Clinical trial

Neoadjuvant Therapy of PD-1 Blockade Combined With Chemotherapy for Locally Advanced Esophageal Carcinoma

Name
BeijingHF
Description
This prospective study aims to clarify the clinical efficacy and survival prognosis of neoadjuvant immune checkpoint inhibitor (ICI) combined with chemotherapy for esophageal cancer. It also explores predictive biomarkers and potential therapeutic targets for locally advanced esophageal cancer based on plasma metabolomics and peripheral blood immune cell clustering analysis. Each patient received 2-3 cycles of neoadjuvant immunotherapy with programmed cell death 1 (PD-1) blockade in combination with albumin paclitaxel and platinum. Exploratory analysis of plasma metabolomics combined with peripheral blood subsets of immune cells can reveal biomarkers that predict the efficacy and prognosis of patients undergoing neoadjuvant immunotherapy for locally advanced esophageal cancer, which also provide new ideas for the selection of immune adjuvants and therapeutic targets in ICIs combination therapy strategies.
Trial arms
Trial start
2020-10-29
Estimated PCD
2023-12-31
Trial end
2024-12-31
Status
Recruiting
Phase
Early phase I
Treatment
PD-1 blockade
PD-1 blockade (Sintilimab/Camrelizumab/Toripalimab/Tislelizumab), 200 mg, IV., every 3 weeks, 2-3 cycles.
Arms:
Neoadjuvant PD-1 Blockade Plus Chemotherapy
Albumin paclitaxel
Albumin paclitaxel, 300 mg/m2, IV., every 3 weeks, 2-3 cycles.
Arms:
Neoadjuvant PD-1 Blockade Plus Chemotherapy
Carboplatin/Nedaplatin
Carboplatin/Nedaplatin, area under the curve = 5, IV., every 3 weeks, 2-3 cycles.
Arms:
Neoadjuvant PD-1 Blockade Plus Chemotherapy
Size
89
Primary endpoint
Disease-free survival (DFS)
24 months
Eligibility criteria
Inclusion Criteria: 1. age ≥ 18 years and ≤89 years; 2. pathological histological examination confirmed the diagnosis of esophageal squamous cell carcinoma and esophageal adenocarcinoma; 3. clinical stage II-IVA; 4. adequate organ function; 5. no previous chemotherapy or radiotherapy; 6. voluntarily signed informed consent. Exclusion Criteria: 1. the presence of concurrent malignancies that interfere with the prognosis of esophageal cancer; 2. patients with immunodeficiency or autoimmune diseases that seriously affect the body's immune system, such as those who test positive for HIV; 3. patients undergoing systemic corticosteroid or other immunosuppressive treatments; 4. patients with a history of allergy to the components of this test drug.
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE1', 'PHASE2'], 'designInfo': {'allocation': 'NA', 'interventionModel': 'SINGLE_GROUP', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 89, 'type': 'ESTIMATED'}}
Updated at
2023-03-21

1 organization

3 products

2 indications