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OncoMatch/Clinical Trials/NCT06849986

IO Combined With AI as First-line Treatment for Patients With Soft Tissue Sarcoma(TAIS)

Is NCT06849986 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies Tislelizumab+liposomal doxorubicin+ifosfamide for soft tissue sarcomas.

Phase 2RecruitingFudan UniversityNCT06849986Data as of Jun 2026Location: China

Treatment: Tislelizumab+liposomal doxorubicin+ifosfamideThis study will enroll patients with specific subtypes of unresectable or metastatic soft tissue sarcoma, and will combine tislelizumab with the standard chemotherapy of liposomal doxorubicin and ifosfamide to initially explore the efficacy and safety.

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Extracted eligibility criteria

Treatments studied

Chemotherapy

Tislelizumab+liposomal doxorubicin+ifosfamide

Cancer type

Sarcoma

Performance status

ECOG 0–1(Restricted strenuous activity)

Demographics

Ages ≤ 75

Prior therapy

No prior treatment (treatment-naive required)
Max 0 prior lines

Cannot have received: systemic therapy for advanced soft tissue sarcoma

Exception: relapsed more than six months after adjuvant therapy with a cumulative dose of doxorubicin ≤300mg/m2

Previous treatment for advanced soft tissue sarcoma, except for those who relapsed more than six months after adjuvant therapy with a cumulative dose of doxorubicin ≤300mg/m2

Cannot have received: experimental or anti-tumor drugs

Received any experimental or anti-tumor drugs within 4 weeks prior to enrollment

Cannot have received: anti-PD-1, anti-PD-L1, anti-PD-L2, anti-CD137, or anti-CTLA-4 antibody or any other antibodies or drugs specifically targeting T-cell co-stimulation or checkpoint pathways

Previously received any anti-PD-1, anti-PD-L1, anti-PD-L2, anti-CD137, or anti-CTLA-4 antibody treatment, or any other antibodies or drugs specifically targeting T-cell co-stimulation or checkpoint pathways

Lab requirements

Blood counts

neutrophil count ≥1.5×10⁹/l, platelet count ≥90×10⁹/l, hemoglobin ≥90g/l (no blood transfusion within 14 days)

Kidney function

serum creatinine ≤1.5× uln or creatinine clearance rate ≥50ml/min

Liver function

serum total bilirubin ≤1.5 times uln; alt and ast ≤2.5× uln (≤5× uln for patients with liver metastases)

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

Frequently asked questions

Is NCT06849986 currently recruiting?

Yes, this trial is currently recruiting patients.

Can patients have received prior systemic therapy?

No. This trial requires treatment-naive patients — prior systemic therapy is an exclusion criterion.

Is there an age limit?

Yes. Patients must be 75 years or younger.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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Related pages

Sarcoma trials