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OncoMatch/Clinical Trials/NCT06719700

Concurrent Chemoradiotherapy Combined With Toripalimab and Surufatinib in the Treatment of Limited-Stage Small Cell Lung Cancer

Is NCT06719700 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies multiple treatments including Chemotherapy and Immunotherapy for toripalimab.

Phase 2RecruitingSun Yat-sen UniversityNCT06719700Data as of Jun 2026Location: China

Treatment: Chemotherapy · Immunotherapy · Angio-immuno kinase inhibitor · Consolidation Therapy with Toripalimab and SurufatinibBased on the preclinical rationale for combining surufatinib with immunotherapy, and the clinical efficacy observed with surufatinib in extensive-stage small cell lung cancer (ES-SCLC), the investigators hypothesize that incorporating surufatinib into the ADRIATIC regimen could further enhance survival in LS-SCLC. To evaluate this approach, the investigators plan to conduct a single-arm Phase II study to explore the safety and efficacy of concurrent chemoradiotherapy combined with toripalimab and surufatinib in treating LS-SCLC.

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Extracted eligibility criteria

Treatments studied

Targeted therapy

Consolidation Therapy with Toripalimab and Surufatinib

Other

ChemotherapyImmunotherapyAngio-immuno kinase inhibitor

Cancer type

Small Cell Lung Cancer

Disease stage

Required: Stage I, II, III

Performance status

WHO 0–1

Demographics

Ages ≤ 75

Prior therapy

Cannot have received: anti-PD-1 therapy

Previous Anti-PD-1/PD-L1 Therapy: Prior use of any anti-PD-1 or anti-PD-L1 antibodies.

Lab requirements

Blood counts

Absolute neutrophil count ≥1.5 × 10⁹/L. Platelet count ≥100 × 10⁹/L. Hemoglobin ≥9.0 g/dL.

Kidney function

Calculated creatinine clearance ≥50 mL/min using the Cockcroft-Gault formula.

Liver function

Serum bilirubin ≤1.5 × ULN. AST and ALT ≤2.5 × ULN.

Cardiac function

QTc interval (corrected by Bazett's formula) ≤470 ms, calculated from three ECG measurements.

Pulmonary Function: FEV1 ≥800 mL. Absolute neutrophil count ≥1.5 × 10⁹/L. Platelet count ≥100 × 10⁹/L. Hemoglobin ≥9.0 g/dL. Renal Function: Calculated creatinine clearance ≥50 mL/min using the Cockcroft-Gault formula. Serum bilirubin ≤1.5 × upper limit of normal (ULN). AST and ALT ≤2.5 × ULN. QTc interval (corrected by Bazett's formula) >470 ms, calculated from three ECG measurements [excluded].

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

Frequently asked questions

Is NCT06719700 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior anti-PD-1 therapy disqualifies patients from enrollment.

What disease stage is eligible?

Stage I or II or III is required.

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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