A Clinical Study of Sintilimab as Adjuvant Therapy in Node-positive ESCC

NCT ID: NCT06190639

Last Updated: 2024-01-05

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 31 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-10-25
• Study Completion Date: 2027-12-31

Brief Summary

The goal of this clinical trial is to evaluate the efficacy and safety of sintilimab as adjuvant therapy in node-positive esophageal squamous cell carcinoma after radical surgery without neoadjuvant therapy. The main question it aims to answer is:

• Efficacy of sintilimab as adjuvant therapy Participants will receive sintilimab 200 mg once on day 1, every 21 days(Q3W).

Conditions

Esophageal Squamous Cell Carcinoma

Study Design

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

Study Groups

Experimental group

Group Type: EXPERIMENTAL

sintilimab

Intervention Type: DRUG

200 mg once on day 1, every 21 days

Interventions

sintilimab

200 mg once on day 1, every 21 days

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Signed an Informed Consent Form

2. Participant type and target disease characteristics:

• ECOG PS 0-1
• Histologically confirmed T1-3N+M0 thoracic esophageal squamous cell cancer (AJCC 8th)
• can tolerate radical resection of esophageal cancer
• Resection must be performed within 4-12 weeks prior to enrollment
• All participants must be confirmed disease-free by physical and imaging examinations within 4 weeks prior to enrollment. Imaging examinations must include CT/MRI scans of the neck, chest and abdomen.
• All baseline laboratory tests will be evaluated as required and results should be available within 28 days prior to enrollment. Laboratory test values must be selected according to the following criteria (CTCAE V5.0):

1. WBC ≥2000/μL;

2. Neutrophils ≥1500/μL;

3. Platelets ≥100 x 103/μL;

4. Hemoglobin ≥9.0 g/dL;

5. Creatinine: Serum creatinine ≤1.5 x above normal (ULN) or creatinine removal rate > 50mL/ min (Cockcroft/Gault formula);

6. AST ≤3 x ULN;

7. ALT ≤3 x ULN;

8. Total bilirubin ≤1.5 x ULN (except for subjects with Gilbert syndrome, where total bilirubin must be < 3 x ULN);

3. Age and fertility status:

• Age ≥18 years old
• Women of child bearing potential (WOCBP) must have a negative serum or urine pregnancy test (minimum sensitivity of HCG is 25 IU/L or equivalent) within 24 hours before starting study treatment.
• Women must be non-breastfeeding

Exclusion Criteria

1. Target disease

• The presence of locally advanced unresectable (regardless of stage) or metastatic disease.
• Cervical and abdominal esophageal tumors.

2. Medical history and concurrent diseases

• Complete resection followed by treatment for the removed esophageal cancer (e.g., chemotherapy, targeted drugs, radiation, or biotherapy).
• Participants with ≥ grade 2 peripheral neuropathy
• Participants with active, known, or suspected autoimmune diseases. Participants with type I diabetes, hypothyroidism requiring only hormone replacement therapy, skin conditions that do not require systemic treatment (such as vitiligo, psoriasis, or hair loss), or conditions that are not expected to recur without external irritants, may be enrolled.
• Glucocorticoids are required for 14 days prior to treatment (daily>10 mg equivalent dose of prednisone) or other immunosuppressive drugs for systemic treatment.

If there is no active autoimmune disease, inhaled or topical steroid hormones are permitted, and daily>10 mg prednisone equivalent dose of adrenal hormone replacement therapy.

• A known history of testing positive for human immunodeficiency virus (HIV) or a known history of acquired immunodeficiency syndrome (AIDS)
• Participants with a serious or uncontrolled medical condition.
• Radiotherapy, chemotherapy, immunotherapy, esophagectomy, esophagus-gastric junction, and gastric surgery were performed before the trial.
• Participants with severe cardiovascular or pulmonary disease, interstitial pneumonia, or a history of prior interstitial pneumonia.
• Active malignancy within the last 3 years, other than locally curable cancers that have apparently been cured, such as basal or squamous cell skin cancer, superficial bladder cancer, or carcinoma in situ of the prostate, cervix, or breast.
• Participants with a serious or uncontrolled medical condition

3. Physical and laboratory examination

• Participants were found to have active hepatitis B (Hepatitis B surface antigen [HBsAg] positive or hepatitis C virus (HCV) positive (HCV RNA positive) Sex). Participants with prior HBV infection or recovered HBV infection (defined as having hepatitis B core antibodies [HBcAb] and no HBsAg) were eligible. HBV DNA must be obtained from these patients before treatment. Participants who are HBV carriers or require antiviral therapy are not eligible to participate. Participants who were positive for HCV antibodies were eligible only if the PCR for HCV RNA was negative.

4. Allergies and adverse drug reactions

• History of allergy or hypersensitivity to study drug ingredients.
• A history of severe hypersensitivity to any monoclonal antibody.

• Participants who do not understand or may not comply with the requirements of the trial
• Participants had an active infection requiring systemic treatment in the 28 days prior to first dosing
• Some obvious diseases that the researchers believe should be excluded from this study

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

Sponsors

Zhejiang Cancer Hospital

OTHER

Sponsor Role: lead

Responsible Party

Changchun Wang

Clinical Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Zhejiang Cancer Hospital

Hangzhou, Zhejiang, China

Site Status: RECRUITING

Countries

China

Central Contacts

Changchun Wang, MD

Role: CONTACT

wangcc@zjcc.org.cn

13606520363

Facility Contacts

Changchun Wang, MD

Role: primary

Other Identifiers

IRB-2023-768

Identifier Type: -

Identifier Source: org_study_id