patients observed or treated with a single cycle of chemotherapy per a low or intermediate risk neuroblastoma regimen (e.g., as per ANBL0531, ANBL1232 or similar) for what initially appeared to be non-high-risk disease but subsequently found to meet the criteria
  • Patients who received localized emergency radiation to sites of life threatening or function-threatening disease prior to or immediately after establishment of the definitive diagnosis
  • Human immunodeficiency virus (HIV) -infected patients on effective anti-retroviral therapy with undetectable viral load within 6 months are eligible for this trial
  • A serum creatinine based on age/sex as follows:
  • 1 month to < 6 months: Male 0.4 mg/dL and female 0.4mg/dL
  • 6 months to < 1 year: Male 0.5 mg/dL and female 0.5 mg/dL
  • 1 to < 2 years: Male 0.6 mg/dL and female 0.6 mg/dL
  • 2 to < 6 years: Male 0.8 mg/dL and female 0.8 mg/dL
  • 6 to < 10 years: Male 1 mg/dL and female 1 mg/dL
  • 10 to < 13 years: Male 1.2 mg/dL and female 1.2 mg/dL
  • 13 to < 16 years: Male 1.5 mg/dL and female 1.4 mg/dL
  • ≥ 16 years: Male 1.7 mg/dL and female 1.4 mg/dL
  • The threshold creatinine values were derived from the Schwartz formula for estimating glomerular filtration rate (GFR) utilizing child length and stature data published by the Centers for Disease Control (CDC)
  • or a 24-hour urine creatinine clearance ≥ 70 mL/min/1.73 m^2 or
  • or a GFR ≥ 70 mL/min/1.73 m^
  • GFR must be performed using direct measurement with a nuclear blood sampling method or direct small molecule clearance method (iothalamate or other molecule per institutional standard)
  • Note: Estimated GFR (eGFR) from serum creatinine, cystatin C or other estimates are not acceptable for determining eligibility
  • Total bilirubin ≤ 1.5 x upper limit of normal (ULN) for age
  • Serum glutamic pyruvic transaminase (SGPT) (Alanine aminotransferase [ALT]) ≤ 10 x ULN*
  • Note: For the purpose of this study, the ULN for SGPT (ALT) has been set to the value of 45 U/L
  • * Shortening fraction of ≥ 27% by echocardiogram, or
  • Ejection fraction of ≥ 50% by echocardiogram or radionuclide angiogram
  • Ability to tolerate Peripheral Blood Stem Cell (PBSC) collection:
  • No known contraindication to PBSC collection. Examples of contraindications might be a weight or size less than the collecting institution finds feasible, or a physical condition that would limit the ability of the child to undergo apheresis catheter placement (if necessary) and/or the apheresis procedure

排除标准

  • Patients who are 365-546 days of age with INRG Stage M and MYCN non-amplified NBL, irrespective of additional biologic features
  • Patients ≥ 547 days of age with INRG Stage L2, MYCN non-amplified NBL, regardless of additional biologic features
  • Patients with known bone marrow failure syndromes
  • Patients on chronic immunosuppressive medications (e.g., tacrolimus, cyclosporine, corticosteroids) for reasons other than prevention/treatment of allergic reactions and adrenal replacement therapy are not eligible. Topical and inhaled corticosteroids are acceptable
  • Patients with a primary immunodeficiency syndrome who require ongoing immune globulin replacement therapy
  • Female patients who are pregnant since fetal toxicities and teratogenic effects have been noted for several of the study drugs. A pregnancy test is required prior to enrollment for female patients of childbearing potential
  • Lactating females who plan to breastfeed their infants
  • Sexually active patients of reproductive potential who have not agreed to use an effective contraceptive method for the duration of their study participation
  • All patients and/or their parents or legal guardians must sign a written informed consent
  • All institutional, food and drug administration (FDA), and National Cancer Institute (NCI) requirements for human studies must be met

研究组 & 干预措施

Arm A (SOC treatment)

Active Comparator

See detailed description

干预措施: Carboplatin (Drug)

Arm A (SOC treatment)

Active Comparator

See detailed description

干预措施: Cyclophosphamide (Drug)

Arm A (SOC treatment)

Active Comparator

See detailed description

干预措施: Dinutuximab (Biological)

Arm A (SOC treatment)

Active Comparator

See detailed description

干预措施: Doxorubicin (Drug)

Arm A (SOC treatment)

Active Comparator

See detailed description

干预措施: Echocardiography Test (Procedure)

Arm A (SOC treatment)

Active Comparator

See detailed description

干预措施: Etoposide (Drug)

Arm A (SOC treatment)

Active Comparator

See detailed description

干预措施: Magnetic Resonance Imaging (Procedure)

Arm A (SOC treatment)

Active Comparator

See detailed description

干预措施: Melphalan (Drug)

Arm B (Dinutuximab in induction)

Experimental

See detailed description

干预措施: Carboplatin (Drug)

Arm B (Dinutuximab in induction)

Experimental

See detailed description

干预措施: Cisplatin (Drug)

Arm B (Dinutuximab in induction)

Experimental

See detailed description

干预措施: Computed Tomography (Procedure)

Arm A (SOC treatment)

Active Comparator

See detailed description

干预措施: Biospecimen Collection (Procedure)

Arm A (SOC treatment)

Active Comparator

See detailed description

干预措施: Topotecan (Drug)

Arm B (Dinutuximab in induction)

Experimental

See detailed description

干预措施: Bone Marrow Biopsy (Procedure)

Arm B (Dinutuximab in induction)

Experimental

See detailed description

干预措施: Magnetic Resonance Imaging (Procedure)

Arm B (Dinutuximab in induction)

Experimental

See detailed description

干预措施: Survey Administration (Other)

Arm B (Dinutuximab in induction)

Experimental

See detailed description

干预措施: Tumor Resection (Procedure)

Arm B (Dinutuximab in induction)

Experimental

See detailed description

干预措施: Multigated Acquisition Scan (Procedure)

Arm A (SOC treatment)

Active Comparator

See detailed description

干预措施: Radionuclide Imaging (Procedure)

Arm B (Dinutuximab in induction)

Experimental

See detailed description

干预措施: Dinutuximab (Biological)

Arm B (Dinutuximab in induction)

Experimental

See detailed description

干预措施: Topotecan (Drug)

Arm B (Dinutuximab in induction)

Experimental

See detailed description

干预措施: Vincristine (Drug)

Arm B (Dinutuximab in induction)

Experimental

See detailed description

干预措施: Thiotepa (Drug)

Arm B (Dinutuximab in induction)

Experimental

See detailed description

干预措施: Temozolomide (Drug)

Arm A (SOC treatment)

Active Comparator

See detailed description

干预措施: Irinotecan (Drug)

Arm B (Dinutuximab in induction)

Experimental

See detailed description

干预措施: Irinotecan (Drug)

Arm B (Dinutuximab in induction)

Experimental

See detailed description

干预措施: Isotretinoin (Drug)

Arm A (SOC treatment)

Active Comparator

See detailed description

干预措施: Isotretinoin (Drug)

Arm A (SOC treatment)

Active Comparator

See detailed description

干预措施: Multigated Acquisition Scan (Procedure)

Arm B (Dinutuximab in induction)

Experimental

See detailed description

干预措施: Etoposide (Drug)

Arm B (Dinutuximab in induction)

Experimental

See detailed description

干预措施: Echocardiography Test (Procedure)

Arm B (Dinutuximab in induction)

Experimental

See detailed description

干预措施: Doxorubicin (Drug)

Arm A (SOC treatment)

Active Comparator

See detailed description

干预措施: Survey Administration (Other)

Arm A (SOC treatment)

Active Comparator

See detailed description

干预措施: Tumor Resection (Procedure)

Arm A (SOC treatment)

Active Comparator

See detailed description

干预措施: Bone Marrow Biopsy (Procedure)

Arm A (SOC treatment)

Active Comparator

See detailed description

干预措施: FDG-Positron Emission Tomography and Computed Tomography Scan (Procedure)

Arm A (SOC treatment)

Active Comparator

See detailed description

干预措施: Hematopoietic Cell Transplantation (Procedure)

Arm A (SOC treatment)

Active Comparator

See detailed description

干预措施: Leukapheresis (Procedure)

Arm B (Dinutuximab in induction)

Experimental

See detailed description

干预措施: Bone Marrow Aspiration (Procedure)

Arm B (Dinutuximab in induction)

Experimental

See detailed description

干预措施: Biospecimen Collection (Procedure)

Arm B (Dinutuximab in induction)

Experimental

See detailed description

干预措施: Radiation Therapy (Radiation)

Arm B (Dinutuximab in induction)

Experimental

See detailed description

干预措施: Radionuclide Imaging (Procedure)

Arm B (Dinutuximab in induction)

Experimental

See detailed description

干预措施: FDG-Positron Emission Tomography and Computed Tomography Scan (Procedure)

Arm B (Dinutuximab in induction)

Experimental

See detailed description

干预措施: Hematopoietic Cell Transplantation (Procedure)

Arm A (SOC treatment)

Active Comparator

See detailed description

干预措施: Vincristine (Drug)

Arm A (SOC treatment)

Active Comparator

See detailed description

干预措施: Temozolomide (Drug)

Arm A (SOC treatment)

Active Comparator

See detailed description

干预措施: Thiotepa (Drug)

Arm B (Dinutuximab in induction)

Experimental

See detailed description

干预措施: Leukapheresis (Procedure)

Arm B (Dinutuximab in induction)

Experimental

See detailed description

干预措施: Melphalan (Drug)

Arm B (Dinutuximab in induction)

Experimental

See detailed description

干预措施: Cyclophosphamide (Drug)

Arm A (SOC treatment)

Active Comparator

See detailed description

干预措施: Cisplatin (Drug)

Arm A (SOC treatment)

Active Comparator

See detailed description

干预措施: Bone Marrow Aspiration (Procedure)

Arm A (SOC treatment)

Active Comparator

See detailed description

干预措施: Computed Tomography (Procedure)

Arm A (SOC treatment)

Active Comparator

See detailed description

干预措施: Radiation Therapy (Radiation)

结局指标

主要结局

Event free survival (EFS)

时间窗: Up to 3 years

EFS time is calculated from time of randomization to Arms A or B to first episode of disease relapse or progression, second malignancy, or death, or until last contact if no event has occurred.

次要结局

  • End of Induction (EOI) response rate(From randomization to end of extended Induction, up to 12 months)
  • Overall survival (OS)(Up to 3 years)
  • Incidence of adverse events(Up to 2 years)
  • GD2 expression(Up to 12 months)

研究者

申办方类型
Nih
责任方
Sponsor

研究点 (310)

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