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Changes in Tumor Tissue and Serum Biomarkers Before and After Cetuximab Combined With Preoperative Radiotherapy in Locally Advanced Thoracic Esophageal Squamous Cell Carcinoma

Changes in Tumor Tissue and Serum Biomarkers Before and After Cetuximab Combined With Preoperative Radiotherapy in Locally Advanced Middle or Lower Thoracic Esophageal Squamous Cell Carcinoma

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02123381
Enrollment
100
Registered
2014-04-25
Start date
2014-04-30
Completion date
2020-07-31
Last updated
2020-03-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Locally Advanced Thoracic Middle-lower Segment Esophageal Squamous Cell Carcinoma

Keywords

tumor tissue and serum biomarkers, cetuximab, preoperative radiotherapy, esophageal squamous cell carcinoma

Brief summary

This study aim to investigate Changes in tumor tissue and serum biomarkers before and after cetuximab combined with preoperative radiotherapy in locally advanced thoracic middle-lower segment esophageal squamous cell carcinoma.We want to find one or more effective biomarkers to predict and evaluate the patients who will be benefit from cetuximab combined with preoperative radiotherapy.

Interventions

Patients receive intensity modulated radiation therapy(IMRT) or image-guided radiation therapy(IGRT)from week 1 to week 4,once a day, 5 times per week. Radiotherapy dose:95% gross tumor volume(GTV-T) 40Gy/20f,GTV-N 40Gy/20f,CTV-T 40Gy/20f,CTV-N 40Gy/20f.

DRUGcetuximab

400mg/m2/week, 2 hours,iv,at week 1;250mg/m2/week,1hour,iv,at week 2-4

Sponsors

Daping Hospital and the Research Institute of Surgery of the Third Military Medical University
CollaboratorOTHER
Affiliated Cancer Hospital & Institute of Guangzhou Medical University
CollaboratorOTHER
Southwest Hospital, China
CollaboratorOTHER
Xinqiao Hospital of Chongqing
CollaboratorOTHER
Sichuan Cancer Hospital and Research Institute
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

(1)18 to 65 years old,male or female (2)Pathologically or cytologically proven thoracic middle-lower esophageal squamous cell carcinoma; (3)clinical stage II or stage III; (4)Primary tumors can be measured; (5)Karnofsky score \>70; (6)Estimated life expectancy of at least 12 weeks; (7)reproductive age women should ensure that before entering the study period contraception; (8)Hemoglobin≥90.0g/dL,white blood cell count(WBC)≥ 4000 cells/mm³,Platelet count≥100,000 cells/mm³; (9)Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) \< 2.5 times upper limit of normal,bilirubin normal; (10)Creatinine normal OR creatinine clearance ≥ 60 mL/min; (11)Patients have good compliance to treatment and follow-up of acceptance; (12)Forced expiratory volume in one second(FEV1) ≥ 1.5 litre or ≥ 75% of the reference value; (13)Considered operable (i.e. appropriate organ functions and ability to undergo general anesthesia); (14)No severe or uncontrolled cardiovascular disease; (15)No active uncontrolled infection;

Exclusion criteria

1. Patient who have distant metastasis 2. The primary tumor or lymph node already received surgical treatment (except for biopsy); 3. Patient who received radiotherapy for primary tumor or lymph node; 4. Patient who received the the epidermal growth factor targeted therapy; 5. Patient who received chemotherapy or immunotherapy; 6. Patient who suffered from other malignant tumor; 7. Epidermal growth factor receptor(EGFR)mutation(-); 8. Patient who have taken other drug test within 1 month; 9. Pregnant woman or Lactating Women and Women in productive age who refuse to take contraception in observation period; 10. Subject with a severe allergic history or idiosyncratic; 11. Subject with severe pulmonary and cardiopathic disease history; Refuse or incapable to sign the informed consent form of participating this trial; 12. Drug abuse or alcohol addicted; 13. Subject with a Personality or psychiatric diseases, people with no legal; capacity or people with limited capacity for civil conduct;

Design outcomes

Primary

MeasureTime frameDescription
Expression of Survivin protein in Esophageal Squamous Cell Carcinoma before and after Radiotherapybefore radiotherapy and 1 months after the radiotherapySurvivin, an inhibitor of apoptosis protein, is highly expressed in most cancers and associated with radiotherapy resistance, increased tumor recurrence, and shorter patient survival.
Expression of p53 in Esophageal Squamous Cell Carcinoma before and after Radiotherapybefore radiotherapy and 1 months after the radiotherapyp53 (also known as protein 53 or tumor protein 53), is a tumor suppressor protein that in humans is encoded by the TP53 gene.p53 is important in multicellular organisms and involved in preventing cancer.
changes of serum vascular endothelial growth factor(VEGF)level before and after radiotherapybefore radiotherapy and 1 months after the radiotherapyVascular endothelial growth factor (VEGF) is a signal protein produced by cells that stimulates vasculogenesis and angiogenesis.

Secondary

MeasureTime frameDescription
local control rate(LCR)up to 3 yearsTime to locoregional failure after R0 resection
Quality of life (QOL)up to 3 yearsQuality of life (QOL) as measured by European Organization for Research and Treatment of Cancer quality of life questionnaire (EORTC QLQ-C30)
grade 3-5 adverse eventsup to 3 yearsGrade 3-5 adverse events as assessed by NCI Common Toxicity Criteria for Adverse Effects (CTCAE) v3.0,such as esophagitis、pneumonitis and hematologic toxicity
Pathological remission1 months after the end of surgery
Overall survivalup to 3 yearstime from randomization to death
PFS(progression-free survival)up to 3 yearstime from randomization to one of the following events, whichever comes first: 1. Tumor progression at any time (progression of primary tumor or local lymph nodes, appearance of new lesions) 2. Recurrence at local, regional or distant site after surgery 3. Death from any cause

Countries

China

Contacts

Primary ContactTAO LI, MD, PhD
litaoxmf@126.com86-18908178818

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026