Tislelizumab Combined With Chemotherapy for the Perioperative Treatment of Esophageal Squamous Carcinoma

NCT ID: NCT07019181

Last Updated: 2025-06-13

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 26 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-07-30
• Study Completion Date: 2026-12-31

Brief Summary

Evaluating the rate of pathologic complete remission in patients with squamous esophageal cancer treated perioperatively with tislelizumab in combination with chemotherapy

Conditions

Esophagus Cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Tislelizumab combined with chemotherapy

Group Type: EXPERIMENTAL

Tislelizumab

Intervention Type: DRUG

Tislelizumab, 200mg, intravenously over 30 - 60 minutes, day 1 of every 3 weeks

albumin-bound paclitaxel

Intervention Type: DRUG

albumin-bound paclitaxel 260mg/m2，day 1 of every 3 weeks

Nedaplatin

Intervention Type: DRUG

Nedaplatin 80mg/m2，day 1 of every 3 weeks

Interventions

Tislelizumab

Tislelizumab, 200mg, intravenously over 30 - 60 minutes, day 1 of every 3 weeks

Intervention Type: DRUG

albumin-bound paclitaxel

albumin-bound paclitaxel 260mg/m2，day 1 of every 3 weeks

Intervention Type: DRUG

Nedaplatin

Nedaplatin 80mg/m2，day 1 of every 3 weeks

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Subjects were enrolled in the study and signed an informed consent form.
• Male or female patients between the ages of 18 and 75.
• Patients with esophageal squamous carcinoma diagnosed by histopathology.
• According to the TNM staging system of esophageal cancer in the 8th edition of the AJCC,the disease is in the stage of cT3-4aN0M0 or cT1b-4aN+M0 (confirmed by thoracic and abdominal enhancement CT/MRI), and the lesion is located in the thoracic segment.
• ECOG score: 0-1.
• Normal functioning of major organs, i.e. meeting the following criteria.

1. Blood count (no blood transfusions, granulocyte colony-stimulating factor [G-CSF], or other medications corrected within 14 days prior to treatment); and Absolute neutrophil count (ANC) ≥1.5×109/L; hemoglobin (HB) ≥9.0 g/dL; and Platelet count (PLT) ≥ 100 x 109/L;

2. blood biochemistry Creatinine clearance ≥60 mL/min. Total bilirubin (TBIL) ≤ 1.5 x ULN. Albuminous aminotransferase (AST) or albuminous aminotransferase (ALT) levels ≤ 2.5 x ULN;

• Expected survival > 6 months.
• Female subjects of childbearing potential and male subjects with partners of childbearing potential are required to use a medically approved contraceptive method during study treatment and for at least 6 months after the last treatment.

Exclusion Criteria

• The presence of clinically uncontrolled chest that required repeated drainage or medical intervention (within 2 weeks prior to randomization) Hydrocele, pericardial hydrocele or ascites;
• Known intolerance or resistance to chemotherapy specified in the trial protocol;
• Have received any other ESCC anti-tumor therapy (e.g., targeting PD-1, PD-L1, PD-L2) Or other tumor immunotherapy, radiotherapy, targeted therapy, ablation, or other systemic or local anti-tumor therapy);
• Patients who have an active autoimmune disease or have a history of an autoimmune disease but may relapse may have a known abnormality History of body organ transplantation or allogeneic hematopoietic stem cell transplantation;
• A history of interstitial lung disease, non-infectious pneumonia, or uncontrolled systemic disease, including pulmonary fibrosis, Acute lung disease;
• There were severe chronic or active patients requiring systemic antimicrobial therapy, antifungal therapy or antiviral therapy before enrollment Infection (including tuberculosis infection, etc.);
• Have a known history of HIV infection;
• The presence of any serious or uncontrolled systemic disease, including but not limited to:

Unstable angina pectoris, congestive heart failure, New York Heart Association (NYHA) grade ≥ 2 chronic heart failure; Any arterial thrombosis, embolism, or ischemia, such as myocardial infarction, cerebrovascular accident, or transient ischemic attack, during the 6 months prior to the first dose of the study; Uncontrolled hypertension (i.e., ≥ CTC-AE level 2 hypertension after medication); active pulmonary tuberculosis; those who have a history of psychotropic substance abuse and cannot abstain or have mental disorders;

• Had other malignancies in the past 5 years (cured skin basal cell carcinoma, breast carcinoma in situ and Except primary cervical cancer);
• Had received live vaccine within 28 days prior to enrollment;
• Have participated in other therapeutic clinical trials within 4 weeks;
• And those deemed unsuitable for inclusion by the researchers.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

The First Affiliated Hospital of Xiamen University

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Central Contacts

Geng guo jun, Doctor

Role: CONTACT

ggj622@126.com

13365922380 ext. 86

Other Identifiers

SL-2024KY088-01

Identifier Type: -

Identifier Source: org_study_id