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OncoMatch/Clinical Trials/NCT07086469

Surufatinib in Combination With Neoadjuvant Chemo-immunotherapy and Concurrent Chemoradiotherapy for Patients With Unresectable Locally Advanced Esophageal Squamous Cell Carcinoma

Is NCT07086469 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies multiple treatments including Neoadjuvant immunochemotherapy and Surufatinib Administration for toripalimab.

Phase 2RecruitingSun Yat-sen UniversityNCT07086469Data as of Jun 2026Location: China

Treatment: Neoadjuvant immunochemotherapy · Surufatinib Administration · Concurrent ChemotherapyThe combination of surufatinib with neoadjuvant chemo-immunotherapy and definitive concurrent chemoradiotherapy represents a promising new therapeutic strategy that may further improve the prognosis of patients with unresectable locally advanced esophageal squamous cell carcinoma (ESCC). Therefore, we propose to conduct a prospective, single-arm, phase II clinical trial to evaluate the efficacy and safety of this regimen in patients with unresectable, locally advanced ESCC.

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Extracted eligibility criteria

Treatments studied

Other

Neoadjuvant immunochemotherapySurufatinib AdministrationConcurrent Chemotherapy

Cancer type

Esophageal Carcinoma

Disease stage

Required: Stage M1 (LIMITED TO SUPRACLAVICULAR LYMPH NODE METASTASIS)

Locally advanced, unresectable esophageal cancer...staged as T2-4, N0-3, M0-1 (M1 limited to supraclavicular lymph node metastasis).

Performance status

ECOG 0–1(Restricted strenuous activity)

Demographics

Ages ≤ 80

Prior therapy

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

Cannot have received: chemotherapy

Cannot have received: radiotherapy

Cannot have received: surgery

Cannot have received: targeted therapy

Cannot have received: immunotherapy

Lab requirements

Blood counts

anc ≥ 1.5 × 10⁹/l; platelet count ≥ 100 × 10⁹/l; hemoglobin ≥ 90 g/l

Kidney function

creatinine clearance ≥ 50 ml/min calculated by the cockcroft-gault formula

Liver function

total bilirubin ≤ 1.5 × uln; alt and ast ≤ 2.5 × uln

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

Frequently asked questions

Is NCT07086469 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 M1 (LIMITED TO SUPRACLAVICULAR LYMPH NODE METASTASIS) is required.

Is there an age limit?

Yes. Patients must be 80 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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