NCT06576973

Brief Summary

Esophageal cancer is a prevalent digestive tract tumor, with around 400,000 new cases and 300,000 deaths globally each year. In the past few decades, surgery, radiotherapy, chemotherapy and other treatments were continuously improved, however, the mortality of esophageal squamous cell carcinoma (ESCC) patients was not significantly decreased. For patients with locally advanced esophageal cancer, direct surgery is not effective. It is difficult to achieve radical resection by surgery merely, and even if many patients receive surgery, they may eventually have tumor recurrence and poor survival rate. Therefore, it is necessary to explore effective perioperative neoadjuvant treatment to reduce the risk of postoperative recurrence and improve the postoperative survival rate of patients. According to the reports, the expression of PD-L1 in esophageal cancer was about 41.4%. Therefore, PD-1/ PD-L1 immunocheckpoint inhibitor may become a new method for the treatment of ESCC. Preliminary clinical results showed that immunotherapy combined with chemoradiotherapy provided a synergies antitumor effect. The results of the Phase 1b trial evaluating adbelimumab monotherapy as a neoadjuvant treatment for locally advanced resectable ESCC demonstrated that patients receiving two cycles of neoadjuvant sequential surgery exhibited favorable safety profiles, with no adverse reactions of grade 3 or higher. The trial reported a major pathological response (MPR) rate of 24%, a pathological complete response (pCR) rate of 8%, a 2-year overall survival (OS) rate of 92%, and a 2-year recurrence-free survival (RFS) rate of 100%. The effectiveness of combining adbelizumab with chemotherapy and targeted therapy for locally advanced esophageal cancer is uncertain. This study aims to assess the efficacy and safety of using adbelizumab with chemotherapy and apatinib as neoadjuvant therapy for resectable ESCC.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
35

participants targeted

Target at P25-P50 for phase_2

Timeline
68mo left

Started Aug 2024

Longer than P75 for phase_2

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress24%
Aug 2024Dec 2031

Study Start

First participant enrolled

August 8, 2024

Completed
17 days until next milestone

First Submitted

Initial submission to the registry

August 25, 2024

Completed
4 days until next milestone

First Posted

Study publicly available on registry

August 29, 2024

Completed
2.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2026

Expected
5 years until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2031

Last Updated

December 2, 2025

Status Verified

November 1, 2025

Enrollment Period

2.3 years

First QC Date

August 25, 2024

Last Update Submit

November 24, 2025

Conditions

Keywords

AdbelimumabChemotherapyApatinibEsophageal Squamous Cell CarcinomaNeoadjuvant Treatment

Outcome Measures

Primary Outcomes (1)

  • Pathological Complete Response (PCR)

    The pCR will be defined as the proportion of participants with absence of residual tumor in the resected primary tumor and all resected lymph nodes after completion of neoadjuvant treatment.

    1 month after surgery

Secondary Outcomes (6)

  • Major Pathological Response (MPR)

    1 month after surgery

  • Objective Response Rate (ORR)

    before surgery

  • The changes in the peripheral blood immunoprofile and tumor tissue sample among non-PCR (NPCR) and PCR patients

    3 months after surgery

  • 2-year and 5-year overall survival

    2-year and 5-year after enrolled

  • Incidence of Treatment-related Adverse Events

    1 month after surgery

  • +1 more secondary outcomes

Study Arms (1)

Adbelimumab, chemotherapy and apatinib

EXPERIMENTAL

Preoperative neoadjuvant therapy for 4 cycles. Radical surgery is performed 4-6 weeks after the last dose. Postoperative radiotherapy is determined according to the clinical situation and pathological stage of the patient. Adbelimumab can be aintained for a maximum of 1 year. During the study, patients were be followed until disease progression, withdrawal of informed consent, loss of follow-up, or death.

Drug: Adbelimumab, Albumin paclitaxel, Carboplatin, ApatinibProcedure: EsophagectomyOther: Collecting samples from participant

Interventions

Adbelimumab 1200mg Day 1; Albumin paclitaxel 260mg/m2, Day 1; carboplatin AUC=5, Day 1; Apatinib 250mg Po Day 2-4. Preoperative neoadjuvant therapy for 4 cycles, one cycle every 21 days.

Also known as: Esophagectomy
Adbelimumab, chemotherapy and apatinib
EsophagectomyPROCEDURE

Prior to each surgical procedure, the department engaged in comprehensive discussions and deliberations to ascertain and establish the most suitable course of action. Minimally invasive IvorLewis (intrathoracic anastomosis) or McKeown (neck anastomosis) esophagectomy, including two field extensive lymphadenectomies, was performed according to the tumor location. The resection length should be at least 5cm from the tumor origin according to prechemotherapy by endoscopy. The surgeries will be performed by surgeons with rich experience. Minimally invasive esophagectomy, can be performed using the da Vinci surgical robot, thoracoscope, or laparoscope, or by using an open approach, as judged appropriate by the surgeon.

Adbelimumab, chemotherapy and apatinib

Blood, Tumour will be Collected from participant. Fate of sample is Destruction after use. 20 ml of peripheral blood was collected the day before each of the immunotherapy sessions and after surgery. Tumour sample will be collected before neoadjuvant therapy and after surgery.

Adbelimumab, chemotherapy and apatinib

Eligibility Criteria

Age18 Years - 75 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Signed informed consent.
  • Patients age 18 to 75 years old.
  • Primary resectable, histologically confirmed esophageal squamous cell cancer.
  • Esophageal squamous cell carcinoma the clinical stage was II-IVA (according to AJCC TNM stage, 8th edition).
  • ECOG PS 0-1.
  • No distant metastasis, the diseases could be resectable assessed by thoracic oncologist.

You may not qualify if:

  • With significant cardiovascular disease.
  • Current treatment with anti-viral therapy or HBV.
  • Female patients who are pregnant or lactating.
  • History of malignancy within 5 years prior to screening.
  • Active or history of autoimmune disease or immune deficiency.
  • Signs of distant metastases.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

2nd Affiliated Hospital, School of Medicine, Zhejiang University

Hangzhou, China, 310009, China

RECRUITING

MeSH Terms

Conditions

Esophageal Squamous Cell Carcinoma

Interventions

CarboplatinapatinibEsophagectomy

Condition Hierarchy (Ancestors)

Carcinoma, Squamous CellCarcinomaNeoplasms, Glandular and EpithelialNeoplasms by Histologic TypeNeoplasmsNeoplasms, Squamous CellEsophageal NeoplasmsGastrointestinal NeoplasmsDigestive System NeoplasmsNeoplasms by SiteHead and Neck NeoplasmsDigestive System DiseasesEsophageal DiseasesGastrointestinal Diseases

Intervention Hierarchy (Ancestors)

Coordination ComplexesOrganic ChemicalsDigestive System Surgical ProceduresSurgical Procedures, Operative

Study Officials

  • Wang

    2nd Affiliated Hospital, School of Medicine, Zhejiang University

    STUDY CHAIR

Central Study Contacts

Study Design

Study Type
interventional
Phase
phase 2
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 25, 2024

First Posted

August 29, 2024

Study Start

August 8, 2024

Primary Completion (Estimated)

December 1, 2026

Study Completion (Estimated)

December 1, 2031

Last Updated

December 2, 2025

Record last verified: 2025-11

Locations