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OncoMatch/Clinical Trials/NCT07657325

Study on MRD Prediction of Efficacy of Toripalimab in the Treatment of High-risk Recurrent Renal Carcinoma

Is NCT07657325 recruiting? Yes, currently enrolling (Sep 2026). Studying Toripalimab for renal cell carcinoma (rcc).

RecruitingTianjin Medical University Second HospitalNCT07657325Data as of Sep 2026Location: China

Treatment: Toripalimab

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Extracted eligibility criteria

Treatments studied

Immunotherapy

Toripalimab

Cancer type

Renal Cell Carcinoma

Disease stage

Required: Stage PT4, ANY GR. N0, M0, PT ANY STAGE, ANY GR., N+, M0, M1 NED (other)

High risk or M1 NED renal cell carcinoma as defined by the following pathological tumor-node-metastasis and Fuhrman grading status.

Performance status

ECOG 0–1(Restricted strenuous activity)

ECOG Performance Status (ECOG PS) of 0 or 1

Prior therapy

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

Lab requirements

Blood counts

normal bone marrow reserve function; Absolute neutrophil count (ANC)≥1500/µL, Platelets≥100,000/µL, Hemoglobin ≥5.6 mmol/L (9g/dL)

Kidney function

Normal renal function or serum creatinine ≤1.5 mg/dL and/or creatinine clearance ≥30 mL/min for participants with creatinine levels >1.5×institutional ULN

Liver function

Normal liver function or Total bilirubin ≤1.5xULN, or direct bilirubin≤ULN for participants with total bilirubin levels >1.5×ULN; AST (SGOT) and ALT (SGPT) ≤2.5×ULN

Vital organ function meets the following requirements (excluding use of any blood components and cell growth factors within 14 days) : normal bone marrow reserve function; Absolute neutrophil count (ANC)≥1500/µL, Platelets≥100 000/µL, Hemoglobin ≥5.6 mmol/L (9g/dL); Normal renal function or serum creatinine ≤1.5 mg/d and/or creatinine clearance ≥30 mL/min for participants with creatinine levels >1.5×institutional ULN; Normal liver function or Total bilirubin ≤1.5xULN, or direct bilirubin≤ULN for participants with total bilirubin levels >1.5×ULN; AST (SGOT) and ALT (SGPT) ≤2.5×ULN; International normalized ratio (INR) or prothrombin time (PT) ≤1.5×ULN.

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

Frequently asked questions

Is NCT07657325 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.

What disease stage is eligible?

Stage PT4, ANY GR. N0, M0 or PT ANY STAGE, ANY GR., N+, M0 or M1 NED is required.

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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