Testing a New Combination of Anti-cancer Drugs in Patients Newly Diagnosed With Ewing Sarcoma Who Have Cancer That Has Spread to Other Parts of the Body

Part of paid clinical trials in Birmingham, Alabama.

Sponsor
Children's Oncology Group
Study ID
NCT06820957
Phase
PHASE2/PHASE3
Status
Active Not Recruiting

Conditions

  • CIC-Rearranged Sarcoma
  • Metastatic Ewing Sarcoma
  • Metastatic High Grade Sarcoma
  • Metastatic Undifferentiated Round Cell Sarcoma
  • Metastatic Undifferentiated Sarcoma, Not Otherwise Specified
  • Round Cell Sarcoma With EWSR1-non-ETS Fusion
  • Sarcoma With BCOR Genetic Alterations

Eligibility Criteria

Sex
ALL
Age
12 Years - 50 Years
Healthy Volunteers
Not accepted

Interventions

  • Biopsy Procedure — PROCEDURE
    Undergo bone marrow aspiration and biopsy
  • Biospecimen Collection — PROCEDURE
    Undergo tissue and/or blood sample collection
  • Bone Marrow Aspiration — PROCEDURE
    Undergo bone marrow aspiration and biopsy
  • Bone Marrow Biopsy — PROCEDURE
    Undergo bone marrow aspiration and biopsy
  • Computed Tomography — PROCEDURE
    Undergo CT
  • Cyclophosphamide — DRUG
    Given IV
  • Doxorubicin Hydrochloride — DRUG
    Given IV
  • Echocardiography Test — PROCEDURE
    Undergo echocardiography
  • Etoposide — DRUG
    Given IV
  • Fludeoxyglucose F-18 — OTHER
    Given FDG
  • Ifosfamide — DRUG
    Given IV
  • Irinotecan Hydrochloride — DRUG
    Given IV
  • Magnetic Resonance Imaging — PROCEDURE
    Undergo MRI
  • Positron Emission Tomography — PROCEDURE
    Undergo FDG PET
  • Questionnaire Administration — OTHER
    Ancillary studies
  • Radiation Therapy — RADIATION
    Undergo radiation
  • Regorafenib — DRUG
    Given PO
  • Surgical Procedure — PROCEDURE
    Undergo surgery
  • Vincristine Sulfate — DRUG
    Given IV

Study Details

This phase II/III trial compares the effect of vincristine, irinotecan, and regorafenib (VIrR) in combination with vincristine, doxorubicin, cyclophosphamide (VDC), ifosfamide and etoposide (IE) to usual treatment with VDC/IE for the treatment of newly diagnosed Ewing sarcoma or other round cell sarcomas that have spread from where they first started (primary site) to other places in the body (metastatic). Vincristine is in a class of medications called vinca alkaloids. It works by stopping tumor cells from growing and dividing and may kill them. Irinotecan is in a class of antineoplastic medications called topoisomerase I inhibitors. It blocks a certain enzyme needed for cell division and deoxyribonucleic acid (DNA) repair and may kill tumor cells. Regorafenib, a type of kinase inhibitor and a type of antiangiogenesis agent, blocks certain proteins, which may help keep tumor cells from growing. It may also prevent the growth of new blood vessels that tumors need to grow. Doxorubicin is in a class of medications called anthracyclines. Doxorubicin damages the cell's DNA and may kill tumor cells. It also blocks a certain enzyme needed for cell division and DNA repair. Cyclophosphamide is in a class of medications called alkylating agents. It works by damaging the cell's DNA and may kill tumor cells. It may also lower the body's immune response. Ifosfamide, a type of alkylating agent and a type of antimetabolite, attaches to DNA in cells and may kill tumor cells. Etoposide is in a class of medications known as podophyllotoxin derivatives. It blocks a certain enzyme needed for cell division and DNA repair and may kill tumor cells. Giving VIrR/VDC/IE may be more effective than usual treatment with VDC/IE in treating patients with newly diagnosed metastatic Ewing sarcoma or other round cell sarcomas.

Key Dates

Start date
Nov 10, 2025
Status verified
Feb 2026
Primary completion
Dec 31, 2027
Completion
Dec 31, 2027

Study Design

Enrollment
437 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Active Comparator: Regimen A (VDC/IE)
    See Detailed description
  • Experimental: Regimen B (VIrR/VDC/IE)
    See Detailed Description

Primary Outcome Measure

Time to event-free survival (EFS) post-Consolidation I (C1) [ Time Frame: From randomization to progression or relapse, diagnosis of a second malignant neoplasm, death, or last patient contact, whichever occurs first, assessed up to 10 years ]

Locations (9)

FacilityCityStateZIPSite coordinators
Children's Hospital of AlabamaBirminghamAlabama35233-
Kapiolani Medical Center for Women and ChildrenHonoluluHawaii96826-
Lurie Children's Hospital-ChicagoChicagoIllinois60611-
Saint Jude Midwest AffiliatePeoriaIllinois61637-
NYU Langone Hospital - Long IslandMineolaNew York11501-
Saint Christopher's Hospital for ChildrenPhiladelphiaPennsylvania19134-
Prisma Health Richland HospitalColumbiaSouth Carolina29203-
BI-LO Charities Children's Cancer CenterGreenvilleSouth Carolina29605-
East Tennessee Childrens HospitalKnoxvilleTennessee37916-

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