RecruitingPhase 1Phase 2NCT04433221

Combination Immunotherapy Targeting Sarcomas

Safety and Efficacy Evaluation of a Combination Immunotherapy Targeting Sarcomas

Sponsor

Shenzhen Geno-Immune Medical Institute

Enrollment

20 participants

Start Date

Jul 1, 2026

Study Type

INTERVENTIONAL

Conditions

Sarcoma Ewing Sarcoma Osteoid Sarcoma

Summary

The aim of this clinical trial is to assess the feasibility, safety and efficacy of a combination low dose chemotherapy and immunotherapy in patients who have sarcoma that is relapsed or late staged. Another goal of the study is to assess the safety and efficacy of the therapy that combines multiple CAR T cells followed by sarcoma vaccines.

Eligibility

Min Age: 1 YearMax Age: 75 Years

Inclusion Criteria13

Stage Ⅲ，Ⅳ sarcoma patients or recurrent sarcoma patients;
Age: ≥ 6 months and ≤80 years of age at the time of enrollment;
At least 2 weeks since the last standard chemotherapy or radiotherapy and immunosuppressive therapy such as steroid hormone before enrollment;
Side effects of chemotherapy have been well managed;
Confirmed malignant cell expression of CART target antigens by IHC or flow
Karnofsky /jansky score of 50% or greater;
Expected survival > 8 weeks;
ANC≥ 1×10\^6/L，PLT ≥ 1×10\^8/L;
Pulse oximetry of≥90% on room air；
Adequate hepatic function, defined as aspartate aminotransferase(AST)< 5 times upper limit of normal(ULN),serum bilirubin < 3 times ULN;
Adequate renal function, defined as serum creatinine less than 2 times ULN, if serum creatinine more than 1.5 times ULN, creatinine clearance rate test is needed;
Patients must have sufficient autologous CART cells at does greater than 0.5x10\^6 cells/kg body weight;
Sign an informed consent and assent.

Exclusion Criteria16

The disease is progressing rapidly;
The patient is receiving therapy of other new drugs and under evaluation;
Evidence of tumor potentially causing airway obstruction;
Epilepsy history or other CNS diseases;
Patients who need immunosuppressive drugs;
History of long QT syndrome or severe heart diseases;
Uncontrolled active infection;
Active hepatitis B virus, hepatitis C virus or HIV infection;
Receiving systemic corticosteroid 2 weeks before enrollment except for inhaled steroids;
Previous treatment with any gene therapy;
Creatinine>2.5mg/dl or ALT/AST>3 times normal or bilirubin>2.0 mg/dl;
Patients who have other uncontrolled diseases such as obstruction of lung function would preclude participation as outlined;
Pregnant or lactating women;
Patients previously experienced toxicity from cyclophosphamide and doxorubicin;
Patients who have CNS sarcoma;
In condition that may bring risks to subjects or interference to clinical trials.