OncoMatch

OncoMatch/Clinical Trials/NCT05507411

Watch and Wait for NeoAdjuvant Concurrent Radiochemotherapy Combined With Camrelizumab in Patients With Resectable ESCC

Is NCT05507411 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments including Neoadjuvant Chemotherapy and Immunotherapy for esophageal squamous cell carcinoma.

Phase 2RecruitingZhejiang Cancer HospitalNCT05507411Data as of May 2026

Treatment: Neoadjuvant Chemotherapy · ImmunotherapyTo observe the 1-year disease-free survival rate (1-year PFS) of patients with resectable esophageal squamous cell carcinoma who received neoadjuvant chemoradiotherapy combined with camrelizumab and achieved clinical complete remission with watchful waiting strategy.

Check if I qualify

Extracted eligibility criteria

Cancer type

Esophageal Carcinoma

Biomarker criteria

Required: PD-L1 (CD274) any tested (testing required; no eligibility threshold specified)

Disease stage

Required: Stage CT2-4ANANYM0, CT1-3N+M0

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

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

Cannot have received: chest radiotherapy

Received chest radiotherapy ... prior to the start of the trial

Cannot have received: chemotherapy

Received ... chemotherapy ... prior to the start of the trial

Cannot have received: immunotherapy

Received ... immunotherapy ... prior to the start of the trial

Cannot have received: surgery of the esophagus, esophagus and gastric junction, or stomach

Received ... surgery of the esophagus, esophagus and gastric junction, or stomach prior to the start of the trial

Lab requirements

Blood counts

WBC ≥ 2000/μL; Neutrophils ≥ 1500/μL; Platelets ≥ 100x10^3/μL; Hemoglobin ≥ 9.0 g/dL

Kidney function

Serum creatinine ≤1.5 x ULN or calculated creatinine clearance (CrCl) ≥ 50 mL/min (using Cockcroft-Gault formula)

Liver function

AST ≤ 3.0 x ULN; ALT ≤ 3.0 x ULN; Total bilirubin ≤ 1.5 x ULN (except for Gilbert syndrome participants, who had total bilirubin < 3.0 x ULN)

Laboratory screening values must meet the following criteria (using CTCAE 4th edition): i) WBC < 2000/μL; ii) Neutrophils < 1500/μL; iii) Platelets < 100x103/μL; iv) Hemoglobin < 9.0 g/dL; v) Serum creatinine <1.5 x ULN or calculated creatinine clearance (CrCl) < 50 mL/min (using Cockcroft-Gault formula); vi) AST >3.0 x ULN; vii) ALT > 3.0 x ULN; viii) Total bilirubin >1.5 x ULN (except for Gilbert syndrome participants, who had total bilirubin < 3.0 x ULN)

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

Could you qualify for this trial?

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

Check if I qualify