Chemo-immunotherapy in Patients Under 18 Years of Age With Bone and Soft Tissue Sarcomas

NCT ID: NCT06669013

Last Updated: 2024-11-01

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE3
• Total Enrollment: 40 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-05-20
• Study Completion Date: 2025-09-30

Brief Summary

Data from 40 patients are planned to be included in the study to randomize approximately 10 patients.

This study involves patients with advanced/metastatic GD2-positive rhabdomyosarcoma after progression on 1st line of chemotherapy, advanced/metastatic GD2-positive Ewing sarcoma after progression on 1st line of chemotherapy and advanced/metastatic GD2-positive osteosarcoma after progression on 1st line of chemotherapy.

All patients will receive therapy until disease progression (a total of 6 courses of immunotherapy).

The primary objective of the study is to determine the efficacy and safety of dinutuximab beta with investigator's choice of chemotherapy.

Detailed Description

Data from 40 patients are planned to be included in the study to randomize approximately 10 patients.

This study involves patients with advanced/metastatic GD2-positive rhabdomyosarcoma after progression on 1st line of chemotherapy, advanced/metastatic GD2-positive Ewing sarcoma after progression on 1st line of chemotherapy and advanced/metastatic GD2-positive osteosarcoma after progression on 1st line of chemotherapy.

6 cycles of treatment with dinutuximab beta are provided in combination with 6-8 cycles of chemotherapy during the induction therapy phase. Switching from one chemotherapy regimen to another is not allowed. Dinutuximab beta should be administered as a slow intravenous infusion through a separate catheter using an infusion pump.

All patients will receive therapy until disease progression (a total of 6 courses of immunotherapy).

Treatment response will be assessed by the investigator after 2, 4 cycles of treatment and at the end of the reinduction therapy period (i.e., after 6 cycles of dinutuximab beta treatment and 6 - 8 cycles of polychemotherapy). Treatment response will be assessed by tumor response according to the criteria for response assessment in the treatment of solid tumors (RECIST 1.1).

After discontinuation of therapy, all patients will be followed up for 6 months. All patients should be followed up to assess survival unless consent is withdrawn. Long-term follow-up/survival assessment visits will be performed monthly until death, withdrawal of consent, or study termination, whichever occurs first.

Conditions

Bone Sarcoma; Embryonal Rhabdomyosarcoma; Alveolar Rhabdomyosarcoma

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

Generalized / metastatic GD2-positive rhabdomyosarcoma

Generalized / metastatic GD2-positive rhabdomyosarcoma after progression on 1st line of chemotherapy.

Chemotherapy options:

• CARBO(CARBOPLATIN) + ETO(ETOPOSIDE), IFO(IFOSFAMIDE) + ETO(ETOPOSIDE), CARBO(CARBOPLATIN) + IFO(IFOSFAMIDE) (rhabdomyosarcoma)

+ 6 consecutive cycles of dinutuximab beta immunotherapy

Group Type: EXPERIMENTAL

dinutuximab beta

Intervention Type: DRUG

Chemotherapy + Immunotherapy (dinutuximab beta)

Generalized / metastatic GD2-positive Ewing sarcoma

Generalized / metastatic GD2-positive Ewing sarcoma after progression on 1st line of chemotherapy.

• ICE (IFOSFAMIDE+CARBOPLATIN+ETOPOSIDE), TEM(TEMOZOLOMIDE+IRINOTECAN), VCT(VINCRISTINE+CYCLOPHOSPHAN+TOPOTECAN), TC(CYCLOPHOSPHAN+TOPOTECAN), TT(TEMOZOLOMIDE+TOPOTECAN), GEM/TAX(GEMCITABINE+DOCETAXEL) (Ewing's sarcoma)

+ 6 consecutive cycles of dinutuximab beta immunotherapy

Group Type: EXPERIMENTAL

dinutuximab beta

Intervention Type: DRUG

Chemotherapy + Immunotherapy (dinutuximab beta)

Generalized / metastatic GD2-positive osteosarcoma

Generalized / metastatic GD2-positive osteosarcoma after progression on 1st line of chemotherapy.

• ICE(IFOSFAMIDE+CARBOPLATIN+ETOPOSIDE), IE (IFOSFAMIDE+ETOPOSIDE), CARBOPLATIN+ ETOPOSIDE, Аi(DOXORUBICIN+IFOSFAMIDE), IFO(IFOSFAMIDE), GEM/TAX(GEMCITABINE+DOCETAXEL) (osteosarcoma)

+ 6 consecutive cycles of dinutuximab beta immunotherapy

Group Type: EXPERIMENTAL

dinutuximab beta

Intervention Type: DRUG

Chemotherapy + Immunotherapy (dinutuximab beta)

Interventions

dinutuximab beta

Chemotherapy + Immunotherapy (dinutuximab beta)

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Signed written informed consent form;

2. Age under 18 years of age;

3. Histologically confirmed GD2-positive osteogenic sarcoma, Ewing's sarcoma, soft tissue and undifferentiated sarcomas;

4. Prior to study enrollment, patients must have been treated with one or more lines of adequate chemotherapy and must have relapsed on this therapy or have refractoriness to it;

5. General satisfactory condition of the patient (Lansky scale activity 80-100% (children under 16 years of age), Karnofsky scale 80-100% (children over 16 years of age); ECOG - 0-1);

6. Sufficient cardiopulmonary reserves of the patient's organism (ECG (ELECTROCARDIOGRAPHY) data within normal limits, ventricular ejection fraction > 75% of the upper limit of normal;

7. Adequate liver function (ALT (ALANINE AMINOTRANSFERASE) ≤ 2.5 * VGN, AST (ASPARTATE AMINOTRANSFERASE) ≤ 2.5 * VGN), kidney (creatinine <1.5 * VGN), red bone marrow (granulocytes> 2.0 * 109/L, platelets> 150 * 109/L).

Six months later, two additional criteria were formulated:

8. Life expectancy at the time of initiation of therapy within the framework of the study is not less than 12 months

9. Oligometastasis disease (presence of 1 to 5 distant metastatic foci) at restaging at the time of the decision to include the patient in the study;

Exclusion Criteria

1. Withdrawal of consent by the patient or his/her parent/guardian.

2. Exclusion of the patient by the investigator for safety or ethical reasons.

• Maximum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

N.N. Petrov National Medical Research Center of Oncology

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Svetlana Kulyova, MD, Phd

Role: PRINCIPAL_INVESTIGATOR

Head of Children's Oncology Department

Locations

Kulyova Svetlana

Saint Petersburg, , Russia

Site Status: RECRUITING

Countries

Russia

Central Contacts

Svetlana Kulyova, MD, Phd

Role: CONTACT

Kulevadoc@yandex.ru

+78124399555 ext. +79213357588

Facility Contacts

Svetlana Kulyova, MD, PhD

Role: primary

Kulevadoc@yandex.ru

+781243995553301

Svetlana Kulyova, MD, PhD

Role: backup

Kulevadoc@yandex.ru

+79213357588

Other Identifiers

821052021

Identifier Type: -

Identifier Source: org_study_id