Overview

Candonilimab (AK104) Plus Preoperative Chemotherapy for Locally Advanced Esophageal Squamous Cell Carcinoma (ESCC)

Status:
Not yet recruiting
Trial end date:
2026-08-01
Target enrollment:
0
Participant gender:
All
Summary
This is a prospective, single-arm, open-label,multi-center, phase II study, aiming to evaluate the efficacy and safety of AK104 combined with preoperative chemotherapy in patients with locally advanced ESCC.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
The First Affiliated Hospital of Zhengzhou University
Treatments:
Carboplatin
Paclitaxel
Criteria
Inclusion Criteria:

1. Voluntarily signing a written informed consent form;

2. Males or females aged ≥ 18 to ≤ 70 years;

3. ECOG score 0-1;

4. Pathologically diagnosed thoracic esophageal squamous cell carcinoma;

5. No distant metastasis after imaging examination, and esophageal cancer can be resected
or potentially resectable with stage cT1b-cT2N+M0 or cT3-cT4a anyN M0 or cT2N0M0
high-risk (lymphovascular invasion or tumor ≥3 cm or hypo-differentiation) (AJCC 8th
edition cTNM stage);

6. Not received prior antitumor therapy (surgery, radiotherapy, chemotherapy,
immunotherapy, etc. for esophageal cancer);

7. Life expectancy is greater than 6 months;

8. At least one measurable tumor lesion per RECIST v1.1;

9. Major organ functions are adequate;

Exclusion Criteria:

1. Patient has received previous antitumor therapy (chemotherapy, radiation, surgery or
immunotherapy);

2. Cervical or thoracic esophageal cancer is < 5 cm from the cricopharyngeal muscle;

3. Patients are or are expected to be at significant risk of esophageal perforation,
fistula, and major bleeding;

4. Imaging during the screening period showed that the tumor surrounded or invaded
important blood vessels or organs (such as the heart and pericardium, trachea, aorta,
superior vena cava, etc.) or there was obvious necrosis or cavity, and the
investigator determined that entering the study would cause bleeding risk;
participants at risk of developing oesophageal or oesophageal fistula;

5. Patients with a history of other malignant diseases in the last 5 years,unless
complete resolution or no additional treatment is required (exceptions include, but
are not limited to, basal or squamous cell skin cancer, superficial bladder cancer or
prostate, cervix, or breast carcinoma in situ);

6. Pregnant or nursing women;

7. Patients with known or suspected active autoimmune disease;

8. Patients with a history of myocarditis, cardiomyopathy, malignant arrhythmias;

9. Other patients are not eligible for enrollment assessed by investigators;