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OncoMatch/Clinical Trials/NCT06172296

Dinutuximab With Chemotherapy, Surgery and Stem Cell Transplantation for the Treatment of Children With Newly Diagnosed High Risk Neuroblastoma

Is NCT06172296 recruiting? Yes, currently enrolling (May 2026). This Phase 3 trial studies multiple treatments for ganglioneuroblastoma, nodular.

Phase 3RecruitingNational Cancer Institute (NCI)NCT06172296Data as of May 2026

Treatment: Carboplatin · Cisplatin · Cyclophosphamide · Dinutuximab · Doxorubicin · Etoposide · Irinotecan · Isotretinoin · Melphalan · Temozolomide · Thiotepa · Topotecan · VincristineThis 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.

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Extracted eligibility criteria

Cancer type

Neuroblastoma

Biomarker criteria

Required: MYCN amplification

Disease stage

Required: Stage INRG STAGE L1, INRG STAGE L2, INRG STAGE M, INRG STAGE MS (INRG)

Excluded: Stage INRG STAGE L2, MYCN NON-AMPLIFIED NBL (≥ 547 DAYS OF AGE), INRG STAGE M, MYCN NON-AMPLIFIED NBL (365-546 DAYS OF AGE)

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; 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

Prior therapy

No prior treatment (treatment-naive required)

Lab requirements

Kidney function

Serum creatinine based on age/sex (see table); or 24-hour urine creatinine clearance ≥ 70 mL/min/1.73 m^2; or GFR ≥ 70 mL/min/1.73 m^2 by direct measurement

Liver function

Total bilirubin ≤ 1.5 x upper limit of normal (ULN) for age; SGPT (ALT) ≤ 10 x ULN (ULN for SGPT (ALT) set to 45 U/L)

Cardiac function

Shortening fraction of ≥ 27% by echocardiogram, or ejection fraction of ≥ 50% by echocardiogram or radionuclide angiogram

A serum creatinine based on age/sex as follows... or a 24-hour urine creatinine clearance ≥ 70 mL/min/1.73 m^2 or a GFR ≥ 70 mL/min/1.73 m^2... Total bilirubin ≤ 1.5 x upper limit of normal (ULN) for age; SGPT (ALT) ≤ 10 x ULN; Shortening fraction of ≥ 27% by echocardiogram, or ejection fraction of ≥ 50% by echocardiogram or radionuclide angiogram

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Children's Hospital of Alabama · Birmingham, Alabama
  • USA Health Strada Patient Care Center · Mobile, Alabama
  • Banner Children's at Desert · Mesa, Arizona
  • Phoenix Childrens Hospital · Phoenix, Arizona
  • Banner University Medical Center - Tucson · Tucson, Arizona

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