Skip to content

A randomized controlled study for Endostar and Hyperthermia Combined with chemoradiotherapy for locally advanced esophageal cancer

A randomized controlled study for Endostar and Hyperthermia Combined with chemoradiotherapy for locally advanced esophageal cancer

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900022096
Enrollment
Unknown
Registered
2019-03-24
Start date
2019-04-01
Completion date
Unknown
Last updated
2019-06-17

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

Conditions

esophageal cancer

Interventions

Group1:chemoradiotherapy
Group 2:Endostar Combined with chemoradiotherapy
Group 3:Hyperthermia Combined with chemoradiotherapy
Group 4:Endostar and hyperthermia Combined with chemoradiotherapy

Sponsors

The Second Affilicated Hosptical of Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-65 years, male or female; 2. Histopathologically confirmed esophageal squamous cell carcinoma and esophageal adenocarcinoma; 3. Clinical stage II to IVa; 4. Karl's score (> 70); 5. There are measurable lesions (RECIST version 1.1); 6. This treatment must be the first course of treatment; 7. Expected survival =6 months; 8. Laboratory inspections meet the following requirements: WBC = 4.0×10^9/L, neutrophil count = 2.0×10^9/L, PLT = 100×10^9/L; total bilirubin, ALT, AST = 1.25 times the upper limit of normal; PT is within the upper limit of normal value. 9. Participants voluntarily joined the study, signed informed consent; 10. Participants had good compliance and follow-up.

Exclusion criteria

Exclusion criteria: 1. Have a distant metastasis; 2. History of malignancy in other sites; 3. Chemotherapy and chest radiotherapy before the start of the trial; 4. Radiotherapy and chemotherapy contraindications include severe infections or other complications such as myocardial infarction, severe arrhythmia, severe cerebrovascular disease, psychosis and uncontrollable diabetes mellitus; 5. Received target therapies; 6. Haemorrhagic tendencies; 7. There is tracheoesophageal fistulas.

Design outcomes

Primary

MeasureTime frame
Objective response rate;disease control rate;progression-free survival;Overall survival;

Secondary

MeasureTime frame
drug safety;Liver and kidney function;

Countries

China

Contacts

Public ContactLiu Wenqi

The Second Affilicated Hosptical of Guangxi Medical University

2538613851@qq.com+86 0771-3276313

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026