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Efficacy and safety of doxorubicin liposomal and adebrelimab in the treatment of osteosarcoma failed standard treatment: a multicenter, interventional clinical study

Efficacy and safety of doxorubicin liposomal and adebrelimab in the treatment of osteosarcoma failed standard treatment: a multicenter, interventional clinical study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600115969
Enrollment
Unknown
Registered
2026-01-04
Start date
2026-01-07
Completion date
Unknown
Last updated
2026-01-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osteosarcoma

Interventions

Experimental group:All eligible subjects will receive up to 6 cycles of liposomal doxorubicin plus atezolizumab combination therapy under the guidance of the MDT team. atezolizumab will be maintained

Sponsors

Shanghai Sixth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Osteosarcoma confirmed by histology, with SSS staging of inoperable stage II and metastatic stage III; 2. No other concurrent tumor types; 3. Have received at least first-line systemic treatment in the past and are resistant to drugs; 4. Not previously treated with PD-1 or PD-L1; The cumulative dosage of doxorubicin is =50%; 6. ECOG PS 1-2; 7. Expected lifespan>3 months; 8. 12-60 years old; 9. At least one measurable lesion (RECIST 1.1); 10. Adequate organ function.

Exclusion criteria

Exclusion criteria: 1. Simultaneously suffering from other types of malignant tumors. 2. Cardiac dysfunction or arrhythmia. 3. Uncontrollable complications, such as diabetes. 4. Coagulation disorders. 5. Urinary protein >=++. 6. Chest or peritoneal effusion that requires surgical treatment. 7. Unable to obtain an appropriate amount of tumor tissue through biopsy. 8. Merge other infections or wounds. 9. There are other serious physical or mental illnesses or laboratory abnormalities that may increase the risk of participating in the study, or interfere with the study results, as well as patients deemed unsuitable by the researchers to participate in this study. 10. Allergic to anthracycline drugs or experiencing hyperprogression reactions during previous treatment with immune checkpoint inhibitors. 11. Vasodilatory osteosarcoma

Design outcomes

Primary

MeasureTime frame
Objective Response Rate;

Secondary

MeasureTime frame
Progression-free survival;Overall survival;Adverse event;

Countries

China

Contacts

Public ContactYang Qingcheng, Yonggang Wang

Shanghai Sixth People's Hospital

sirui666@163.com+86 139 1732 1736

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026